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Misha Angrist

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Publications

TOP 3
Misha Angrist
Genetic privacy needs a more nuanced approach.
Misha Angrist
Urge overkill: protecting deidentified human subjects at what price?
Julia Carbone; E Richard Gold; Bhaven Sampat; Subhashini Chandrasekharan; Lori Knowles; Misha Angrist; Robert Cook-Deegan
DNA patents and diagnostics: not a pretty picture.

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All Publications

2013: Misha Angrist
Genetic privacy needs a more nuanced approach.
Nature 2013;494(7435):7.
2010: Misha Angrist
Urge overkill: protecting deidentified human subjects at what price?
The American journal of bioethics : AJOB 2010;10(9):17-8.
2010: Julia Carbone; E Richard Gold; Bhaven Sampat; Subhashini Chandrasekharan; Lori Knowles; Misha Angrist; Robert Cook-Deegan
DNA patents and diagnostics: not a pretty picture.
Nature biotechnology 2010;28(8):784-91.
2010: Misha Angrist; Subhashini Chandrasekharan; Christopher Heaney; Robert Cook-Deegan
Impact of gene patents and licensing practices on access to genetic testing for long QT syndrome.
Genetics in medicine : official journal of the American College of Medical Genetics 2010;12(4 Suppl):S111-54.
2010: Misha Angrist
Only connect: personal genomics and the future of American medicine.
Molecular diagnosis & therapy 2010;14(2):67-72.
2009: Robert Cook-Deegan; Subhashini Chandrasekharan; Misha Angrist
The dangers of diagnostic monopolies.
Nature 2009;458(7237):405-6.
2009: Misha Angrist
We are the genes we've been waiting for: rational responses to the gathering storm of personal genomics.
The American journal of bioethics : AJOB 2009;9(6-7):30-1.
2002: Stacey B Gabriel; Rémi Salomon; Anna Pelet; Misha Angrist; Jeanne Amiel; Myriam Fornage; Tania Attié-Bitach; Jane M Olson; Robert Hofstra; Charles Buys; Julie Steffann; Arnold Munnich; Stanislas LYONNET; Aravinda Chakravarti
Segregation at three loci explains familial and population risk in Hirschsprung disease.
Nature genetics 2002;31(1):89-93.
2000: S Bolk; Anna Pelet; R M Hofstra; Misha Angrist; Rémi Salomon; D Croaker; C H Buys; Stanislas LYONNET; Aravinda Chakravarti
A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(1):268-73.
1998: Misha Angrist; S Bolk; K Bentley; Sudha Nallasamy; Marc K Halushka; Aravinda Chakravarti
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;17(23):3065-70.
1998: Misha Angrist
Less is more: compact genomes pay dividends.
Genome research 1998;8(7):683-5.
1998: Misha Angrist; Shuqian Jing; S Bolk; K Bentley; Sudha Nallasamy; Marc K Halushka; GM Fox; Aravinda Chakravarti
Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility.
Genomics 1998;48(3):354-62.
1996: Misha Angrist; S Bolk; Marc K Halushka; P A Lapchak; Aravinda Chakravarti
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
Nature genetics 1996;14(3):341-4.
1996: S Bolk; Misha Angrist; J Xie; M Yanagisawa; Jean M Silvestri; Debra E Weese-Mayer; Aravinda Chakravarti
Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome.
Nature genetics 1996;13(4):395-6.
1996: S Bolk; Misha Angrist; Stuart Schwartz; Jean M Silvestri; Debra E Weese-Mayer; Aravinda Chakravarti
Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.
American journal of medical genetics 1996;63(4):603-9.
1996: Robert M W Hofstra; Jan Osinga; G Tan-Sindhunata; Ying Wu; E J Kamsteeg; Rein P Stulp; Conny van Ravenswaaij-Arts; D Majoor-Krakauer; Misha Angrist; Aravinda Chakravarti; Carel Meijers; Charles H C M Buys
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome).
Nature genetics 1996;12(4):445-7.
1995: Misha Angrist; D E Wells; Aravinda Chakravarti; Akhilesh Pandey
Chromosomal localization of the mouse Src-like adapter protein (Slap) gene and its putative human homolog SLA.
Genomics 1995;30(3):623-5.
1995: Misha Angrist; S Bolk; Bonnie A Thiel; Erik G Puffenberger; Robert M W Hofstra; Charles H C M Buys; D T Cass; Aravinda Chakravarti
Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.
Human molecular genetics 1995;4(5):821-30.
1994: Erik G Puffenberger; E R Kauffman; S Bolk; T C Matise; S S Washington; Misha Angrist; J Weissenbach; K L Garver; M Mascari; R Ladda
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22.
Human molecular genetics 1994;3(8):1217-25.
1993: Misha Angrist; E Kauffman; Susan A Slaugenhaupt; T C Matise; Erik G Puffenberger; S S Washington; A Lipson; D T Cass; T Reyna; Daniel E Weeks
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.
Nature genetics 1993;4(4):351-6.