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Steven McCarroll

Research Profile

Genes & Molecular Sequences

Physiology

Procedures

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Publications

TOP 3
Giulio Genovese; Robert E Handsaker; Heng Li; Amelia M Lindgren; Cynthia C Morton; Bogdan Pasaniuc; Martin R Pollak; Alkes L Price; David Reich; James G Wilson; Nicolas Altemose; Kimberly Chambert; Steven A McCarroll
Using population admixture to help complete maps of the human genome.
Jacob J Michaelson; Aine Peoples; Yujian Shi; Balvindar Singh; Jun Wang; Wenting Wu; Kun Zhang; Hancheng Zheng; Natacha Akshoomoff; Abhishek Bhandari; Roser Corominas; Christina Corsello; Jasper Estabillo; Therese Gadomski; Athurva Gore; Douglas Greer; Madhusudan Gujral; Lilia M Iakoucheva; Minghan Jian; Xin Jin; Shuli Kang; Amnon Koren; Yingrui Li; Guan Ning Lin; Guangming Liu; Dheeraj Malhotra; Steven A McCarroll; Jonathan Sebat
Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
Amnon Koren; Jacob J Michaelson; James Nemesh; Paz Polak; Jonathan Sebat; Shamil Sunyaev; Steven A McCarroll
Differential relationship of DNA replication timing to different forms of human mutation and variation.

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All Publications

2013: Giulio Genovese; Robert E Handsaker; Heng Li; Amelia M Lindgren; Cynthia C Morton; Bogdan Pasaniuc; Martin R Pollak; Alkes L Price; David Reich; James G Wilson; Nicolas Altemose; Kimberly Chambert; Steven A McCarroll
Using population admixture to help complete maps of the human genome.
Nature genetics 2013;45(4):406-14, 414e1-2.
2012: Jacob J Michaelson; Aine Peoples; Yujian Shi; Balvindar Singh; Jun Wang; Wenting Wu; Kun Zhang; Hancheng Zheng; Natacha Akshoomoff; Abhishek Bhandari; Roser Corominas; Christina Corsello; Jasper Estabillo; Therese Gadomski; Athurva Gore; Douglas Greer; Madhusudan Gujral; Lilia M Iakoucheva; Minghan Jian; Xin Jin; Shuli Kang; Amnon Koren; Yingrui Li; Guan Ning Lin; Guangming Liu; Dheeraj Malhotra; Steven A McCarroll; Jonathan Sebat
Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
Cell 2012;151(7):1431-42.
2012: Amnon Koren; Jacob J Michaelson; James Nemesh; Paz Polak; Jonathan Sebat; Shamil Sunyaev; Steven A McCarroll
Differential relationship of DNA replication timing to different forms of human mutation and variation.
American journal of human genetics 2012;91(6):1033-40.
2012: Menachem Fromer; Robert E Handsaker; Christina M Hultman; George Kirov; Steven A McCarroll; Jennifer L Moran; Michael C O'Donovan; Michael J Owen; Eric Banks; Sarah E Bergen; Kimberly Chambert; Douglas M Ruderfer; Pamela Sklar; Patrick F Sullivan; Shaun M Purcell
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.
American journal of human genetics 2012;91(4):597-607.
2012: Jacqueline I Goldstein; George B Grant; Christina M Hultman; Jared Maguire; Steven A McCarroll; Jennifer L Moran; Jason Carey; Kimberly Chambert; Andrew Crenshaw; Mark J Daly; Menachem Fromer; Colm O'Dushlaine; Shaun Purcell; Pamela Sklar; Christine Stevens; Patrick F Sullivan; Benjamin M Neale
zCall: a rare variant caller for array-based genotyping: genetics and population analysis.
Bioinformatics (Oxford, England) 2012;28(19):2543-5.
2012: S E Bergen; K D Chambert; R E Handsaker; Christina M Hultman; M Landen; P H Lee; P Lichtenstein; P K E Magnusson; Steven A McCarroll; J L Moran; Colm O'Dushlaine; Shaun Purcell; S Ripke; Douglas M Ruderfer; E M Scolnick; Pamela Sklar; S Akterin; L Backlund; Urban Osby; P F Sullivan
Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
Molecular psychiatry 2012;17(9):880-6.
2012: Linda M Boettger; Robert E Handsaker; Michael C Zody; Steven A McCarroll
Structural haplotypes and recent evolution of the human 17q21.31 region.
Nature genetics 2012;44(8):881-5.
2010: Soumya Raychaudhuri; Joshua M Korn; Steven A McCarroll; David Altshuler; Pamela Sklar; Shaun Purcell; Mark J Daly
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.
PLoS genetics 2010;6(9):.
2009: Steven A McCarroll; James E Bradner; Hannu Turpeinen; Liisa Volin; Paul J Martin; Shannon D Chilewski; Joseph H Antin; Stephanie J Lee; Tapani Ruutu; Barry Storer; Edus H Warren; Bo Zhang; Lue Ping Zhao; David Ginsburg; Robert J Soiffer; Jukka Partanen; John A Hansen; Jerome Ritz; Aarno Palotie; David Altshuler
Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease.
Nature genetics 2009;41(12):1341-4.
2008: Steven A McCarroll
Extending genome-wide association studies to copy-number variation.
Human molecular genetics 2008;17(R2):R135-42.
2007: Steven A McCarroll; David Altshuler
Copy-number variation and association studies of human disease.
Nature genetics 2007;39(7 Suppl):S37-42.
2007: Wendy Winckler; Michael Weedon; Robert R Graham; Steven A McCarroll; Shaun Purcell; Peter Almgren; Tiinamaija Tuomi; Daniel Gaudet; Kristina Bengtsson Boström; Mark Walker; Graham A Hitman; Andrew T Hattersley; Mark I McCarthy; Kristin G Ardlie; Joel N Hirschhorn; Mark J Daly; Timothy M Frayling; Leif Groop; David Altshuler
Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes.
Diabetes 2007;56(3):685-93.
2006: Devin P Locke; andrew sharp; Steven A McCarroll; Sean D McGrath; Tera Newman-Eerkes; Ze Cheng; Stuart Schwartz; Donna G Albertson; Daniel Pinkel; David Altshuler; Evan E Eichler
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.
American journal of human genetics 2006;79(2):275-90.
2006: Jennifer L Freeman; George H Perry; Lars Feuk; Richard Redon; Steven A McCarroll; David Altshuler; Hiroyuki Aburatani; Keith W Jones; Chris Tyler-Smith; Matthew E Hurles; Nigel P Carter; Stephen W Scherer; Charles Lee
Copy number variation: new insights in genome diversity.
Genome research 2006;16(8):949-61.
2006: Steven A McCarroll; Tracy N Hadnott; George H Perry; Pardis C Sabeti; Michael C Zody; Jeffrey C Barrett; Stephanie Dallaire; Stacey B Gabriel; Charles Lee; Mark J Daly; David Altshuler
Common deletion polymorphisms in the human genome.
Nature genetics 2006;38(1):86-92.