Quantifying the amount of missing information in genetic association studiesNICOLAE, Dan L.Genetic epidemiology. 2006, Vol 30, Num 8, pp 703-717, issn 0741-0395, 15 p.Article

Testing untyped alleles (TUNA)- : Applications to genome-wide association studiesNICOLAE, Dan L.Genetic epidemiology. 2006, Vol 30, Num 8, pp 718-727, issn 0741-0395, 10 p.Article

Association studies for untyped markers with TUNAXIAOQUAN WEN; NICOLAE, Dan L.Bioinformatics (Oxford. Print). 2008, Vol 24, Num 3, pp 435-437, issn 1367-4803, 3 p.Article

Estimating the mixing proportion in a semiparametric mixture modelSONG, Seongjoo; NICOLAE, Dan L; SONG, Jongwoo et al.Computational statistics & data analysis. 2010, Vol 54, Num 10, pp 2276-2283, issn 0167-9473, 8 p.Article

GEL : a novel genotype calling algorithm using empirical likelihoodNICOLAE, Dan L; XIAOLIN WU; MIYAKE, Kazuaki et al.Bioinformatics (Oxford. Print). 2006, Vol 22, Num 16, pp 1942-1947, issn 1367-4803, 6 p.Article

An Exponential Combination Procedure for Set-Based Association Tests in Sequencing StudiesCHEN, Lin S; LI HSU; GAMAZON, Eric R et al.American journal of human genetics. 2012, Vol 91, Num 6, pp 977-986, issn 0002-9297, 10 p.Article

On Sharing Quantitative Trait GWAS Results in an Era of Multiple-omics Data and the Limits of Genomic PrivacyHAE KYUNG IM; GAMAZON, Eric R; NICOLAE, Dan L et al.American journal of human genetics. 2012, Vol 90, Num 4, pp 591-598, issn 0002-9297, 8 p.Article

Maternal asthma and microRNA regulation of soluble HLA-G in the airwayNICODEMUS-JOHNSON, Jessie; LAXMAN, Bharathi; SOLWAY, Julian et al.Journal of allergy and clinical immunology. 2013, Vol 131, Num 6, pp 1496-1503, issn 0091-6749, 8 p.Article

Further replication studies of the EVE Consortium meta-analysis identifies 2 asthma risk loci in European AmericansMYERS, Rachel A; HIMES, Blanca E; GRAVES, Penelope E et al.Journal of allergy and clinical immunology. 2012, Vol 130, Num 6, pp 1294-1301, issn 0091-6749, 8 p.Article

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesisRIOUX, John D; XAVIER, Ramnik J; SHUGART, Yin Yao et al.Nature genetics. 2007, Vol 39, Num 5, pp 596-604, issn 1061-4036, 9 p.Article

Genome-wide association study of lung function phenotypes in a founder populationYAO, Tsung-Chieh; GAIXIN DU; LOISEL, Dagan A et al.Journal of allergy and clinical immunology. 2014, Vol 133, Num 1, pp 248-255, issn 0091-6749, 8 p.Article

Spoiling the Whole Bunch: Quality Control Aimed at Preserving the Integrity of High-Throughput GenotypingPLUZHNIKOV, Anna; BELOW, Jennifer E; KONKASHBAEV, Anuar et al.American journal of human genetics. 2010, Vol 87, Num 1, pp 123-128, issn 0002-9297, 6 p.Article

Increased Protein-Coding Mutations in the Mitochondrial Genome of African American Women With PreeclampsiaDING, David; SCOTT, Nicole M; LEVY, Shawn et al.Reproductive sciences (Thousand Oaks, Calif.). 2012, Vol 19, Num 12, pp 1343-1351, issn 1933-7191, 9 p.Article

Genome-wide meta-analysis for severe diabetic retinopathyGRASSI, Michael A; TIKHOMIROV, Anna; RAMALINGAM, Sudha et al.Human molecular genetics (Print). 2011, Vol 20, Num 12, pp 2472-2481, issn 0964-6906, 10 p.Article

Recombination rates in admixed individuals identified by ancestry-based inferenceWEGMANN, Daniel; KESSNER, Darren E; BECKER, Lewisc et al.Nature genetics. 2011, Vol 43, Num 9, pp 847-853, issn 1061-4036, 7 p.Article

Regulation of IL-8 and IL-1β expression in Crohn's disease associated NOD2/CARD15 mutationsJING LI; MORAN, Thomas; SWANSON, Eric et al.Human molecular genetics (Print). 2004, Vol 13, Num 16, pp 1715-1725, issn 0964-6906, 11 p.Article

A meta-analysis of genome-wide association studies for serum total IgE in diverse study populationsLEVIN, Albert M; MATHIAS, Rasika A; PARK, Julie E et al.Journal of allergy and clinical immunology. 2013, Vol 131, Num 4, pp 1176-1184, issn 0091-6749, 9 p.Article

Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13ALISKAN, Minal C; CHONG, Jessica X; MATERN, Dietrich et al.Human molecular genetics (Print). 2011, Vol 20, Num 7, pp 1285-1289, issn 0964-6906, 5 p.Article

Phenotype-stratified genetic linkage study demonstrates that IBD2 is an extensive ulcerative colitis locusACHKAR, Jean-Paul; DASSOPOULOS, Themistocles; LEILEI ZHANG et al.The American journal of gastroenterology. 2006, Vol 101, Num 3, pp 572-580, issn 0002-9270, 9 p.Article

A genome-wide association study identifies IL23R as an inflammatory bowel disease geneDUERR, Richard H; TAYLOR, Kent D; DASSOPOULOS, Themistocles et al.Science (Washington, D.C.). 2006, Vol 314, Num 5804, pp 1461-1463, issn 0036-8075, 3 p.Article

Rhinovirus Wheezing Illness and Genetic Risk of Childhood-Onset AsthmaCALISKAN, Minal; BOCHKOV, Yury A; NICOLAE, Dan L et al.The New England journal of medicine. 2013, Vol 368, Num 15, pp 1398-1407, issn 0028-4793, 10 p.Article

Finding Disease Variants in Mendelian Disorders By Using Sequence Data: Methods and ApplicationsIONITA-LAZA, Iuliana; MAKAROV, Vlad; YOON, Seungtai et al.American journal of human genetics. 2011, Vol 89, Num 6, pp 701-712, issn 0002-9297, 12 p.Article

SCAN: SNP and copy number annotationGAMAZON, Eric R; WEI ZHANG; KONKASHBAEV, Anuar et al.Bioinformatics (Oxford. Print). 2010, Vol 26, Num 2, pp 259-262, issn 1367-4803, 4 p.Article

Patient Self-Report of Prior Laser Treatment Reliably Indicates Presence of Severe Diabetic RetinopathyGRASSI, Michael A; MAZZULLA, D. Anthony; KNUDTSON, Michael D et al.American journal of ophthalmology. 2009, Vol 147, Num 3, pp 501-504, issn 0002-9394, 4 p.Article

Effect of Variation in CHI3L1 on Serum YKL-40 Level, Risk of Asthma, and Lung FunctionOBER, Carole; ZHENG TAN; LESTER, Lucille A et al.The New England journal of medicine. 2008, Vol 358, Num 16, pp 1682-1691, issn 0028-4793, 10 p.Article