Curriculum Vitae

Helen Donis-Keller, Ph.D.

Art and Science Curriculum Vitae

August 2014

Post-Secondary Education and Degrees Granted:

1998-2001 Master of Fine Arts (Studio Art), School of the Museum of Fine Arts and Tufts University, Boston and Medford, MA
May, 1995 Doctor of Science Degree (Honoris Causa), Lakehead University, Thunder Bay, Ontario
1979-1981 Helen Hay Whitney Postdoctoral Fellowship, Harvard Medical School, Boston, MA
1975-1979 Ph.D. in Biochemistry and Molecular Biology, Harvard University, Cambridge, MA
Thesis Title: “Enzymatic RNA Sequencing and Fractionation Methods”
Thesis Advisor: Walter Gilbert
1973-1975 Honours Bachelor of Science in Biology (First Class Standing), Lakehead University, Thunder Bay, Ontario
1971-1973 Bachelor of Science in Natural Science (First Class Standing), Lakehead University, Thunder Bay, Ontario
1965-1969 Major in Graphic Design, University of Cincinnati,
School of Design, Architecture, and Art, Cincinnati, OH

Professional Positions (since 1980):

11/12 – Present Appointed Michael E. Moody Professor, Franklin W. Olin College of Engineering, Needham, MA
9/01-Present Professor of Biology and Art, Franklin W. Olin College of Engineering, Needham, MA

Teaching:
Bacteriophage Genomics Research Project Laboratory (SCI 3100), The Digital Eye (AHS 1135), Principles of Modern Biology with Laboratory: Human Genetics and Genomics  (SCI 1210), Seeing and Hearing: communication using photography, video and sound (AHSE 1130), Six Experiments that Changed the World (SCI 2099), Independent Study in Biology, Responsive Drawing and Visual Thinking (AHSE 2131), Independent Study in Drawing, The Intersection of Art and Science (AHSE 2130), Advanced Digital Photography (AHSE 3130), Human Genetics in the Age of Genomics (SCI 3210), User Oriented Collaborative Design (ENGR 2250)

Service on College Committees (current):
Faculty Representative to Board of Trustees, Facilities, and Finance Committee; Chair, Mathematics and Science Field Group; Member, Art in Public Spaces Committee; Curator, Olin Art Gallery; Member, Arts Humanities and Social Sciences Committee; Numerous Faculty Search Committees

Current Science Research:
Identification and characterization of genomes of bacteriophages of M. smegmatis; Geometric Reasoning, Spatial Visualization, and Drawing by undergraduates in STEM and non-STEM concentrations

Art Focus:
Art inspired by research experience in science; media is often photo-based also employ drawing, video, printmaking, acrylic painting, sound

10/92-6/01 Professor of Surgery and Director, Division of Human Molecular Genetics, Department of Surgery; Joint Appointments – Professor of Genetics, Dept. of Genetics; Professor of Genetics in Psychiatry, Psychiatry Department, Washington University School of Medicine, St. Louis, MO (on leave 9/98-6/01)
2/89 – 9/92 Professor of Genetics, Department of Genetics, Professor of Genetics in Psychiatry, Department of Psychiatry, Washington University School of Medicine, St. Louis, MO
1/83 – 1/89 Director Department of Human Genetics, Collaborative Research, Inc.
Waltham/Lexington/Bedford, MA
5/80 – 12/82 Assistant Research Director of Molecular Biology, Biogen, Inc., Cambridge, MA

Science Awards:

  • CaPCURE Foundation Prostate Cancer Research Award, 1996
  • Doctor of Science Degree (Honoris Causa), Lakehead University, Thunder Bay, Ontario, 1995
  • Marion Spencer Fay National Board Award of the Medical College of Pennsylvania, 32nd Annual Award, 1994
  • Helen Hay Whitney Postdoctoral Fellowship, 1979
  • Dean of Science Medal, Lakehead University, 1975
  • Lieutenant Governor’s Medal (Canada), Lakehead University, 1973

Art and Science Invited Lectures, Panel Discussions, Art Awards (selected)

  • Seminar Speaker, “Coming Full Circle: My Life in Art and Science”, sponsored by the Art of Science/Women in Science Series at Brandeis University, November 5, 2012
  • Session Leader and Speaker for Workshop I “Designing and Printing Digital Fine Art Photography Books”, Digital Book Summit, Sponsored by Olin College and the Society for the Contemporary Book, at Olin College, October 13, 2012
  • Seminar Speaker, “The Portfolio Project: Helping Students take more responsibility for their learning”, sponsored by HHMI/MITBiology Education Group, March 7, 2012
  • Visiting Class Lecture, “Encounters with the Elements: Death Valley and Iceland”, invited talk to Wellesley College Art Department, photography class of David Kelley, February 23, 2012
  • Runner-up Award, 3rd Quarter, Forward Thinking Museum 2011 Photography Contest Artist Level, 2011
  • Seminar Speaker, “The Intersection of Art and Science: Do They Inform Each Other?” Sponsored by Needham Community Education, Olin College, December 2, 2010
  • Speaker, Liberal Arts Division ASEE, “A Course in Communication and Creativity for Undergraduates in Engineering: Seeing and Hearing: Communicating with Photographs, Video and Sound”, 2009 American Society for Engineering Education Annual Meeting, Austin, TX, June 14 – June 17, 2009
  • Seminar Speaker, “Ethical Implications of Genetic Testing in the 21st Century”, Franklin and Marshall College, Lancaster, PA, March 8, 2007
  • Seminar Speaker, “The Intersection of Art and Science”, Institute for Genomic Sciences, Universidad Nacional Autónoma de México, Mexico, Cuernavaca, via videoconference, November 4, 2005
  • Seminar Speaker, “Coming Full Circle”, Cold Spring Harbor Laboratory Symposium in Honor of Walter Gilbert, June 22, 2005
  • Seminar Speaker, “The Intersection of Art, Science, and Engineering at Olin College”, MIT, HHMI Education Seminar Series, Biology Department, Cambridge, MA, May 12, 2005
  • Gallery Talk, “Genetic Passages: The Genotype:Phenotype Portraits of Helen Donis-Keller”, Midwest Museum of Art, Elkhart, IN, September 14, 2003
  • Biology Colloquium Speaker, University of Wisconsin-Milwaukee, “Art, Science, and the Creative Process”, Milwaukee, WI, April 25, 2003
  • Keynote Speaker, “Creativity in Art and Science”, Indiana Association for Institutional Research (INAIR) Annual Meeting, April 3, 2003
  • Panel Discussion Member and Speaker, Genomic Issues: Art and Science Exhibition, City University of New York (CUNY), New York, NY, March 14, 2003
  • Session Chair, “Audio in Undergraduate Education”, Art and Science Collaboration, Inc. (ASCI) 2002, New York, NY, December 8, 2002
  • Gallery Talk, “Near at Hand”, Exhibition at Horn Gallery, Babson College, Wellesley, MA, September 19, 2002
  • Gallery Talk, Thesis Exhibition, Tufts Art Gallery, Medford, MA, May 3, 2001
  • Music Credit (excerpts from Erehwon Variations 1999) and on-camera interview.
  • Paradise Now – Picturing the Genetic Revolution, a video by Kathy Brew and Roberto Guerra from Mosquito Productions. Exhibited at Exit Art, New York, NY., September 9 – October 19, 2000
  • Boit Competition Jury Prize, Boit Exhibition 2000, (Video documentary: Altered Flats – The Paintings of Bill Thompson) School of the Museum of Fine Arts, Boston, MA, October 2000
  • Special Merit Award Essex Art Center Sixth Annual Juried Show, Lawrence, MA, October 1999
  • Participant, Panel Discussion on Art and Science at the Millennium, Organized by Charles H. Traub, School of Visual Arts, and sponsored by Howard Stein, New York, NY, June 1998
  • Clay Eugene Jordan Annual Bequest Prize for Photography, St. Louis Artists Guild, October 1996
  • Speaker, Panel Participant, Dialogues: Art and Science Symposium, Washington University, School of Art, September 21, 1996
  • Speaker, MIT Biology Department Colloquia, April 23, 1996
  • Speaker, University of Southern California Human Genetics Institute, Los Angeles, February 21, 1996
  • Commencement Speaker, University of Vermont Medical School, May 20, 1995
  • Keynote Speaker, Colloquium “Molecular Approaches to Human Disease”, sponsored by Univ. N. Texas and Texas Women’s Univ., Denton, TX, April 21, 1995
  • Keynote Speaker, National Conference: The New Genetics and Its Impact on Women, University of Chicago, March 10, 1995
  • Speaker, Executive Institute for Advanced Study, Challenges in the 21st Century: Genetic Information, the Genome Project, and Society. Washington University, December 1, 1994
  • Speaker, 1994 National Association of Biology Teachers, St. Louis, MO, November 17, 1994
  • Panelist and Workshop Chair, Public Responsibility in Medicine and Research (PRIMR) conference: Educating for the Responsible Conduct of Research, Boston, MA, November 2 – November 4, 1994
  • Speaker and Co-chairperson session on databases, NIH sponsored meeting “Breast Cancer Resources to Facilitate Research” Washington, DC, September 21, 1994
  • Chairperson and Speaker, Session on Breast Cancer: Molecular Genetics and Predictive Testing. American Society of Clinical Oncologists, Annual Meeting, Dallas TX, May 14, 1994
  • Lectureship, Sigma Xi, The Scientific Research Society, Roche Research Chapter. Nutley New Jersey, November 3, 1993

Interviews/Reviews and Publications on Art (1996 – 2014):

  • Wrote “Foreword” to John Wawrzonek’s book, “The Hidden World of the Nearby: Catalog of the Exhibition at Olin College”, 2014
  • Interview on my experiences in the biotechnology industry for the Life Sciences Foundation history project, September 2013
  • Interview on Reflections on Educational Experience at Lakehead University, “Remembering Lakehead: alumni share their memories” Appears in Lakehead University Magazine, 2005. Vol. 22 (1) pg. 8.
  • Interview on Art and Teaching “Alumni art making enriches lives and strengthens communities: the artist as teacher” Appears in ArtMatters, Fall 2003, pgs 3-5.
  • Painting Neurology #4 and commentary featured in “Work and lives in progress”, ArtMatters, Spring 2003, pgs. 1-16.
  • Interview/Review of exhibition “Genetic Passages: the Genotype/Phenotype Portraits of Helen Donis-Keller”, Appears in The Truth, Arts Section, “Heading into Infinity” by Marcia Fulmer, issue September 4, 2003
  • Interview/Review of exhibition “Near at Hand”, Appears in the newspaper The Wellesley Townsman, Wellesley Life section, “The Science and Business of Art” by Lesley Mahoney, issue September 19, 2002
  • Interview on Art and Engineering. Appears in The Chronicle of Higher Education “The Fine Art of Engineering” by Peter Monaghan. Notes from Academe Section, August 2, 2002. Vol.XLVIII: No47
  • Interview on Art and Science. Appears in Picturing DNA (Chapter 4, Who Owns your Genes?) by Bettyann Holtzmann Kevles and Marilyn Nissensen, 2000, See www.geneart.com chap4.htm
  • Interview on Art, Science, and Life. Appears in St. Louis Post Dispatch, “Portraits of St. Louis, Helen Donis-Keller”, by Monte Reel, photos by J.B. Forbes, Section D cover, pgs D8-9, June 28, 1998
  • Interview, National Public Radio program, Talk of the Nation: Science Friday, with I. Flatow, C. Wagner, and H. Longino, Art and Science: Investigating Matter, October 25, 1996

Exhibitions (1996 – 2014):

  • The Consilience of Art and Science, January 10 – February 28, 2014, Pence Gallery, Davis, CA, sponsored by Tandem Properties and UC Davis Art/Science Fusion program,
  • The Annual AIDS Benefit Exhibition, December 7 – 11, 2013, Barbara Krakow Gallery, Boston, MA,
  • The Annual AIDS Benefit Exhibition, December 1 – 8, 2012, Barbara Krakow Gallery, Boston, MA,
  • School of the Museum of Fine Arts Exhibition and Sale, November 29 – December 2, 2012, Boston, MA
  • The Annual AIDS Benefit Exhibition: EVERYTHING BUT PAPER PRAYERS, December 10 – 17, 2011, Barbara Krakow Gallery, Boston, MA
  • Inside Out: School of the Museum of Fine Arts Exhibition and Sale, December 8 – 11, 2011, Boston, MA
  • Encounter with the Elements, an exhibition of photographs: Iceland and Death Valley, Solo Exhibition, September 23 – November 5, 2011, LaCapelli Salon and Gallery, Cambridge, MA
  • The Annual AIDS Benefit Exhibition: EVERYTHING BUT PAPER PRAYERS, December 11 – 18, 2010, Barbara Krakow Gallery, Boston, MA
  • The Annual AIDS Benefit Exhibition: EVERYTHING BUT PAPER PRAYERS, November 28 – December 17, 2009, Barbara Krakow Gallery, Boston, MA.
  • InsideOut: School of the Museum of Fine Arts Exhibition and Sale, November 18 – 22, 2009, Boston, MA
  • The Annual AIDS Benefit Exhibition: Everything but Paper Prayers, November 29 – December 17, 2008, Barbara Krakow Gallery, Boston, MA.
  • School of the Museum of Fine Arts Exhibition and Sale, November 19-23, 2008
  • Commonwealth School 50th Anniversary Art Exhibition at the Cyclorama, Boston Center for the Arts, Boston, October, 2008
  • The Annual AIDS Benefit Exhibition: Everything but Paper Prayers, December 1 – 19, 2007, Barbara Krakow Gallery, Boston, MA.
  • School of the Museum of Fine Arts Exhibition and Sale, December, 2007
  • Drawn In, Group Exhibition, May 14 – June 29, 2007, Arlington Center for the Arts, Gibbs Gallery, Arlington, MA
  • School of the Museum of Fine Arts Exhibition and Sale, December, 2006
  • The Annual AIDS Benefit Exhibition: Everything but Paper Prayers, December 2 – 19, 2006, Barbara Krakow Gallery, Boston, MA.
  • Proof of Purchase, Group Exhibition, September 2006, RHYS Gallery, Boston, MA.
  • The Annual AIDS Benefit Exhibition: Everything but Paper Prayers, December 3 – 20, 2005, Barbara Krakow Gallery, Boston, MA.
  • Pediatric AIDS Benefit Exhibition, December 4 – December 18, 2004, Barbara Krakow, Gallery, Boston, MA
  • Pediatric AIDs Benefit Exhibition, November 29 – December 20, 2003, Barbara Krakow Gallery, Boston, MA
  • Genetic Passages: The Genotype/Phenotype Portraits of Helen Donis-Keller, Solo Exhibition, September 5 – Oct 12, 2003, The Midwest Museum of Art, Elkhart, IN, In conjunction with the Michiana Museum Consortium Project, “Exhibiting Identity”
  • Genomic Issues: Art and Science, Group Exhibition, February 25 – April 5, 2003, City University of New York Gallery, New York, NY
  • Pediatric AIDs Benefit Exhibition, November 30 – December 21, 2002, Barbara Krakow Gallery, Boston, MA
  • PhotoGENEsis: Opus 2 Group Exhibition, November 9, 2002 – February 9, 2003, Santa Barbara Museum of Art, Santa Barbara, CA
  • Near at Hand: Work by Arts Faculty at Babson College and Franklin W. Olin College of Engineering, September 19 – October 17, 2002, Horn Gallery, Babson College, Wellesley, MA
  • Butler Museum of Art, Youngstown OH, 2002- continuous exhibition of video documentary, “Altered Flats – the Paintings of Bill Thompson”
  • December Group Exhibit and Sale, 2001, 2002, Sorensen Art Center Gallery, Babson College, Wellesley, MA
  • Portraiture of the 21st Century, Group Exhibition, June 18, 2001 – September 7, 2001, University of California, Santa Cruz, CA
  • MFA Thesis Exhibition, Genetic Passages, May 3, 2001 – May 20, 2001
    • School of the Museum of Fine Arts, Boston, Tufts University, Medford, MA.
    • Tufts University Gallery, Medford, MA
  • Film and Video Annual 2001, April 26, 2001 and May 5, 2001, Museum of Fine Arts, Boston, MA
  • Boit Exhibition 2000, September 22 – October 8, 2000, School of the Museum of Fine Arts, Boston, MA
  • MFA Exhibition, September 22 – October 4, 2000, School of the Museum of Fine Arts, Boston, MA
  • Film and Video Annual 2000, April 27, 2000, Museum of Fine Arts, Boston, MA
  • Graduate Student Group Exhibition, October 1998, School of the Museum of Fine Arts, Boston, MA
  • Essex Art Center Sixth Annual Juried Show 1999, October 22 – November 30, 1999, Lawrence, MA
  • Second Year MFA Graduate Student Exhibition, October 22 – November 14, 1999, School of the Museum of Fine Arts, Boston, MA
  • United Airlines First Class Lounge Gallery Group Exhibition, July 1 – November 1, 1999, Boston, MA
  • Vid-e-o Exhibition, October 1998, School of the Museum of Fine Arts, Boston, MA
  • Center for Photography Gallery, Group Exhibition, September 1997, St. Louis, MO
  • St. Louis Artists’ Guild Prints, Drawings and Pastels, Group Exhibition, May 15 – June 21, 1997, St. Louis, MO
  • Washington University Medical School Faculty Art Show, Group Exhibition June 1994, June 1995, June 1997 St. Louis, MO
  • St. Louis Artists’ Guild Membership Juried Exhibition, Group Exhibition, October 20 – November 13, 1996, Clayton, MO
  • St. Louis Artists’ Guild Photography Exhibition, Group Exhibition, September 15 – October 11,1996, Clayton, MO

Curatorial/Gallery Organizational Work

2014 Organized with John Wawrzonek a solo exhibition of his fine art photography, The Hidden World of the Nearby, February 20 – June 1, 2014, Olin College Art Gallery, Olin College of Engineering, Needham, MA
2013 Organized with students as a co-curricular activity, an Olin Student Photography Exhibit, Spring 2013, Olin College Art Gallery, Olin College of Engineering, Needham, MA
2009 Organized solo exhibition of work of Mark Green, April 16 – May 29, 2009, Olin College Art Gallery, F.W. Olin College of Engineering, Needham, MA
2007 Organized solo exhibition of work of Erica Daborn, Interplay: A Painter’s Dialogue with Photography, February 22 – March 31, 2007, Olin College Art Gallery, F.W. Olin College of Engineering, Needham, MA
2006 Helped organize and served on jury of two exhibitions at Olin College: Member of Jury, Inaugural Exhibition of the Olin Art Gallery, February, 2006, F. W. Olin College of Engineering, Needham, MA
Member of Jury, Student Art Exhibition, May, 2006, Olin Art Gallery, F.W. Olin College of Engineering, Needham, MA

Representation in Museums and other Institutions

  • Twelve Phenotype Series Images, Villains Falls Panoramic photograph, Neurology series paintings on loan to Olin College, displayed in Executive Suite Offices
  • Three Phenotype Series 2003 works, Collection of the Danforth Museum, Framingham, MA
  • Genetic Portrait 2003, Collection of the Midwest Museum of American Art, Elkhart, IN
  • Genotype:Phenotype Wall Piece 2001, Joy of Giving Something (JGS) Foundation, New York, NY
  • Video documentary “Altered Flats – The Paintings of Bill Thompson,” in conjunction with exhibition of the work of Bill Thompson, Butler Museum of Art, Youngstown, OH

Science and Art Teaching (2001 – 2014):

  • Developed and taught the following courses at Franklin W. Olin College of Engineering:
    • SCI 1210-02 (Foundation course required for all undergraduates) Principles of Modern Biology with Laboratory: Human Genetics and Genomics
    • AHSE 1130 (Foundation Course, one of which is required for all undergraduates) Seeing and Hearing: communication with photography, video and sound
    • AHSE 1135 (Foundation Course, one of which is required for all undergraduates)
      The Digital Eye
    • AHSE 2130 The Intersection of Art and Science
    • AHSE 2131 Responsive Drawing and Visual Thinking
    • SCI 3100 (previously 2299) Bacteriophage Genomics Research Project Laboratory
    • AHSE 3130, Advanced Digital Photography
    • SCI 3210, Human Molecular Genetics in the Age of Genomics, F.W. Olin College of Engineering, 9/05 – present
  • Co-Developed and Co-Taught, SCI 2099, Six Experiments that Changed the World (I developed and taught two of the four topics, i.e. Mendel and the Foundation of Genetics and DNA sequencing Method Development
  • Co-Taught, ENG 2250 User Oriented Collaborative Design (UOCD)
  • Mentor, Olin Self-Study Projects and Independent Study Projects in Science and Art

Websites with Science or Art Content by HDK

Publications

Journal Articles

  • Hatfull, G.F., D. Jacobs-Sera, J.G. Lawrence, W.H. Pope, D.A. Russell, C-C. Ko, R.J. Weber, M.C. Patel, K.L. Germane, R.H Edgar, N.N. Hoyte, C.A. Bowman, A.T.Tantoco, E.C. Paladin, M.S. Myers, A.L. Smith, M.S. Grace, T.T. Pham, M.B. O’Brien, A.M. Vogelsberger, A.J. Hryckowian, J.L. Wynalek, H. Donis-Keller, M.W. Bogel, C.L. Peebles, S.G. Cresawn, R.W. Hendrix (2010). Comparative Genomic Analysis of 60 Mycobacteriophage Genomes: Genome clustering, Gene Acquisition and Gene Size. Journal of Molecular Biology, 397(1): 119 – 143.
  • Donis-Keller, H. (2009). A Course in Communication and Creativity for Undergraduates in Engineering: Seeing and Hearing: Communicating with Photographs, Video and Sound. 2009 American Society for Engineering Education Annual Meeting, June 14-17, Austin, TX, DVD meeting publication.
  • Somerville, M., D. Anderson, H. Berbeco, J.R. Bourne, J. Crisman, D. Dabby, H. Donis-Keller, S. Holt, D.V. Kerns, Jr., S.E. Kerns, R. Martello, R.K. Miller, M. Moody, G. Pratt, J.C. Pratt, C. Shea, S. Schiffman, S.Spence, L.A. Stein, J.D. Stolk, B.D. Storey, B. Tilley, B. Vandiver, and Y. Zastavker (2005). The Olin Curriculum: Thinking toward the future. IEEE Transactions on Education, 48(1): 198 – 205.
  • Oriola, J., I. Halperin, F. Rivera-Fillat, and H. Donis-Keller (2002). The finding of a somatic deletion in RET exon 15 clarified the sporadic nature of a medullary thyroid carcinoma suspected to be familial. Journal of Endocrinology Investigation, 25(1): 25-31.
  • Glass, A.G., H. Donis-Keller, C. Mies, J. Russo, B. Zehnbauer, S. Taube, and R. Aamodt (2001). The Cooperative Breast Cancer Tissue Resource: archival tissue for the investigation of tumor markers. Clinical Cancer Research, 7: 1843-1849.
  • Ghiasvand, N.M., A.B. Kanis, C. Helms, V.C. Sheffield, E.M.Stone, and H. Donis-Keller (2000). Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21. American Journal of Medical Genetics, 90(2): 165-168.
  • Ghiasvand, N.M., T.P. Fleming, C. Helms, A. Avisa, and H. Donis-Keller (2000). Genetic fine mapping of the gene for nonsyndromic congenital retinal nonattachment. American Journal of Medical Genetics, 92(3): 220-223.
  • Wang, J.C., D.M. Radford, M.S. Holt, C. Helms, A. Goate, W. Brandt, M. Parik, N.J. Phillips, K. DeSchryver, M.E. Schuh, K.I. Fair, J. H. Ritter, P. Marshall, and H. Donis-Keller (1999). Sequence-ready contig for the 1.4-cM ductal carcinoma in situ loss of heterozygosity region on chromosome 8p22-p23. Genomics, 60(1): 1-11.
  • Doll, J.A., X. Zhu, J. Furman, Z. Kaleem, C. Torres, P.A. Humphrey, and H. Donis-Keller (1999). Genetic analysis of prostatic atypical adenomatous hyperplasia (adenosis). American Journal of Pathology, 155(3): 967-971.
  • Urban, Z., V.V. Michels, S.N. Thibodeau, H. Donis-Keller, K. Csiszar, and C.D. Boys (1999). Supravalvular aortic stenosis: a splice site mutation within the elastin gene results in reduced expression of two aberrantly spliced transcripts. Human Genetics, 104(2): 135-142.
  • Bacher, J.W., J.W. Schumm, C. Helms, and H. Donis-Keller (1999). Chromosome localization of codis loci and new pentanucleotide repeat loci. Proceedings of the 18th International ISFH Congress
  • Bacher, J.W., L.F. Hennes, T. Gu, A. Tereba, K.A. Micka, C.J. Sprecher, A.M. Lins, E. A. Amiott, D.R. Rabbach, J. A. Taylor, C. Helms, H. Donis-Keller, and J.W. Schumm (1998). Pentanucleotide Repeats: highly polymorphic genetic markers displaying minimal stutter artifact. Proceedings from the Ninth International Symposium on Human Genetics pgs 24-37.
  • Inoue, H., Y. Tanizawa, J. Wasson, P. Behn, K. Kalidas, E. Bernal-Mizrachi, M. Mucckler, H. Marshall, H. Donis-Keller, P. Crock, D. Rogers, M. Mijuni, H. Kumashira, K. Higashi, G. Sobue, Y. Oka, and M. A. Permutt (1998). A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome). Nature Genetics, 20(2): 143-148.
  • Ferrer, J., J. Wasson, K.D. Schoor, M. Mueckler, H. Donis-Keller, and M.A. Permutt (1997). Mapping novel pancreatic islet genes to human chromosomes. Diabetes, 46(3): 386-392.
  • Inoue, H., A. Rudnick, M. S. German, R. Veile, C. Helms, H. Donis-Keller, and M. A. Permutt (1997). Isolation, characterization, and chromosomal mapping of the human Nkx6.1 gene, a new pancreatic islet homeobox gene. Genomics, 40: 367-370.
  • Pandit, S. D., T. O’Hare, H. Donis-Keller, and L. J. Pike (1997). Functional characterization of an epidermal growth factor receptor/RET chimera. Journal of Biological Chemistry, 272: 2199-2206.
  • Aoki, M., L. Koranyi, A. C. Riggs, J. Wasson, K. C. Chiu, M. Vaxilllaire, P. Froguel, S. Gough, L. Liu, H. Donis-Keller, and M. A. Permutt (1997). Identification of trinucleotide repeat containing genes in human pancreatic islets. Diabetes, 45(6): 789-794.
  • Iannotti, C.A., H. Inoue, E. Bernal, M. Aoki, L. Liu, H. Donis-Keller, M.S. German, and M.A. Permutt (1997). Identification of a human LMX1 (LMX1.1)-related gene, LMX1.2: tissue-specific expression and linkage mapping on chromosome 9. Genomics, 46(3): 520-524.
  • Morton, S. M., R. A. Veile, C. Helms, M. Lee, W-L. Kuo, J. Gray, and H. Donis-Keller (1997). Subregional localization of 23 chromosome 7-specific expressed sequence tags (ESTs) by FISH using newly identified YACs and P1s. Genomics, 46:491-494.
  • Doll, J. A., B. K. Suarez, and H. Donis-Keller (1996). Association between prostate cancer in Black Americans and an allele of the PADPRP pseudogene locus on chromosome 13. American Journal of Human Genetics, 58:425-428.
  • Inoue, H., A.C. Riggs, Y. Tanizawa, K. Ueda, A. Kuwano, L. Liu, H. Donis-Keller, and M.A. Permutt (1996). Isolation, characterization, and chromosomal mapping of the human insulin promoter factor 1 (IPF-1) gene. Diabetes, 45(6): 789-794.
  • Phillips, N. J., M. Ziegler, D. M. Radford, K. L. Fair, T. Steinbrueck, F. P. Xynos, and H. Donis-Keller (1996). Allelic deletion on chromosome 17p13.3 in early ovarian cancer. Cancer Research 56: 606-611.
  • Pandit, S., H. Donis-Keller, J. Tomich, and L. Pike (1996). The MEN 2B mutation alters long term regulation and enhances the transforming capacity of the EGF receptor. Journal of Biological Chemistry, 271(10): 5850-5858.
  • White, G. R. M., M. Stack, M. Santibanez-Koref, D. S. Liscia, T. Venesio, J-C. Wang, C. Helms, H. Donis-Keller, D. C. Betticher, H. J. Altermatt, P. R. Hoban, and J. Heighway (1996). High levels of loss at the 17p telomere suggest the close proximity of a tumour supressor. British Journal of Cancer, 74: 863-870.
  • Belloni, E., M. Muenke, E. Roessler, G. Traverso, J. Siegel-Bartelt, A. Frumkin, H. f. Mitchell, H. Donis-Keller, C. Helms, A. V. Hing, H. H. Q. Heng, B. Koop, D. Martindale, J. M. Rommens, L. C. Tsui , and S. W. Scherer (1996). Identification sonic-hedgehog as a candidate gene responsible for holoprosencephaly. Nature Genetics, 14: 353-356.
  • Urban, Z., C. Helms, G. Fekete, K. Csiszar, D. Bonnet, A. Munnich, H. Donis-Keller, and C. D. Boyd (1996). 7q11.23 deletions in Williams syndrome arise as a consequence of unequal meiotic crossing over. American Journal of Human Genetics, 59: 958-962.
  • Vocero-Akbani, A., C. Helms, J-C. Wang, F. J. Sanjurjo, J. Korte-Sarfaty, R. A. Veile, L. Liu, A. Jauch, A. K. Burgess, A. Hing, M. S. Holt, S. Ramachandra, A. J. Whelan, R. Anker, L. Ahrent, M. Chen, M. R. Gavin, K. Iannantuoni, S. M. Morton, S. D. Pandit, C. M. Read, T. Steinbrueck, C. Warlick, D. A. Smoller, and H. Donis-Keller (1996). Mapping human telomere regions with YAC and P1 clones: Chromosome specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regions. Genomics, 36: 492-506.
  • Schrock, E., G. Thiel, T. Lozanova, S. SuManoir, M-C. Meffert, A. Jauch, M. R. Speicher, P. Nurnberg, S. Vogel, W. Janisch, H. Donis-Keller, T. Ried, , R. Witkowski, and T. Cremer (1995). Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and non-random chromosomal gains and losses. American Journal of Pathology, 144: 1203-1218.
  • L.C. Tsui, H. Donis-Keller, and K.H. Grzeschik (1995). Report of the second international workshop on human chromosome 7 mapping 1994. Cytogenet ics and Cell Genetics, 71(1): 2-21.
  • Glaser, B., K. C. Chiu, L. Liu, R. Anker, A. Nestorowicz, N. J. Cox, H. Landau, N. Kaiser, P. A. Thornton, C. A. Stanley, E. Cerasi, L. Baker, H. Donis-Keller, and M. A. Permutt (1995). Recombinant mapping of the Familial Hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews. Human Molecular Genetics, 4: 879-886.
  • Litt, M., P. Kramer, E. Kort, P. Fain, S. Cox, D. Root, R. White, J. Weissenbach, H. Donis-Keller, R. Gatti, J. Weber, Y. Nakamura, C., Julier, K. Hayashi, N. Spurr, M. Dean, J. Mandel, K. Kidd, T. Kruse, A. Retief, A. Bale, T. Meo, G. Vergnaud, S. Warren, and H. F. Willard (1995). The CEPH consortium linkage map of human chromosome 11. Genomics, 27: 101-112.
  • Kitamoto, Y., Veile, R.A., Donis-Keller, H., and J. E. Sadler (1995). cDNA sequence and chromosomal localization of human enterokinase, the proteolytic activator of trypsinogen. Journal of Biochemistry, 34: 4562-4568.
  • Kozman, H.M., T.P. Keith, S. Gerken, H. Donis-Keller, R. L. White, J. Weissenbach, M. Dean, G. Vergnaud, K. Kidd, J. Gusella, A. Jeffreys, G.R. Sutherland, and J. C. Mulley (1995). The CEPH consortium linkage map of human chromosome 16. Genomics, 25: 44-58.
  • Radford, D. M., K. L. Fair, N. J. Phillips, J. H. Ritter, T. Steinbrueck, M. S. Holt, and H. Donis-Keller (1995). Allotyping of ductal carcinoma in situ (DCIS) of the breast: deletion of loci on 8p, 13q, 16q, 17p, and 17q. Cancer Research, 55: 3399-3405.
  • Tsui, L-C, H. Donis-Keller, and K-H Grzeschik (1995). Report of the Second International Workshop on human chromosome 7 mapping 1994. Cytogenetics and Cell Genetics, 71: 2-31.
  • Hing, A. V., C. Helms, R. Slaugh, A. Burgess, J. C. Wang, T. Herman, S. B. Dowton, and H. Donis-Keller (1995). Linkage of preaxial polydactyly type 2 to 7q36. American Journal of Medical Genetics, 58: 128-135.
  • Cox, D. W., G. D. Billingsley, A. E. Bale, Cooperative Human Linkage Center, H. Donis-Keller, J. H. Edwards, M. Litt, W. McBride, F. Persichetti, N. K. Spurr, J. L. Weber, J. Weissenbach, and R. White (1995). CEPH consortium map of Chromosome 14. Cytogenetics and Cell Genetics, 69:175-178.
  • Pandit, S. D., J. C. Wang, R. A. Veile, S. K. Mishra, C. A. Warlick, and H. Donis-Keller (1995). Index, comprehensive microsatellite, and unified linkage maps for human chromsome 14 with cytogenetic tie points and a telomere microsatellite marker. Genomics, 29: 653-664.
  • Radford, D. M., M. S. Holt, J. H. Ritter, N. J. Phillips, K. L. Fair, K. DeSchryver, E. Schuh, and H. Donis-Keller (1995). Allelic Loss on chromosome 8p occurs early in the development of breast carcinoma. Surgical Forum, 46: 553-535.
  • Donis-Keller (1995). The RET protooncogene and Cancer. Journal of Internal Medicine, 238: 319-325.
  • Cox, S., S. P. Bryant, A. Collins, J. Weissenbach, H. Donis-Keller, P. H. Reitsma, A. Steunjasserer, and N. K. Spurr (1995). Integrated gene map of human chromosome 2. Annals of Human Genetics, 59: 413-434.
  • Radford, D. M., N. J. Phillips, K. L. Fair, J. H. Ritter, M. Holt, and H. Donis-Keller (1995). Allelic loss and the progression of breast cancer. Cancer Research, 55: 5180-5183.
  • Attwood, J., M. Chiano, A. Collins, H. Donis-Keller, N. Dracopoli, J. Fountain, C. Falk, D. Goudie, J. Gusella, J. Haines, J. L. Armour, A. Jeffreys, D. Kwiatkowski, M. Lathrop, T. Matise, H. Northrup, M. A. Pericak-Vance, J. Phillips, A. Retief, E. Robson, D. Shields, S. Slaugenhaupt, G. Vergnaud, J. Weber, J. Weissenbach, R. White, J. Yates, and S. Povey (1994). CEPH consortium map of chromosome 9. Genomics, 19: 203-214.
  • Carlson, K. M., S. Dou, D. Chi, N. Scavarda, K. Toshima, C. E. Jackson, S. A. Wells, Jr., P. J. Goodfellow, and H. Donis-Keller (1994). A single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is asociated with multiple endocrine neoplasia type 2B. Proceedings of the National Academy of Science, USA, 91: 1579-1583.
  • Lindberg, F. P., D. M. Lublin, M. J. Telen, R. A. Veile, Y.E. Miller, H. Donis-Keller, and E.J. Brown (1994). Rh-related antigen CD47 is the signal-transducer integrin associated protein. Journal of Biological Chemistry, 269:1567-1570.
  • Wells, S. A. Jr. and H. Donis-Keller (1994). Current perspectives on the diagnosis and management of patients with the multiple endocrine neoplasia type 2 syndromes. Endocrinology and Metabolism Clinics of North America, 23:215-228.
  • Glaser, B., K. C. Chiu, R. Anker, A. Nestorwicz, H. Landau, H. Ben-Bassat, Z. Shlomai, N. Kaiser, P. S. Thornton, C. A. Stanley, R. S. Spielman, K. Gogolin-Ewens, E. Cerasi, L. Baker, J. Rice, H. Donis-Keller, and M. A. Permutt (1994). Familial hyperinsulinism maps to 11p14-15.1 30cM centromeric to the insulin gene. Nature Genetics, 7:185-188.
  • Carlson, K. M., S. Dou, K. Toshima, D. Chi, and H. Donis-Keller (1994). Three dinucleotide repeat polymorphisms closely linked to the RET protooncogene D10S1098, D10S1099 and D10S1100. Human Molecular Genetics, 3:1207.
  • Ott, J. and H. Donis-Keller (1994). Statistical methods in genetic mapping: meeting report. Genomics, 22: 496-497.
  • Tanizawa, Y., A. C. Riggs, S. C. Elbein, A. Whelan, H. Donis-Keller, and M. A. Permutt (1994). Human Glucagon-like peptide-1 receptor gene in non-insulin dependent diabetes mellitus: identification and use of simple sequence repeat polymorphisms in genetic analysis. Diabetes, 43:752-757.
  • Chi, D. D., K. Toshima, S. A. Wells, Jr., and H. Donis-Keller (1994). Predictive testing for Multiple Endocrine Neoplasia type 2A based on the detection of mutations in the RET protooncogene. Surgery, 116: 124-133.
  • Wells, S. A., Jr., D. D. Chi, K. Toshima, L. P. Dehner, C. M. Coffin, S. B. Dowton, J. L. Ivanovitch, M. K. DeBenedetti, J. F. Moley, and H. Donis-Keller (1994). Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A. Annals of Surgery, 220: 237-250.
  • Haltia, M., M. Vitaanen, R. Sulkava, V. Ala-Hurula, M. Poyhonen, B. Frangione, H. Houlden, R. Crook, A. Goate, S. Pandit, H. Donis-Keller, L. Liu, K. Axelman, L. Forsell, L. Lannfelt, and J. Hardy (1994). Chromosome 14 – encoded Alzheimer’s Disease: Genetic and Clinicopathological Description. Annals of Neurology, 36: 362-367.
  • Garver, R. I., Jr., D. M. Radford, H. Donis-Keller, M. R. Wick, and P. G. Milner (1994). Midkine and pleiotropin expression in normal and malignant breast tissue. Cancer, 74: 1584-1590.
  • Kaufman, B. A., P. S. White, T. Steinbrueck, H. Donis-Keller, and G. M. Brodeur (1994). Linkage mapping of the TNFR2 gene to 1p36.2 using the SSCP technique. Human Genetics, 94 (4): 418-422.
  • Kobayashi, H., K. T. Montgomery, S. K. Bolhlander, C. N. Adra, B. L. Lim, R. S. Kucherlapati, H. Donis-Keller, M. S. Holt, M. M. LeBeau, and J. D. Rowley (1994). Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases. Blood, 84: 3773-3482.
  • Tanizawa, Y., A. C. Riggs, S. Dagogo-Jack, M. Vaxillaire, P. Froguel, L. Liu, H. Donis-Keller, and M. A. Permutt. (1994). Isolation of the human LIM/homeodomain gene Islet-1 (Isl-1) and identification of a simple sequence repeat polymorphism. Diabetes, 43: 935-941.
  • Glaser, B., R. Anker, K. C. Chiu, H. Donis-Keller, and M. A. Permutt (1994). Dinucleotide repeat polymorphism at the human gastrin/cholecystokinin type B receptor (CCKBR) locus on 11p15.4. Human Molecular Genetics, 3(11): 2081.
  • Lairmore, T. C., S. Dou, J. R. Howe, D. Chi, K. Carlson, R. Veile, S. K. Mishra, S. A. Wells, Jr., and H. Donis-Keller (1993). A 1.5 megabase contig of yeast artificial chromosome clones containing three loci (RET, D10S94, and D10S102) closely linked to the MEN2A locus. Proceedings of the National Academy of Science, USA 90: 492-496.
  • Howe, J. R., T. C. Lairmore, R. Veile, S. Dou, S. A. Wells, Jr., and H. Donis-Keller (1993). Development of a sequence-tagged site for the centromere of chromosome 10: its use in cytogenetic and physical mapping. Human Genetics, 91: 199-204.
  • Crouch, E., K. Rust, R. Veile, H. Donis-Keller, and L. Grosso (1993). Genomic Organization of human surfactant protein D: SP-D is encoded on chromosome 10q22.2-23.1. Journal of Biological Chemistry, 268: 2976-2983.
  • York, J. D., R. A. Veile, H. Donis-Keller, and P. W. Majerus (1993). The cloning, heterologous expression and chromosomal localization of human inositol polyphosphate 1-phosphatase. Proceedings of the National Academy of Science, USA, 90: 5833-5837.
  • Radford, D. M., K. Fair, A. M. Thompson, T. Steinbrueck, M. Holt, J. H. Ritter, M. Wallace, D. Patterson, S. A. Wells, Jr., and H. Donis-Keller (1993). Allelic loss on chromosome 17 in ductal carcinoma in situ of the breast. Cancer Research, 53: 2947-2950.
  • Lengauer, C., M. R. Speicher, S. Popp, A. Jauch, M. Taniwaki, R. Nagaraja, H. Riethman, H. Donis-Keller, M. D’Urso, D. Schlessinger, and T. Cremer (1993). Chromosomal bar codes produced by multicolor fluorescence in situ hybridization with multiple YAC clones and whole chromosome painting probes. Human Molecular Genetics, 2: 505-512.
  • Ball, D. W., C. G. Azzoli, S. B. Baylin, D. Chi, S. Dou, H. Donis-Keller, A. Cumaraswamy, M. Borges, and B. D. Nelkin (1993). Identification of a human achaete-scute homolog highly expressed in neuroendocrine tumors. Proceedings of the National Academy of Science, USA , 90: 5648-5652.
  • Hing, A. V., C. Helms, and H. Donis-Keller (1993). VNTR and microsatellite polymorphisms within the subtelomere region of 7q. American Journal of Human Genetics, 53: 509-517.
  • Donis-Keller, H. S. Dou, D. Chi, Katrin M. Carlson, K. Toshima, T. C. Lairmore, J. R. Howe, J. F. Moley, P. F. Goodfellow, and S. A. Wells, Jr. (1993). Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Human Molecular Genetics, 2: 851-856.
  • Litt, M., P. Kramer, X. Y. Hauge, J. L. Weber, Z. Wang, P. J. Wilkie, M. S. Holt, S. Mishra, H. Donis-Keller, L. Warnich, A. E. Retief, C. Jones, and J. Weissenbach (1993). A microsatellite-based index map of human chromosome 11. Human Molecular Genetics, 2: 909-913.
  • Hing, A. V., J. Corteville, R. P. Foglia, H. Donis-Keller, and S. B. Dowton (1993). Fetus in Fetu: Molecular analysis of a fetiform mass. American Journal of Medical Genetics, 47: 333-341.
  • Radford, D. M., K. L. Fair, A. M. Thompson, J. H. Ritter, M. Holt, S. A. Wells, Jr., and H. Donis-Keller (1993). Chromosomal regions implicated in the development of breast cancer. Surgical Forum, 44: 502-504.
  • Wood, S., K. B. Othmane, U. S. R. Bergerheim, S. H. Blanton, R. Bookstein, R. A. Clarke, S. P. Daiger, H. Donis-Keller, D. Drayna, S. Kumar, R. J. Leach, H-J. Ludecke, J. Oshima, L. A. Sadler, N. K. Spurr, T. Steinbrueck, J. Trapman, M. Wagner, Z. Wang, D. Wells, and C. A. Westbrook (1993). Report of the first international workshop on human chromosome 8 mapping. Cytogenetics and Cell Genetics, 64: 134-146.
  • Popp, S., A. Jauch, D, Schindler, M. R. Speicher, C. Lengauer, H. Donis-Keller, H. C. Reithman, and T. Cremer (1993). A strategy for the characterization of minute chromosome rearrangements using multicolor fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones. Human Genetics, 92:527-532.
  • Matsutani, A., R. Janssen, H. Donis-Keller, and M. A. Permutt (1992). A polymorphic (CA)n repeat element maps the human glucokinase GCK (E.C. 2.7.1.2) gene to chromosome 7p. Genomics, 12: 319-325.
  • Mishra, S. K., C. Helms, D. Dorsey, M. A. Permutt, and H. Donis-Keller (1992). A 2 cM genetic linkage map of human chromosome 7p that includes 47 loci. Genomics, 12: 326-334.
  • Crosby, S. D., R. Veile, H. Donis-Keller, J. M. Baraban, K. Simburger, M. A. Watson, and J. Milbrandt (1992). Neural specific expression and genomic structure of transcription factor NGFI-C. Proceedings of the National Academy of Science, USA, 89: 4739-4743.
  • Howe, J. R., T. C. Lairmore, S. Dou, R. Veile, T. Steinbrueck, S. A. Wells Jr., and H. Donis-Keller (1992 ). A new RFLP marker D5S348 maps to 5p14.3-15.2, between D5S60 (CRI-R535) and HPRTP2. Nucleic Acids Research, 20: 1168.
  • Iwasaki, H., P. W. Stewart, W. G. Dilley, M. S. Holt, S. A. Wells, Jr., and H. Donis-Keller (1992). A minisatellite and a microsatellite polymorphism within 1.5 kb at the human muscle glycogen phosphorylase (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95. Genomics, 13: 7-13.
  • Anker, R., T. Steinbrueck, and H. Donis-Keller (1992). Tetranucleotide repeat polymorphism at the human thyroid peroxidase (hTPO) locus. Human Molecular Genetics, 1: 137.
  • Chi, D. D., A. V. Hing, C. Helms, C., T. Steinbrueck, S. K. Mishra, and H. Donis-Keller (1992). Two chromosome 7 dinucleotide repeat polymorphisms at gene loci Epidermal Growth Factor Receptor (EGFR) andProa2 (I) Collagen locus (COL1A2). Human Molecular Genetics, 1: 135.
  • Warlick, C. A., S. Ramachandra, S. K. Mishra, and H. Donis-Keller (1992). Dinucleotide repeat polymorphism at the human cardiac b-myosin heavy chain gene (HMSYHCO1) locus. Human Molecular Genetics, 1: 136.
  • Weaver, R., C. Helms, S. K. Mishra, and H. Donis-Keller (1992). Software for analysis and manipulation of genetic linkage data. American Journal of Human Genetics, 50: 1267-1274.
  • Drury, H. A., K. W. Clark, R. Hermes, J. M. Feser, L. Thomas, Jr., and H. Donis-Keller (1992). A graphical user interface for quantitative imaging and analysis of electrophoretic gels and autoradiograms. BioTechniques, 12: 892-898.
  • Matsutani, A., A. V. Hing, T. Steinbrueck, R. Janssen, J. Weber, A. M. Permutt, and H.
  • Donis-Keller (1992). Mapping the human liver/islet glucose transporter (GLUT-2) gene within a genetic linkage map of chromosome 3q using a (CA)n dinucleotide repeat polymorphism and characterization of the polymorphism in 3 racial groups. Genomics, 13: 495-501.
  • Howe, J. R., T. C. Lairmore, S. Dou, S. K. Mishra, W. G. Dilley, H. Donis-Keller, and S. A. Wells, Jr. (1992). Presymptomatic identification of carriers of the MEN2A gene using flanking DNA markers. Surgery, 112: 219-226.
  • NIH/CEPH Collaborators Mapping Group (1992). A comprehensive genetic linkage map of the human genome. Coordinating editor and senior authorship for maps of chromosomes 2, 6, 7, 8, 12, 14. Science, 258: 67-86 and 148-162.
  • Freije, D., C. Helms, M. S. Watson, and H. Donis-Keller (1992). Identification of a second pseudoautosomal region near the Xq and Yq telomeres. Science, 258:1784-1787.
  • Howe, J. R., T. C. Lairmore, S. K. Mishra, S. Dou, R. Veile, S. A. Wells, Jr., and H. Donis-Keller (1992). Improved predictive test for MEN2 using flanking dinucleotide repeats and RFLPs. American Journal of Human Genetics, 51: 1430-1442.
  • Clark, A.J., and H. Donis-Keller (1992). Mammalian gene studies editorial overview. Current Biolgy, 3: 595-596.
  • Milner, P., D. Shah, R. Veile, H. Donis-Keller, and B. V. Kumar (1992). Cloning, nucleotide sequence and chromosome localization of the human pleiotropin (PTN) gene. Biochemistry, 31: 12023-12028.
  • Helms, C., S. K. Mishra, H. Riethman, A.K. Burgess, S. Ramachandra, C. Tierney, D. Dorsey, and H. Donis-Keller (1992). Closure of a 2.4 cM genetic linkage map of human chromosome 7q with centromere and telomere polymorphisms. Genomics, 14: 1041-1054.
  • Spurr, N. K., S. Cox, S. P. Bryant, J. Attwood, E. A. Robson, D. Shields, T. Steinbrueck, T., Jenkins, J. C. Murray, K. K. Kidd, J. Philips, P. Tsipouras, A. E. Reitef, T. A. Kruse, A. E. Bale, G. Vergnaud, J. Weber, O. W. McBride, H. Donis-Keller, and R. L. White (1992). CEPH consortium linkage map of human chromosome 2. Genomics, 14: 1055-1063.
  • Lairmore, T. C., J. R. Howe, S. Dou, R. Veile, J. A. Korte-Sarfaty, S. A. Wells, Jr. and H. Donis-Keller (1992). Isolation of YAC clones from the pericentromeric region of chromosome 10 and development of new genetic markers linked to the multiple endocrine neoplasia type 2A . (1992) Henry Ford Hospital Medical Journal, 40: 210-214.
  • Lairmore, T. C., J. R. Howe, S. Dou, D. Chi, K. Carlson, S. K. Mishra, S. A. Wells, Jr., and H. Donis-Keller (1992). Presymptomatic genetic testing for familial medullary thyroid carcinoma. Surgery XLIII: 462-464.
  • Mishra, S.K., C. Helms, D. Dorsey, M.A. Permutt, and H. Donis-Keller (1992). A 2-cM genetic linkage map of human chromosome 7p that includes 47 loci. Genomics, 12(2): 326-334.
  • Lairmore, T. C., J. R. Howe, J. A. Korte, W. G. Dilley, L. Aine, E. Aine, S. A. Wells Jr. and H. Donis-Keller (1991). Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A. Genomics, 9: 181-192.
  • Dracopoli, N. C., P. O’Connell, T.I. Elsner, J-M. Lalouel, R.L. White, K.H. Buetow, D.Y. Nishimura, J. C. Murray, C. Helms, S. K. Mishra, H. Donis-Keller, J. M. Hall, M. K. Lee, M-C. King, J. Attwood, N. E. Morton, E. B. Robson, M. Mahtani, H. F. Willard, N. J. Royle, I. Patel, A. J. Jeffreys, V. Verga, J. L. Weber, A. L. Mitchell, and A. Bale (1991). The CEPH consortium linkage map of human chromosome 1. Genomics, 9: 686-700.
  • Weiffenbach, B., K. Falls, A. Bricker, L Hall, J. McMahon, J. Wasmuth, V. Funanage and H. Donis-Keller (1991). A genetic linkage map of human chromosome 5 with 60 RFLP Loci. Genomics, 10: 173-185.
  • Lairmore, T. C., A. Vocero Villeta, S. Dou, T. Steinbrueck and H. Donis-Keller (1991). A new RFLP locus D4S185 maps to human chromosome 4q. Nucleic Acids Research, 19: 2518.
  • Howe, J. R., J. A. Korte, S. Dou, T. Steinbrueck and H. Donis-Keller (1991). A new RFLP marker D12S54 maps between F8VWF and KRAS2 on human chromosome 12p. Nucleic Acids Research, 19: 2512.
  • Kere, J., R. Tolvanen, H. Donis-Keller, and A. de la Chapelle (1991). Refinement of human chromosome 7 map around the proalpha2(I) collagen gene by long-range restriction mapping. Nucleic Acids Research 19: 2755-2759.
  • Farrer, L. A., A. M. Bowcock, J. M. Hebert, B. Bonne-Tamir, I. Sternlieb, M. Giagheddu, P. St. George-Hyslop, M. Frydman, J. Lobner, L. Demelia, C. Carcassi, R. Lee, R. Bekker, A. E. Bale, H. Donis-Keller, I. H. Scheinberg and L. L. Cavalli-Sforza (1991). Predictive testing for Wilson disease using tightly linked and flanking DNA markers. Neurology, 41: 992-999.
  • Howe, J. R., T. C. Lairmore, S. Dou, J. A. Korte, S. A. Wells, Jr., and H. Donis-Keller (1991). Confirmation of genetic homogeneity in multiple endocrine neoplasia type 2A. Surgical Forum, 42: 432-435.
  • Clark, A. J. and H. Donis-Keller (1991). Mammalian gene studies editorial overview. Current Biology, 2: 785-786.
  • Keith, T. P., P. Green, S. T. Reeders, V. A. Brown, P. Phipps, A. Bricker, K. Falls, K. Rediker, J. A. Powers, C. Hogan, C. Nelson, R. Knowlton and H. Donis-Keller (1990). Genetic linkage map of 45 DNA markers on human chromosome 16. Proceedings of the National Academy of Science, USA. 87: 5754-5758.
  • White, R., J.-M. Lalouel, Y. Nakamura, H. Donis-Keller, P. Green, D. Bowden, C. Matthew, D.Easton, E. Robson, N. Morton, J. Gusella, J. Haines, A. Retief, K. Kidd, J. Murray, M. Lathrop and H. Cann (1990). The CEPH consortium primary linkage map of human chromosome 10. Genomics, 6: 393-412.
  • Stephens, K., P. Green, V. M. Riccardi, S. Ng, M. Rsing, D. Barker, J. K. Darby, K. Falls, F. Collins, H. F. Willard and H. Donis-Keller. (1989). Genetic analysis of eight loci tightly linked to neurofibromatosis 1. American Journal of Human Genetics, 44: 13-19.
  • Knowlton, R. G., C. A. Nelson, V. A. Brown, D. C. Page and H. Donis-Keller (1989). An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome. Nucleic Acids Research, 17: 423-437.
  • Fulton, T. R., A. M. Bowcock, D. R. Smith, L. Daneshvar, P. Green, L. Cavalli-Sforza and H. Donis-Keller (1989). A 12 megabase restriction map at the cystic fibrosis locus. Nucleic Acids Research, 17: 271-284.
  • Bale, S. J., N. C. Dracopoli, M. A. Tucker, W. H. Clark Jr., M. C. Fraser, P. Green, H. Donis-Keller, M. H. Greene and D. E. Houseman (1989). Hereditary cutaneous malignant melanoma maps to the short arm of chromosome 1. New England Journal of Medicine, 320(May 25): 1367-1372.
  • Bowden, D. W., H. Muller-Kahle, T. C. Gravius, C. Helms, D. Watt-Morgan, P. Green, and H. Donis-Keller (1989). Identification and characterization of 23 restriction fragment length polymorphic loci by screening random cosmid genomic clones. American Journal of Human Genetics, 44: 671-678.
  • Green, P., C. Helms, B. Weiffenbach, K. Stephens, T. Keith, D. Bowden, D. Smith, and H. Donis-Keller (1989). Construction of a linkage map of the human genome, and its application to mapping genetic diseases. Clinical Chemistry, 35(7) Suppl. B: B33-B37.
  • Smith, D.R., D.T.R. Fulton, P. Swain, A. Bowcock, L. Daneshvar, C. Traver, D.C. Gruenert, R. Davis, L.L. Cavalli-Sforza, and H. Donis-Keller (1989). Cystic fibrosis: diagnostic testing and the search for the gene. Clinical Chemistry, 35(7) Suppl.B: B17-B20.
  • Cohen-Haguenauer, O., N. Van Cong, R. Knowlton, M.-F. deTand, C. Jegou, M.-S. Gross, V. A. Brown, J. Frezal and H. Donis-Keller (1989). Chromosomal assignment of 14 genomic probes for highly polymorphic loci. Cytogenetics and Cell Genetics, 50: 78-83.
  • Bowden, D. W., T. C. Gravius, P. Green, K. Falls, D. Wurster-Hill, W. Noll, H. Muller-Kahle and H. Donis-Keller (1989). A genetic linkage map of 32 loci on human chromosome 10. Genomics, 5: 718-726.
  • Jarcho, J. A., W. McKenna, J. A. Peter Pare, S. D. Solomon, R. F. Holcombe, S. Dickie, L. Tatjana, H. Donis-Keller, J. G. Seidman and C. Seidman (1989). Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1. New England Journal of Medicine, 321: 1372-1378.
  • Kere, J., H. Donis-Keller, T. Ruutu, and A. de la Chapelle (1989). Chromosome 7 long arm deletions in myeloid disorders: terminal DNA sequences are commonly conserved and breakpoints vary. Cytogenetics and Cell Genetics, 50: 226-229.
  • Nugent, C. E., T. Gravius, P. Green, J. W. Larsen, M. D. McMillin and H. Donis-Keller (1988). Prenatal diagnosis of cystic fibrosis by chorionic villus sampling using 12 polymorphic DNA markers. Journal of Obstetrics and Gynocology, 71: 213-215.
  • Schumm, J. W., R. G. Knowlton, J. C. Braman, D. Barker, D. Botstein, B. Akots, V. Brown, T. Gravius, C. Helms, K. Hsaio, K. Rediker, J. Thurston and H. Donis-Keller (1988). Detection of more than 500 single copy RFLPs by random screening. American Journal of Human Genetics ,42: 143-159.
  • Bowden, D. W., H. Muller-Kahle, T. R. Fulton, T. C. Gravius, D. R. Barker and H. Donis-Keller (1988). Studies on locus expansion, library representation, and chromosome walking using an efficient method to screen cosmid libraries. Gene, 71: 391-400.
  • Kazazian, H. H. Jr., S. H. Orkin, C. D. Boehm, S. C. Goff, C. Wong, C. E. Dowling, P. E. Newberger, R. G. Knowlton, V. A. Brown and H. Donis-Keller (1986). Characterization of a spontaneous mutation to a B-thalassemia allele. American Journal of Human Genetics, 38: 860-867.
  • Yam, P. Y., L. D. Petz, R. G. Knowlton, R. B. Wallace, A. D. Stock, G. deLange, V. A. Brown, H. Donis-Keller and K. G. Blume (1987). Use of DNA restriction fragment length polymorphisms to document marrow engraftment and mixed hematopoietic chimerism following bone marrow transplantation. Transplantation, 43: 399-407.
  • Donis-Keller, H., P. Green, C. Helms, S. Cartinhour, B. Weiffenbach, K. Stephens, T. P. Keith, D. W. Bowden, D. R. Smith, E. S. Lander, D. Botstein, G. Akots, K. S. Rediker, T. Gravius, V. A. Brown, M. B. Rising, C. Parker, J. A. Powers, D. E. Watt, E. R. Kauffman, A. Bricker, P. Phipps, H. Muller-Kahle, T. R. Fulton, S. Ng, J. W. Schumm, J. C. Braman, R. G. Knowlton, D. F. Barker, S. M. Crooks, S. E. Lincoln, M. J. Daly and J. Abrahamson. (1987). A genetic linkage map of the human genome. Cell, 51(October 23): 319-337.
  • Barker, D., P. Green, R. Knowlton, J. Schumm, E. Lander, A. Oliphant, H. Willard, G. Akots, V. Brown, T. Gravius, C. Helms, C. Nelson, C. Parker, K. Rediker, M. Rising, D. Watt, B. Weiffenbach and H. Donis-Keller (1987). Genetic linkage map of human chromosome 7 with 63 DNA markers. Proceedings of the National Academy of Science, USA, 84 (November): 8006-8010.
  • Stephens, K., V. M. Riccardi, M. Rising, S. Ng, P. Green, F. S. Collins, K. S. Rediker, J. A. Powers, C. Parker and H. Donis-Keller (1987). Linkage studies with chromosome 17 DNA markers in 45 neurofibromatosis-1 families. Genomics, 1: 353-357.
  • L.D. Petz, P.Y. Yam, R.B. Wallace, A. D. Stock, G. de Lang, R.G. Knowlton, V.A. Brown, H. donis-Keller, L.R. Hill, S.J. Forman, and K.G. Blume (1986). Mixed hematopoetic chimerism following bone marrow transplantation for hematologic malignancies. Blood, 70(5): 1331-1337.
  • Buchwald, M., H. Willard, M. Schwartz, K. Schmigelo, D. Kennedy, N. Plavsic, M. Zsiga, S. Sengerling, D. Barker, H. Donis-Keller and L.-C. Tsui (1986). Linkage of cystic fibrosis to pro alpha-2 collagen gene, COL1A2 on chromosome 7. Cytogenetics and Cell Genetics, 41: 234-239.
  • Knowlton, R. G., V. A. Brown, J. C. Braman, D. Barker, J. W. Schumm, C. Murray, T. Takvorian, J. Ritz and H. Donis-Keller (1986). Use of highly polymorphic DNA probes for genotypic analysis following bone marrow transplantation. Blood, 68(2): 378-385.
  • Tsui, L.C., M. Buchwald, D. Barker, J. C. Braman, R. G. Knowlton, J. W. Schumm, H. Eiberg, J. Mohr, D. Kennedy, N. Plavsic, M. Zsiga, D. Markiewicz, G. Akots, V. Brown, C. Helms, T. Gravius, C. Parker, K. Rediker and H. Donis-Keller (1985). Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker. Science, 230: 1054-1057.
  • Knowlton, R. G., O. Cohen-Haguenauer, N. Van Cong, J. Frezal, V. A. Brown, D. Barker, J. C. Braman, J. W. Schumm, L.-C. Tsui, M. Buchwald and H. Donis-Keller (1985). A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7. Nature, 318: 380-382.
  • Reed, R. E., M. F. Baer, C. Guerrier-Takada, H. Donis-Keller and S. Altman (1982). Nucleotide sequence of the gene encoding the RNA subunit (M1 RNA) of ribonuclease P from Escherichia coli. Cell, 30: 627-636.
  • Donis-Keller, H., K. Browning and J. M. Clark Jr. (1981). Sequence heterogeneity in satellite tobacco necrosis virus RNA. Virology, 110: 43-54.
  • Donis-Keller, H. (1980). Phy M: an RNase activity specific for U and A residues useful in RNA sequence analysis.” Nucleic Acids Research, 8: 3133-3142.
  • Donis-Keller, H., J. Rommelaere, R. W. Ellis and N. Hopkins (1980). Nucleotide sequences associated with difference in electrophoretic mobility of envelope glycoprotein gp70 and with G9 antigen phenotype of certain murine leukemia viruses. Proceedings of the National Academy of Science, USA, 77: 1642-1645.
  • Rommelaere, J., H. Donis-Keller and N. Hopkins (1979). RNA sequencing provides evidence for allelism of determinants of the N-, B-, or NB- tropism of murine leukemia viruses. Cell, 16: 43-50.
  • Donis-Keller, H. (1979). Site specific enzymatic cleavage of RNA. Nucleic Acids Research, 7: 179-192.
  • Donis-Keller, H., A. Maxam and W. Gilbert (1977). Mapping adenines, guanines, and pyrimidines in RNA. Nucleic Acids Research, 4: 2527-2538.
  • Efstratiadis, A., J. N. Vournakis, H. Donis-Keller, B. Chaconas, D. K. Dougall and F. Kafatos (1977). End labelling of enzymatically decapped mRNA. Nucleic Acids Research, 4: 4165-4174.

Electronic (Computer Programs)

  • Weaver, R., C. Helms, S. K. Mishra, and H. Donis-Keller (1992). Software for analysis and manipulation of genetic linkage data. American Journal of Human Genetics, 50: 1267-1274.
  • Drury, H. A., K. W. Clark, R. Hermes, J. M. Feser, L. Thomas, Jr., and H. Donis-Keller (1992). A graphical user interface for quantitative imaging and analysis of electrophoretic gels and autoradiograms. BioTechniques, 12: 892-898.

Book Chapters or Sections in Books

  • Pandit, S. D., and H. Donis-Keller (1996). Human chromosome 14 genetic and physical map status. Encyclopedia of Molecular Biology, VCH Publishers, N.Y., pp.142 – 160.
  • NIH/CEPH Collaborators Mapping Group (1993). A Comprehensive Genetic Linkage Map of the Human Genome Genetic Maps. Sixth Edition, Book 5: Human Maps pgs. 5.82-5.105. New York, Cold Spring Harbor Press.
  • Donis-Keller, H. (1992). The Commercial Aspect of Diagnostic Testing. in Fundacion BBV Documenta Human Genome Project: Ethics. Foundation BBV Madrid. 323-331.
  • Donis-Keller, H. and V. Buckle (1991). Report of the committee on the genetic constitution of chromosome 8. Cytogenetics and Cell Genetics. Basel, Karger. 58: 382-402.
  • Donis-Keller, H. and V. Buckle (1990). Report of the committee on the genetic constitution of chromosome 8. Cytogenetics and Cell Genetics. Basel, Karger. 55:128-135.
  • Donis-Keller, H. and C. Helms (1990). An on average 6 cM RFLP linkage map of the human genome. Genetic Maps. Fifth Edition, Book 5: Human Maps pgs. 5.158-1.182. New York, Cold Spring Harbor Press.
  • Donis-Keller, H. (1989). Disease diagnosis using restriction fragment length polymorphisms. Genetic Engineering Technology in Industrial Pharmacy. New York, Marcel Dekker.
  • Tsui, L.-C., M. Farrall, and H. Donis-Keller (1989). Report of the committee on the genetic constitution of chromosomes 7 and 8. Cytogenetics and Cell Genetics. Human Gene Mapping 10. Basel, Karger. pgs166-201.
  • Donis-Keller, H. and D. Botstein (1988). Recombinant DNA methods: applications to human genetics. Progress in Medical Genetics. New York, Elsevier Science Publishing Co.
  • Tsui, L.-C., M. Farrall, and H. Donis-Keller (1988). Report of the committee on the genetic constitution of chromosomes 7 and 8. Cytogenetics and Cell Genetics. Human Gene Mapping 9.5. Basel, Karger.
  • Green, P., D. Barker, R. Knowlton, J. Schumm, E. Lander, A. Oliphant, H. Willard, G. Akots, V. Brown, T. Gravius, C. Helms, C. Nelson, C. Parker, K. Rediker, M. Rising, D. Watt, B. Weiffenbach and H. Donis-Keller (1987). A genetic linkage map of chromosome 7 including the cystic fibrosis region. Cellular and Molecular Basis of Cystic Fibrosis. San Franscisco, San Franscisco Press.
  • Donis-Keller, H., D. Barker, R. G. Knowlton, J. Schumm and J. Braman (1986). Applications of RFLP probes to genetic mapping and clinical diagnosis in humans. Applications of DNA Probes: Banbury Report. Cold Spring Harbor, Cold Spring Harbor Press.
  • Donis-Keller, H., D. F. Barker, R. G. Knowlton, J. W. Schumm, J. C. Braman, and P. Green (1986). Highly polymorphic RFLP probes as diagnostic tools. The Cold Spring Harbor Symposium: The Molecular Biology of Homo Sapiens. Cold Spring Harbor, Cold Spring Harbor Press.
  • Knowlton, R., V. Brown, J. Braman, D. Barker, J. Schumm, J. Ritz and H. Donis-Keller (1986). Genotypic analysis of cell populations with highly polymorphic DNA probes. Recent Advances in Bone Marrow Transplantation. New York, Alan R. Liss, Inc.
  • Petz, L. D., P. Yam, R. B. Wallace, A. D. Stock, G. deLange, R. G. Knowlton, V. A. Brown, H. Donis-Keller, and K. G. Blume. (1986). Mixed hematopoietic chimerism following bone marrow transplantation for hematologic malignancies: incidence, characterization, and implications for GVHD and leukemic relapse. Recent Advances in Bone Marrow Transplantation. New York, Alan R. Liss, Inc.
  • Botstein, D. and H. Donis-Keller. (1984). A molecular approach to defining the inherited components in epilepsy and other diseases of uncertain etiology. Epilepsia. New York, Raven Press.
  • Fields, B. N., H. L. Weiner, D. T. Drayna, A. H. Sharpe, D. Hardy, D. Rubin, S. Burstin, R. Ahmed, J. Gentsch, and H. Donis-Keller. (1980). The molecular basis of reovirus virulence. Animal Virus Genetics. New York, Academic Press, Inc.

Books

  • Donis-Keller, H., Crossing the Portal: Enduring Doorways, in preparation, 2014
  • Donis-Keller, H., Iceland and Death Valley: Extreme Environments at Tectonic Plate Boundaries, A Portfolio of Photographs, Published and available from Blurb.com, 2012
  • Donis-Keller, H., Lost: Cherished Companions Who Have Gone Astray, eBook, Published and available from Blurb.com, 2012, eBook also available from the Apple iBookstore and Blurb.com
  • L. Poissant and Daubner, E. Art et Biotechnologies, Presses de l’Universite du Quebec, 2005. ISBN 2-7605-1328-9, 390 pages. Artworks by H. Donis-Keller are included in a CD ROM anthology of artworks that are a part of this book of essays. See also www.gram-arts.org
  • Andrews, L. B., Fullarton, J. E., Hanna, K. E., Holtman, N. A. and A. G. Motulsky, Eds. Assessing Genetic Risk: Implications for Health and Social Policy, Committee on Assessing Genetic Risks, Division of Health Sciences Policy, Institute of Medicine, National Academy Press, 1994. (member of Committee, wrote minor sections, participated in editing and review of manuscript).