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Lethal Skeletal Dysplasia in Mice and Humans Lacking the Golgin GMAP-210SMITS, Patrick; BOLTON, Andrew D; MERRIMAN, Barry et al.The New England journal of medicine. 2010, Vol 362, Num 3, pp 206-216, issn 0028-4793, 11 p.Article

A mouse mutation in the 12R-lipoxygenase, Alox12b, disrupts formation of the epidermal permeability barrierMORAN, Jennifer L; HAIYAN QIU; TURBE-DOAN, Annick et al.Journal of investigative dermatology. 2007, Vol 127, Num 8, pp 1893-1897, issn 0022-202X, 5 p.Article

Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA SequenceGENOVESE, Giulio; KÄHLER, Anna K; PURCELL, Shaun M et al.The New England journal of medicine. 2014, Vol 371, Num 26, pp 2477-2487, issn 0028-4793, 11 p.Article

Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing DepthFROMER, Menachem; MORAN, Jennifer L; KIROV, George et al.American journal of human genetics. 2012, Vol 91, Num 4, pp 597-607, issn 0002-9297, 11 p.Article

Implication of a Rare Deletion at Distal 16p11.2 in SchizophreniaGUHA, Saurav; REES, Elliott; CICHON, Sven et al.JAMA psychiatry (Chicago, Ill. Print). 2013, Vol 70, Num 3, pp 253-260, issn 2168-622X, 8 p.Article

Exome sequencing and the genetic basis of complex traitsKIEZUN, Adam; GARIMELLA, Kiran; HULTMAN, Christina M et al.Nature genetics. 2012, Vol 44, Num 6, pp 623-630, issn 1061-4036, 8 p.Article

zCall: a rare variant caller for array-based genotypingGOLDSTEIN, Jacqueline I; CRENSHAW, Andrew; SCHIZOPHRENIA CONSORTIUM, Swedish et al.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 19, pp 2543-2545, issn 1367-4803, 3 p.Article

Bile Duct Proliferation in Jag1/Fringe Heterozygous Mice Identifies Candidate Modifiers of the Alagille Syndrome Hepatic PhenotypeRYAN, Matthew J; BALES, Christina; SPINNER, Nancy B et al.Hepatology (Baltimore, Md.). 2008, Vol 48, Num 6, pp 1989-1997, issn 0270-9139, 9 p.Article

Analysis of copy number variations at 15 schizophrenia-associated lociREES, Elliott; WALTERS, James T. R; O'DONOVAN, Michael C et al.British journal of psychiatry (Print). 2014, Vol 204, Num 2, pp 108-114, issn 0007-1250, 7 p.Article

Extremely low-coverage sequencing and imputation increases power for genome-wide association studiesPASANIUC, Bogdan; ROHLAND, Nadin; SULLIVAN, Patrick F et al.Nature genetics. 2012, Vol 44, Num 6, pp 631-635, issn 1061-4036, 5 p.Article

Rescue of the mouse DDK syndrome by parent-of-origin-dependent modifiersIDERAABDULLAH, Folami Y; KIM, Kuikwon; POMP, Daniel et al.Biology of reproduction. 2007, Vol 76, Num 2, pp 286-293, issn 0006-3363, 8 p.Article