S. Stray

发表

Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.

T. Walsh, M. King, Ming K. Lee, 2006, JAMA.

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

A. Singleton, C. Baker, E. Eichler, 2008, Science.

Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

T. Walsh, M. King, Ming K. Lee, 2010, Proceedings of the National Academy of Sciences.

Spectrum of Mutations in BRCA 1 , BRCA 2 , CHEK 2 , and TP 53 in Families at High Risk of Breast Cancer

T. Walsh, M. King, Ming K. Lee, 2006 .

Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria

Michael S. Bereman, M. King, M. MacCoss, 2011, Proceedings of the National Academy of Sciences.

Mutations in Families at High Risk for Breast Cancer—Reply

M. King, Ming K. Lee, S. Casadei, 2006 .

Idiopathic hemochromatosis, an interim report.

S. Stray, J. Cook, C. Finch, 1980, Medicine.

Ferrokinetic measurement of erythropoiesis.

M. Cazzola, S. Stray, C. Finch, 1988, Acta haematologica.

Human platelet glycoprotein V: its role in enhancing expression of the glycoprotein Ib receptor.

S. Stray, G. Roth, D. Calverley, 1995, Blood.

The relationship between plasma iron and plasma iron turnover in the rat.

C. Finch, S. Stray, H. Huebers, 1981, Blood.

Three missense mutations in Arg codons of the factor VIII genes of mild to moderately severe hemophilia A patients.

A. Reiner, S. Stray, A. Thompson, 1992, Thrombosis research.

Plasma ferritin determination as a diagnostic tool.

S. Stray, J. Cook, M. Pippard, 1986, The Western journal of medicine.

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

Rochelle L. Garcia, T. Walsh, M. King, 2011, Proceedings of the National Academy of Sciences.

Loss of function germline mutations in RAD51D in women with ovarian carcinoma.

Rochelle L. Garcia, T. Walsh, M. King, 2012, Gynecologic oncology.

Reduced transcript expression of genes affected by inherited and de novo CNVs in autism

J. Sebat, D. Malhotra, T. Walsh, 2011, European Journal of Human Genetics.

Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer.

T. Walsh, M. King, J. Stamatoyannopoulos, 2011, Cancer research.

Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

C. Baker, T. Walsh, M. King, 2010, European Journal of Human Genetics.

Contribution of InheritedMutations in the BRCA 2-Interacting Protein PALB 2 to Familial Breast Cancer

T. Walsh, M. King, J. Stamatoyannopoulos, 2011 .

Iron supply for erythropoiesis in the rabbit.

C. Finch, S. Stray, M. Sivarajan, 1984, The Journal of clinical investigation.

Contribution of InheritedMutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer

T. Walsh, M. King, J. Stamatoyannopoulos, 2011 .

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

A. Singleton, E. Eichler, J. Sebat, 2008, Science.