Power calculations for genetic association studies using estimated probability distributionsSCHORK, Nicholas J.American journal of human genetics. 2002, Vol 70, Num 6, pp 1480-1489, issn 0002-9297Article

Distribution analysis of nonsynonymous polymorphisms within the human kinase gene familyTORKAMANI, Ali; SCHORK, Nicholas J.Genomics (San Diego, Calif.). 2007, Vol 90, Num 1, pp 49-58, issn 0888-7543, 10 p.Article

A simulation-based analysis of chromosome segment sharing among a group of arbitrarily related individualsLIBIGER, Ondrej; SCHORK, Nicholas J.European journal of human genetics. 2007, Vol 15, Num 12, pp 1260-1268, issn 1018-4813, 9 p.Article

Generalized genomic distance-based regression methodology for multilocus association analysisWESSEL, Jennifer; SCHORK, Nicholas J.American journal of human genetics. 2006, Vol 79, Num 5, pp 792-806, issn 0002-9297, 15 p.Article

Prediction of Cancer Driver Mutations in Protein KinasesTORKAMANI, Ali; SCHORK, Nicholas J.Cancer research (Baltimore). 2008, Vol 68, Num 6, pp 1675-1682, issn 0008-5472, 8 p.Article

Accurate prediction of deleterious protein kinase polymorphismsTORKAMANI, Ali; SCHORK, Nicholas J.Bioinformatics (Oxford. Print). 2007, Vol 23, Num 21, pp 2918-2925, issn 1367-4803, 8 p.Article

Prestige centrality-based functional outlier detection in gene expression analysisTORKAMANI, Ali; SCHORK, Nicholas J.Bioinformatics (Oxford. Print). 2009, Vol 25, Num 17, pp 2222-2228, issn 1367-4803, 7 p.Article

Predicting functional regulatory polymorphismsTORKAMANI, Ali; SCHORK, Nicholas J.Bioinformatics (Oxford. Print). 2008, Vol 24, Num 16, pp 1787-1792, issn 1367-4803, 6 p.Article

Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype dataFALLIN, Daniele; SCHORK, Nicholas J.American journal of human genetics. 2000, Vol 67, Num 4, pp 947-959, issn 0002-9297Article

Accommodating pathway information in expression quantitative trait locus analysisWESSEL, Jennifer; ZAPALA, Matthew A; SCHORK, Nicholas J et al.Genomics (San Diego, Calif.). 2007, Vol 90, Num 1, pp 132-142, issn 0888-7543, 11 p.Article

Inherent bias toward the null hypothesis in conventional multipoint nonparametric linkage analysisSCHORK, Nicholas J; GREENWOOD, Tiffany A.American journal of human genetics. 2004, Vol 74, Num 2, pp 306-316, issn 0002-9297, 11 p.Article

Gene-by-Environment (Serotonin Transporter and Childhood Maltreatment) Interaction for Anxiety Sensitivity, an Intermediate Phenotype for Anxiety DisordersSTEIN, Murray B; SCHORK, Nicholas J; GELERNTER, Joel et al.Neuropsychopharmacology (New York, NY). 2008, Vol 33, Num 2, pp 312-319, issn 0893-133X, 8 p.Article

Effect of Direct-to-Consumer Genomewide Profiling to Assess Disease RiskBLOSS, Cinnamon S; SCHORK, Nicholas J; TOPOL, EricJ et al.The New England journal of medicine. 2011, Vol 364, Num 6, pp 524-534, issn 0028-4793, 11 p.Article

A polymorphism of the β₁-adrenergic receptor is associated with low extraversionSTEIN, Murray B; SCHORK, Nicholas J; GELERNTER, Joel et al.Biological psychiatry (1969). 2004, Vol 56, Num 4, pp 217-224, issn 0006-3223, 8 p.Article

Accommodating Linkage Disequilibrium in Genetic-Association Analyses via Ridge RegressionMALO, Nathalie; LIBIGER, Ondrej; SCHORK, Nicholas J et al.American journal of human genetics. 2008, Vol 82, Num 2, pp 375-385, issn 0002-9297, 11 p.Article

Pathway analysis of seven common diseases assessed by genome-wide associationTORKAMANI, Ali; TOPOL, Eric J; SCHORK, Nicholas J et al.Genomics (San Diego, Calif.). 2008, Vol 92, Num 5, pp 265-272, issn 0888-7543, 8 p.Article

Statistical analysis strategies for association studies involving rare variantsBANSAL, Vikas; LIBIGER, Ondrej; TORKAMANI, Ali et al.Nature reviews. Genetics (Print). 2010, Vol 11, Num 11, pp 773-785, issn 1471-0056, 13 p.Article

Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjectsSCHORK, Nicholas J; NATH, Swapan K; FALLIN, Daniele et al.American journal of human genetics. 2000, Vol 67, Num 5, pp 1208-1218, issn 0002-9297Article

Statistical genetics concepts and approaches in schizophrenia and related neuropsychiatric research : The use of endophenotypes to deconstruct and understand the genetic architecture, neurobiology, and guide future treatments of the group of schizophreniasSCHORK, Nicholas J; GREENWOOD, Tiffany A; BRAFF, David L et al.Schizophrenia bulletin. 2007, Vol 33, Num 1, pp 95-104, issn 0586-7614, 10 p.Article

Mindscape: A convergent perspective on life, mind, consciousness and happinessNICULESCU, Alexander B; SCHORK, Nicholas J; SALOMON, Daniel R et al.Journal of affective disorders. 2010, Vol 123, Num 1-3, pp 1-8, issn 0165-0327, 8 p.Article

Kinase mutations in human disease: interpreting genotype-phenotype relationshipsLAHIRY, Piya; TORKAMANI, Ali; SCHORK, Nicholas J et al.Nature reviews. Genetics (Print). 2010, Vol 11, Num 1, pp 60-74, issn 1471-0056, 15 p.Article

The insulin gene VNTR is associated with fasting insulin levels and development of juvenile obesityLE STUNFF, Catherine; FALLIN, Daniele; SCHORK, Nicholas J et al.Nature genetics. 2000, Vol 26, Num 4, pp 444-446, issn 1061-4036Article

A common promoter variant of the leptin gene is associated with changes in the relationship between serum leptin and fat mass in obese girlsLE STUNFF, Catherine; LE BIHAN, Christine; SCHORK, Nicholas J et al.Diabetes (New York, NY). 2000, Vol 49, Num 12, pp 2196-2200, issn 0012-1797Article

Direct-to-consumer personalized genomic testingBLOSS, Cinnamon S; DARST, Burcu F; TOPOL, Eric J et al.Human molecular genetics (Print). 2011, Vol 20, Num 2, issn 0964-6906, R132-R141, NSArticle

Extremes of Unexplained Variation as a Phenotype An Efficient Approach for Genome-Wide Association Studies of Cardiovascular DiseaseLANKTREE, Matthew B; HEGELE, Robert A; SCHORK, Nicholas J et al.Circulation. Cardiovascular genetics (Print). 2010, Vol 3, Num 2, pp 215-221, issn 1942-325X, 7 p.Article