Skip to Main Content

Author Details

Misha Angrist
Duke University.
1989
47
18
PMIDPaper TitleJournal TitlePublished Year
34704909Stop the Madness: Dementia, "Radical Medicalization," and Straw Men.AJOB Neurosci2021
33095048Reactions to the National Academies/Royal Society Report on <i>Heritable Human Genome Editing</i>.CRISPR J2020
33043412Good problems to have? Policy and societal implications of a disease-modifying therapy for presymptomatic late-onset Alzheimer's disease.Life Sci Soc Policy2020
33052113Participant-Partners in Genetic Research: An Exome Study with Families of Children with Unexplained Medical Conditions.J Particip Med2018
27047752Personal genomics: Where are we now?Appl Transl Genom2016
25045831Living laboratory: whole-genome sequencing as a learning healthcare enterprise.Clin Genet2015
26184591Start me up: ways to encourage sharing of genomic information with research participants.Nat Rev Genet2015
23656395Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes SEDT.Clin Genet2014
25621201The audacity of interpretation: Protecting patients or piling on?Appl Transl Genom2014
25642409Distributing the future: The weak justifications for keeping human genomic databases secret and the challenges and opportunities in reverse engineering them.Appl Transl Genom2014
25059740Personalized medicine and human genetic diversity.Cold Spring Harb Perspect Med2014
24647311Open window: when easily identifiable genomes and traits are in the public domain.PLoS One2014
23389508Genetic privacy needs a more nuanced approach.Nature2013
22797899A public resource facilitating clinical use of genomes.Proc Natl Acad Sci U S A2012
22199990You never call, you never write: why return of 'omic' results to research participants is both a good idea and a moral imperative.Per Med2011
20373666Personal genomes in progress: from the human genome project to the personal genome project.Dialogues Clin Neurosci2010
20818549Urge overkill: protecting deidentified human subjects at what price?Am J Bioeth2010
20697400DNA patents and diagnostics: not a pretty picture.Nat Biotechnol2010
20393304Impact of gene patents and licensing practices on access to genetic testing for long QT syndrome.Genet Med2010
20359249Only connect: personal genomics and the future of American medicine.Mol Diagn Ther2010
19325608The dangers of diagnostic monopolies.Nature2009
22328898Eyes wide open: the personal genome project, citizen science and veracity in informed consent.Per Med2009
19998110We are the genes we've been waiting for: rational responses to the gathering storm of personal genomics.Am J Bioeth2009
16789312Who owns the genome?New Atlantis2006
29793285The future may be closer than you think: a response from the Personalized Medicine Coalition to the Royal Society's report on personalized medicine.Per Med2006
17023637Public health. Genomics and medicine at a crossroads in Chernobyl.Science2006
15629848Breast cancer: integrating the patient with her genome.Trends Biotechnol2005
16096102Genomic medicine: genetic variation and its impact on the future of health care.Philos Trans R Soc Lond B Biol Sci2005
11891057Cloning of rat thymic stromal lymphopoietin receptor (TSLPR) and characterization of genomic structure of murine Tslpr gene.Gene2002
11953745Segregation at three loci explains familial and population risk in Hirschsprung disease.Nat Genet2002
10618407A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.Proc Natl Acad Sci U S A2000
10077527The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome.Genome Res1999
9685314Less is more: compact genomes pay dividends.Genome Res1998
9881709Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease.Oncogene1998
10072588Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome 19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR.Cytogenet Cell Genet1998
9545641Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility.Genomics1998
9068584Does phaster mean better?Clin Chem1997
8630503A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome).Nat Genet1996
8896568Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.Nat Genet1996
8826440Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.Am J Med Genet1996
8696331Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome.Nat Genet1996
7633441Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.Hum Mol Genet1995
8825655Chromosomal localization of the mouse Src-like adapter protein (Slap) gene and its putative human homolog SLA.Genomics1995
7849714Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.Hum Mol Genet1994
7987295Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22.Hum Mol Genet1994
8401581A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.Nat Genet1993
2708299Autism resources at the higher education level in Indiana.J Autism Dev Disord1989
  • 1 - 47 of 47

Recommended Authors

Edmond & Lily Safra Center for Ethics, Harvard University
Career Start Year 2009
Number of shared co-authors 0
Hospital for Sick Children, Canada University of Toronto
Career Start Year 2008
Number of shared co-authors 0
Vagelos College of Physicians and Surgeons, Columbia University
Career Start Year 2007
Number of shared co-authors 4
University of Maryland School of Medicine
Career Start Year 2006
Number of shared co-authors 0
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 4
Invitae Corporation
Career Start Year 2004
Number of shared co-authors 3
University of Toronto.
Career Start Year 2003
Number of shared co-authors 1
McGill University.
Career Start Year 2003
Number of shared co-authors 6
University of Exeter, Royal Devon and Exeter Hospital
Career Start Year 2003
Number of shared co-authors 2
Baylor College of Medicine.
Career Start Year 2002
Number of shared co-authors 16
Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
Career Start Year 2002
Number of shared co-authors 4
Reichman University (IDC) Herzliya
Career Start Year 2001
Number of shared co-authors 0
Stanford Center for Biomedical Ethics (SCBE), Stanford University
Career Start Year 2000
Number of shared co-authors 9
University of North Carolina
Career Start Year 1999
Number of shared co-authors 4
University of Washington School of Medicine
Career Start Year 1994
Number of shared co-authors 9
Dartmouth Geisel School of Medicine
Career Start Year 1993
Number of shared co-authors 5
Clinical Ethics, University of Oxford
Career Start Year 1992
Number of shared co-authors 2
Genomic Medicine Institute
Career Start Year 1991
Number of shared co-authors 6
University of Wisconsin School of Law, Morgridge Institute for Research.
Career Start Year 1991
Number of shared co-authors 3
University of North Carolina
Career Start Year 1989
Number of shared co-authors 6
Kaiser Permanente Washington
Career Start Year 1987
Number of shared co-authors 2
National Human Genome Research Institute, National Institutes of Health
Career Start Year 1987
Number of shared co-authors 12
Harvard Medical School
Career Start Year 1985
Number of shared co-authors 7
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Career Start Year 1985
Number of shared co-authors 12
Center for Biomedical Ethics, Stanford University School of Medicine
Career Start Year 1985
Number of shared co-authors 10
University of Washington Medical Center
Career Start Year 1985
Number of shared co-authors 8
Centers for Disease Control and Prevention Atlanta GA USA.
Career Start Year 1981
Number of shared co-authors 6
University of Michigan ann arbor
Career Start Year 1978
Number of shared co-authors 13
McGill University
Career Start Year 1978
Number of shared co-authors 14
The Heart Institute, Cincinnati Children's Hospital Medical Center
Career Start Year 1975
Number of shared co-authors 11

Collaborators

New York University Grossman School of Medicine
Co-authored papers 13
Arizona State University.
Co-authored papers 8
Harvard Medical School
Co-authored papers 3
Co-authored papers 3
Co-authored papers 3
National Institutes of Health
Co-authored papers 3
National Institutes of Health
Co-authored papers 3
Wyss Institute for Biologically Inspired Engineering, Harvard University
Co-authored papers 3
Northwestern University
Co-authored papers 2
Harvard Medical School
Co-authored papers 2
Co-authored papers 2
Northwestern University Feinberg School of Medicine
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Stanford University
Co-authored papers 1
GenOmics and Translational Research Center
Co-authored papers 1
Yale School of Medicine
Co-authored papers 1
College of Health and Medicine, The Australian National University
Co-authored papers 1
National Centre for Biotechnology (CNB-CSIC)
Co-authored papers 1
Neaman Center for Personalized Medicine, NorthShore University HealthSystem
Co-authored papers 1
Dalla Lana School of Public Health, University of Toronto
Co-authored papers 1
Universidade Federal de Sao Paulo
Co-authored papers 1
American University of Beirut Medical Center
Co-authored papers 1
Broad Institute of MIT and Harvard
Co-authored papers 1
Department of Food and Nutrition, Kongju National University
Co-authored papers 1
Co-authored papers 1
Genomic Medicine Institute, Medical Research Center, Seoul National University
Co-authored papers 1
University of KwaZulu-Natal
Co-authored papers 1
Renaissance Computing Institute, University of North Carolina at Chapel Hill
Co-authored papers 1
Co-authored papers 1