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Items: 44

1.

Open Humans: A platform for participant-centered research and personal data exploration.

Greshake Tzovaras B, Angrist M, Arvai K, Dulaney M, Estrada-GaliƱanes V, Gunderson B, Head T, Lewis D, Nov O, Shaer O, Tzovara A, Bobe J, Price Ball M.

Gigascience. 2019 Jun 1;8(6). pii: giz076. doi: 10.1093/gigascience/giz076.

2.

Personal genomics: Where are we now?

Angrist M.

Appl Transl Genom. 2016 Feb 1;8:1-3. doi: 10.1016/j.atg.2016.01.010. eCollection 2016 Mar. No abstract available.

3.

Start me up: ways to encourage sharing of genomic information with research participants.

Angrist M.

Nat Rev Genet. 2015 Aug;16(8):435-6. doi: 10.1038/nrg3981.

PMID:
26184591
4.
5.

The audacity of interpretation: Protecting patients or piling on?

Angrist M.

Appl Transl Genom. 2014 Sep 1;3(3):68-69. No abstract available.

6.

Personalized medicine and human genetic diversity.

Lu YF, Goldstein DB, Angrist M, Cavalleri G.

Cold Spring Harb Perspect Med. 2014 Jul 24;4(9):a008581. doi: 10.1101/cshperspect.a008581. Review.

7.

Living laboratory: whole-genome sequencing as a learning healthcare enterprise.

Angrist M, Jamal L.

Clin Genet. 2015 Apr;87(4):311-8. doi: 10.1111/cge.12461. Epub 2014 Sep 6. Review.

8.

Open window: when easily identifiable genomes and traits are in the public domain.

Angrist M.

PLoS One. 2014 Mar 19;9(3):e92060. doi: 10.1371/journal.pone.0092060. eCollection 2014.

9.

Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes SEDT.

Davis EE, Savage JH, Willer JR, Jiang YH, Angrist M, Androutsopoulos A, Katsanis N.

Clin Genet. 2014 Apr;85(4):359-64. doi: 10.1111/cge.12189. Epub 2013 Jun 5.

PMID:
23656395
10.

Genetic privacy needs a more nuanced approach.

Angrist M.

Nature. 2013 Feb 7;494(7435):7. doi: 10.1038/494007a. No abstract available.

PMID:
23389508
11.

A public resource facilitating clinical use of genomes.

Ball MP, Thakuria JV, Zaranek AW, Clegg T, Rosenbaum AM, Wu X, Angrist M, Bhak J, Bobe J, Callow MJ, Cano C, Chou MF, Chung WK, Douglas SM, Estep PW, Gore A, Hulick P, Labarga A, Lee JH, Lunshof JE, Kim BC, Kim JI, Li Z, Murray MF, Nilsen GB, Peters BA, Raman AM, Rienhoff HY, Robasky K, Wheeler MT, Vandewege W, Vorhaus DB, Yang JL, Yang L, Aach J, Ashley EA, Drmanac R, Kim SJ, Li JB, Peshkin L, Seidman CE, Seo JS, Zhang K, Rehm HL, Church GM.

Proc Natl Acad Sci U S A. 2012 Jul 24;109(30):11920-7. doi: 10.1073/pnas.1201904109. Epub 2012 Jul 13.

13.

Urge overkill: protecting deidentified human subjects at what price?

Angrist M.

Am J Bioeth. 2010 Sep;10(9):17-8. doi: 10.1080/15265161.2010.494217. No abstract available.

PMID:
20818549
14.

DNA patents and diagnostics: not a pretty picture.

Carbone J, Gold ER, Sampat B, Chandrasekharan S, Knowles L, Angrist M, Cook-Deegan R.

Nat Biotechnol. 2010 Aug;28(8):784-91. doi: 10.1038/nbt0810-784. No abstract available.

15.

Impact of gene patents and licensing practices on access to genetic testing for long QT syndrome.

Angrist M, Chandrasekharan S, Heaney C, Cook-Deegan R.

Genet Med. 2010 Apr;12(4 Suppl):S111-54. doi: 10.1097/GIM.0b013e3181d68293.

16.

Personal genomes in progress: from the human genome project to the personal genome project.

Lunshof JE, Bobe J, Aach J, Angrist M, Thakuria JV, Vorhaus DB, Hoehe MR, Church GM.

Dialogues Clin Neurosci. 2010;12(1):47-60.

17.

Only connect: personal genomics and the future of American medicine.

Angrist M.

Mol Diagn Ther. 2010 Apr 1;14(2):67-72. doi: 10.2165/11534710-000000000-00000.

18.

We are the genes we've been waiting for: rational responses to the gathering storm of personal genomics.

Angrist M.

Am J Bioeth. 2009;9(6-7):30-1. doi: 10.1080/15265160902893999. No abstract available.

20.

The dangers of diagnostic monopolies.

Cook-Deegan R, Chandrasekharan S, Angrist M.

Nature. 2009 Mar 26;458(7237):405-6. doi: 10.1038/458405a. No abstract available.

21.

Public health. Genomics and medicine at a crossroads in Chernobyl.

Ginsburg GS, Angrist M, Cook-Deegan R.

Science. 2006 Oct 6;314(5796):62-3. No abstract available. Erratum in: Science. 2006 Dec 15;314(5806):1683.

PMID:
17023637
22.

Who owns the genome?

Angrist M, Cook-Deegan RM.

New Atlantis. 2006 Winter;11:87-96. No abstract available.

PMID:
16789312
23.
24.

Genomic medicine: genetic variation and its impact on the future of health care.

Willard HF, Angrist M, Ginsburg GS.

Philos Trans R Soc Lond B Biol Sci. 2005 Aug 29;360(1460):1543-50. Review.

25.

Breast cancer: integrating the patient with her genome.

Angrist M.

Trends Biotechnol. 2005 Jan;23(1):3-5. Review.

PMID:
15629848
26.

Segregation at three loci explains familial and population risk in Hirschsprung disease.

Gabriel SB, Salomon R, Pelet A, Angrist M, Amiel J, Fornage M, AttiƩ-Bitach T, Olson JM, Hofstra R, Buys C, Steffann J, Munnich A, Lyonnet S, Chakravarti A.

Nat Genet. 2002 May;31(1):89-93. Epub 2002 Apr 15.

PMID:
11953745
27.

Cloning of rat thymic stromal lymphopoietin receptor (TSLPR) and characterization of genomic structure of murine Tslpr gene.

Blagoev B, Nielsen MM, Angrist M, Chakravarti A, Pandey A.

Gene. 2002 Feb 6;284(1-2):161-8.

PMID:
11891057
28.

A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.

Bolk S, Pelet A, Hofstra RM, Angrist M, Salomon R, Croaker D, Buys CH, Lyonnet S, Chakravarti A.

Proc Natl Acad Sci U S A. 2000 Jan 4;97(1):268-73.

29.

The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome.

Southard-Smith EM, Angrist M, Ellison JS, Agarwala R, Baxevanis AD, Chakravarti A, Pavan WJ.

Genome Res. 1999 Mar;9(3):215-25.

30.

Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome 19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR.

Chadwick BP, Helbling LA, Angrist M, Chakravarti A, Gusella JF, Slaugenhaupt SA.

Cytogenet Cell Genet. 1998;83(3-4):236-7. No abstract available.

PMID:
10072588
31.

Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease.

Angrist M, Bolk S, Bentley K, Nallasamy S, Halushka MK, Chakravarti A.

Oncogene. 1998 Dec 10;17(23):3065-70.

32.

Less is more: compact genomes pay dividends.

Angrist M.

Genome Res. 1998 Jul;8(7):683-5. Review. No abstract available.

33.

Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility.

Angrist M, Jing S, Bolk S, Bentley K, Nallasamy S, Halushka M, Fox GM, Chakravarti A.

Genomics. 1998 Mar 15;48(3):354-62.

PMID:
9545641
34.

Does phaster mean better?

Angrist M.

Clin Chem. 1997 Mar;43(3):424-6. No abstract available.

35.

Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.

Angrist M, Bolk S, Halushka M, Lapchak PA, Chakravarti A.

Nat Genet. 1996 Nov;14(3):341-4.

PMID:
8896568
36.

Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome.

Bolk S, Angrist M, Xie J, Yanagisawa M, Silvestri JM, Weese-Mayer DE, Chakravarti A.

Nat Genet. 1996 Aug;13(4):395-6. No abstract available.

PMID:
8696331
37.

Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.

Bolk S, Angrist M, Schwartz S, Silvestri JM, Weese-Mayer DE, Chakravarti A.

Am J Med Genet. 1996 Jun 28;63(4):603-9.

PMID:
8826440
38.

A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome).

Hofstra RM, Osinga J, Tan-Sindhunata G, Wu Y, Kamsteeg EJ, Stulp RP, van Ravenswaaij-Arts C, Majoor-Krakauer D, Angrist M, Chakravarti A, Meijers C, Buys CH.

Nat Genet. 1996 Apr;12(4):445-7.

PMID:
8630503
39.

Chromosomal localization of the mouse Src-like adapter protein (Slap) gene and its putative human homolog SLA.

Angrist M, Wells DE, Chakravarti A, Pandey A.

Genomics. 1995 Dec 10;30(3):623-5.

PMID:
8825655
40.

Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.

Angrist M, Bolk S, Thiel B, Puffenberger EG, Hofstra RM, Buys CH, Cass DT, Chakravarti A.

Hum Mol Genet. 1995 May;4(5):821-30.

PMID:
7633441
41.

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.

Hentati A, Pericak-Vance MA, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist MH, Hung WY, Boustany RM, Bohlega S, et al.

Hum Mol Genet. 1994 Oct;3(10):1867-71.

PMID:
7849714
42.

Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22.

Puffenberger EG, Kauffman ER, Bolk S, Matise TC, Washington SS, Angrist M, Weissenbach J, Garver KL, Mascari M, Ladda R, et al.

Hum Mol Genet. 1994 Aug;3(8):1217-25.

PMID:
7987295
43.

A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.

Angrist M, Kauffman E, Slaugenhaupt SA, Matise TC, Puffenberger EG, Washington SS, Lipson A, Cass DT, Reyna T, Weeks DE, et al.

Nat Genet. 1993 Aug;4(4):351-6.

PMID:
8401581
44.

Autism resources at the higher education level in Indiana.

Dalrymple NJ, Angrist MH.

J Autism Dev Disord. 1989 Mar;19(1):173-5. No abstract available.

PMID:
2708299

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