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Author Details
Full Name
Misha Angrist
Affiliation
Duke University.
ORCID
Career Start Year
1989
Papers
47
H Index
18
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34704909
Stop the Madness: Dementia, "Radical Medicalization," and Straw Men.
AJOB Neurosci
2021
33095048
Reactions to the National Academies/Royal Society Report on <i>Heritable Human Genome Editing</i>.
CRISPR J
2020
33043412
Good problems to have? Policy and societal implications of a disease-modifying therapy for presymptomatic late-onset Alzheimer's disease.
Life Sci Soc Policy
2020
33052113
Participant-Partners in Genetic Research: An Exome Study with Families of Children with Unexplained Medical Conditions.
J Particip Med
2018
27047752
Personal genomics: Where are we now?
Appl Transl Genom
2016
25045831
Living laboratory: whole-genome sequencing as a learning healthcare enterprise.
Clin Genet
2015
26184591
Start me up: ways to encourage sharing of genomic information with research participants.
Nat Rev Genet
2015
23656395
Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes SEDT.
Clin Genet
2014
25621201
The audacity of interpretation: Protecting patients or piling on?
Appl Transl Genom
2014
25642409
Distributing the future: The weak justifications for keeping human genomic databases secret and the challenges and opportunities in reverse engineering them.
Appl Transl Genom
2014
25059740
Personalized medicine and human genetic diversity.
Cold Spring Harb Perspect Med
2014
24647311
Open window: when easily identifiable genomes and traits are in the public domain.
PLoS One
2014
23389508
Genetic privacy needs a more nuanced approach.
Nature
2013
22797899
A public resource facilitating clinical use of genomes.
Proc Natl Acad Sci U S A
2012
22199990
You never call, you never write: why return of 'omic' results to research participants is both a good idea and a moral imperative.
Per Med
2011
20373666
Personal genomes in progress: from the human genome project to the personal genome project.
Dialogues Clin Neurosci
2010
20818549
Urge overkill: protecting deidentified human subjects at what price?
Am J Bioeth
2010
20697400
DNA patents and diagnostics: not a pretty picture.
Nat Biotechnol
2010
20393304
Impact of gene patents and licensing practices on access to genetic testing for long QT syndrome.
Genet Med
2010
20359249
Only connect: personal genomics and the future of American medicine.
Mol Diagn Ther
2010
19325608
The dangers of diagnostic monopolies.
Nature
2009
22328898
Eyes wide open: the personal genome project, citizen science and veracity in informed consent.
Per Med
2009
19998110
We are the genes we've been waiting for: rational responses to the gathering storm of personal genomics.
Am J Bioeth
2009
16789312
Who owns the genome?
New Atlantis
2006
29793285
The future may be closer than you think: a response from the Personalized Medicine Coalition to the Royal Society's report on personalized medicine.
Per Med
2006
17023637
Public health. Genomics and medicine at a crossroads in Chernobyl.
Science
2006
15629848
Breast cancer: integrating the patient with her genome.
Trends Biotechnol
2005
16096102
Genomic medicine: genetic variation and its impact on the future of health care.
Philos Trans R Soc Lond B Biol Sci
2005
11891057
Cloning of rat thymic stromal lymphopoietin receptor (TSLPR) and characterization of genomic structure of murine Tslpr gene.
Gene
2002
11953745
Segregation at three loci explains familial and population risk in Hirschsprung disease.
Nat Genet
2002
10618407
A 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 A
2000
10077527
The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome.
Genome Res
1999
9685314
Less is more: compact genomes pay dividends.
Genome Res
1998
9881709
Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease.
Oncogene
1998
10072588
Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome 19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR.
Cytogenet Cell Genet
1998
9545641
Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility.
Genomics
1998
9068584
Does phaster mean better?
Clin Chem
1997
8630503
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome).
Nat Genet
1996
8896568
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
Nat Genet
1996
8826440
Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.
Am J Med Genet
1996
8696331
Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome.
Nat Genet
1996
7633441
Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.
Hum Mol Genet
1995
8825655
Chromosomal localization of the mouse Src-like adapter protein (Slap) gene and its putative human homolog SLA.
Genomics
1995
7849714
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.
Hum Mol Genet
1994
7987295
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22.
Hum Mol Genet
1994
8401581
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.
Nat Genet
1993
2708299
Autism resources at the higher education level in Indiana.
J Autism Dev Disord
1989
1 - 47 of 47
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