Year |
Citation |
Score |
2022 |
Taub MA, Conomos MP, Keener R, Iyer KR, Weinstock JS, Yanek LR, Lane J, Miller-Fleming TW, Brody JA, Raffield LM, McHugh CP, Jain D, Gogarten SM, Laurie CA, Keramati A, ... ... Ruczinski I, et al. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2. PMID 35530816 DOI: 10.1016/j.xgen.2021.100084 |
0.326 |
|
2022 |
Ngwa JS, Yanek LR, Kammers K, Kanchan K, Taub MA, Scharpf RB, Faraday N, Becker LC, Mathias RA, Ruczinski I. Secondary analyses for genome-wide association studies using expression quantitative trait loci. Genetic Epidemiology. PMID 35312098 DOI: 10.1002/gepi.22448 |
0.335 |
|
2020 |
Cristiano S, McKean D, Carey J, Bracci P, Brennan P, Chou M, Du M, Gallinger S, Goggins MG, Hassan MM, Hung RJ, Kurtz RC, Li D, Lu L, Neale R, ... ... Ruczinski I, et al. Bayesian copy number detection and association in large-scale studies. Bmc Cancer. 20: 856. PMID 32894098 DOI: 10.1186/S12885-020-07304-3 |
0.342 |
|
2020 |
Bishop MR, Diaz Perez KK, Sun M, Ho S, Chopra P, Mukhopadhyay N, Hetmanski JB, Taub MA, Moreno-Uribe LM, Valencia-Ramirez LC, Restrepo Muñeton CP, Wehby G, Hecht JT, Deleyiannis F, Weinberg SM, ... ... Ruczinski I, et al. Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios. American Journal of Human Genetics. PMID 32574564 DOI: 10.1016/J.Ajhg.2020.05.018 |
0.363 |
|
2020 |
Kanchan K, Iyer K, Yanek LR, Carcamo-Orive I, Taub MA, Malley C, Baldwin K, Becker LC, Broeckel U, Cheng L, Cowan C, D'Antonio M, Frazer KA, Quertermous T, Mostoslavsky G, ... ... Ruczinski I, et al. Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen program. Stem Cell Research. 46: 101803. PMID 32442913 DOI: 10.1016/J.Scr.2020.101803 |
0.351 |
|
2020 |
Vince N, Limou S, Daya M, Morii W, Rafaels N, Geffard E, Douillard V, Walencik A, Boorgula MP, Chavan S, Vergara C, Ortega VE, Wilson JG, Lange LA, Watson H, ... ... Ruczinski I, et al. Association of HLA-DRB1*09:01 with tIgE levels among African ancestry individuals with asthma. The Journal of Allergy and Clinical Immunology. PMID 31981624 DOI: 10.1016/J.Jaci.2020.01.011 |
0.35 |
|
2019 |
Obeidat M, Faiz A, Li X, van den Berge M, Hansel NN, Joubert P, Hao K, Brandsma CA, Rafaels N, Mathias R, Ruczinski I, Beaty TH, Barnes KC, Paul Man SF, Paré PD, et al. The Pharmacogenomics of Inhaled Corticosteroids and Lung Function Decline in COPD. The European Respiratory Journal. PMID 31537701 DOI: 10.1183/13993003.00521-2019 |
0.352 |
|
2019 |
Daya M, Rafaels N, Brunetti TM, Chavan S, Levin AM, Shetty A, Gignoux CR, Boorgula MP, Wojcik G, Campbell M, Vergara C, Torgerson DG, Ortega VE, Doumatey A, Johnston HR, ... ... Ruczinski I, et al. Author Correction: Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations. Nature Communications. 10: 4082. PMID 31484942 DOI: 10.1038/S41467-019-12158-W |
0.318 |
|
2019 |
Boorgula MP, Taub MA, Rafaels N, Daya M, Campbell M, Chavan S, Shetty A, Cheadle C, Barkataki S, Fan J, David G, Beaty TH, Ruczinski I, Hanifin J, Schneider LC, et al. Replicated methylation changes associated with eczema herpeticum and allergic response. Clinical Epigenetics. 11: 122. PMID 31443688 DOI: 10.1186/S13148-019-0714-1 |
0.316 |
|
2019 |
Harris DN, Ruczinski I, Yanek LR, Becker LC, Becker DM, Guio H, Cui T, Chilton FH, Mathias RA, O'Connor TD. Evolution of Hominin Polyunsaturated Fatty Acid Metabolism: From Africa to the New World. Genome Biology and Evolution. PMID 30942856 DOI: 10.1093/Gbe/Evz071 |
0.323 |
|
2019 |
Winters A, Bahnson HT, Ruczinski I, Boorgula MP, Malley C, Keramati AR, Chavan S, Larson D, Cerosaletti K, Sayre PH, Plaut M, Du Toit G, Lack G, Barnes KC, Nepom GT, et al. The MALT1 locus and Peanut Avoidance in the Risk for Peanut Allergy. The Journal of Allergy and Clinical Immunology. PMID 30825465 DOI: 10.1016/J.Jaci.2019.02.016 |
0.308 |
|
2019 |
Daya M, Rafaels N, Brunetti TM, Chavan S, Levin AM, Shetty A, Gignoux CR, Boorgula MP, Wojcik G, Campbell M, Vergara C, Torgerson DG, Ortega VE, Doumatey A, Johnston HR, ... ... Ruczinski I, et al. Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations. Nature Communications. 10: 880. PMID 30787307 DOI: 10.1038/S41467-019-08469-7 |
0.36 |
|
2019 |
Wang AW, Avramopoulos D, Lori A, Mulle J, Conneely K, Powers A, Duncan E, Almli L, Massa N, McGrath J, Schwartz AC, Goes FS, Weng L, Wang R, Yolken R, ... Ruczinski I, et al. Genome-wide association study in two populations to determine genetic variants associated with Toxoplasma gondii infection and relationship to schizophrenia risk. Progress in Neuro-Psychopharmacology & Biological Psychiatry. PMID 30610941 DOI: 10.1016/J.Pnpbp.2018.12.019 |
0.382 |
|
2018 |
Sherman T, Fu J, Scharpf RB, Bureau A, Ruczinski I. Detection of rare disease variants in extended pedigrees using RVS. Bioinformatics (Oxford, England). PMID 30500888 DOI: 10.1093/Bioinformatics/Bty976 |
0.365 |
|
2018 |
Sherman RM, Forman J, Antonescu V, Puiu D, Daya M, Rafaels N, Boorgula MP, Chavan S, Vergara C, Ortega VE, Levin AM, Eng C, Yazdanbakhsh M, Wilson JG, Marrugo J, ... ... Ruczinski I, et al. Assembly of a pan-genome from deep sequencing of 910 humans of African descent. Nature Genetics. PMID 30455414 DOI: 10.1038/S41588-018-0273-Y |
0.33 |
|
2018 |
Bureau A, Begum F, Taub MA, Hetmanski JB, Parker MM, Albacha-Hejazi H, Scott AF, Murray JC, Marazita ML, Bailey-Wilson JE, Beaty TH, Ruczinski I. Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants. Genetic Epidemiology. PMID 30246882 DOI: 10.1002/Gepi.22155 |
0.391 |
|
2018 |
Qiao D, Ameli A, Prokopenko D, Chen H, Kho AT, Parker MM, Morrow J, Hobbs BD, Liu Y, Beaty TH, Crapo JD, Barnes KC, Nickerson DA, Bamshad M, Hersh CP, ... ... Ruczinski I, et al. Whole exome sequencing analysis in severe chronic obstructive pulmonary disease. Human Molecular Genetics. PMID 30060175 DOI: 10.1093/Hmg/Ddy269 |
0.405 |
|
2018 |
Sun X, Gao J, Jin P, Eng C, Burchard EG, Beaty TH, Ruczinski I, Mathias RA, Barnes KC, Wang F, Qin Z. Optimized distributed systems achieve significant performance improvement on sorted merging of massive VCF files. Gigascience. PMID 29762754 DOI: 10.1093/Gigascience/Giy052 |
0.311 |
|
2018 |
Reynolds LM, Howard TD, Ruczinski I, Kanchan K, Seeds MC, Mathias RA, Chilton FH. Tissue-specific impact of FADS cluster variants on FADS1 and FADS2 gene expression. Plos One. 13: e0194610. PMID 29590160 DOI: 10.1371/Journal.Pone.0194610 |
0.333 |
|
2018 |
Keramati AR, Yanek LR, Iyer K, Taub MA, Ruczinski I, Becker DM, Becker LC, Faraday N, Mathias RA. Targeted deep sequencing of the PEAR1 locus for platelet aggregation in European and African American families. Platelets. 30: 380-386. PMID 29553866 DOI: 10.1080/09537104.2018.1447659 |
0.302 |
|
2017 |
Obeidat M, Li X, Burgess S, Zhou G, Fishbane N, Hansel NN, Bossé Y, Joubert P, Hao K, Nickle DC, van den Berge M, Timens W, Cho MH, Hobbs BD, de Jong K, ... ... Ruczinski I, et al. Surfactant protein D is a causal risk factor for COPD: results of Mendelian randomisation. The European Respiratory Journal. 50. PMID 29191953 DOI: 10.1183/13993003.00657-2017 |
0.322 |
|
2017 |
Rahbar E, Ainsworth HC, Howard TD, Hawkins GA, Ruczinski I, Mathias R, Seeds MC, Sergeant S, Hixson JE, Herrington DM, Langefeld CD, Chilton FH. Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster. Plos One. 12: e0180903. PMID 28957329 DOI: 10.1371/Journal.Pone.0180903 |
0.371 |
|
2017 |
Yu Y, Zuo X, He M, Gao J, Fu Y, Qin C, Meng L, Wang W, Song Y, Cheng Y, Zhou F, Chen G, Zheng X, Wang X, Liang B, ... ... Ruczinski I, et al. Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity. Nature Communications. 8: 14364. PMID 28232668 DOI: 10.1038/Ncomms14364 |
0.381 |
|
2017 |
Qiao D, Lange C, Laird NM, Won S, Hersh CP, Morrow J, Hobbs BD, Lutz SM, Ruczinski I, Beaty TH, Silverman EK, Cho MH. Gene-based segregation method for identifying rare variants in family-based sequencing studies. Genetic Epidemiology. PMID 28191685 DOI: 10.1002/Gepi.22037 |
0.36 |
|
2017 |
Long X, Daya M, Zhao J, Rafaels N, Liang H, Potee J, Campbell M, Zhang B, Araujo MI, Oliveira RR, Mathias RA, Gao L, Ruczinski I, Georas SN, Vercelli D, et al. The role of ST2 and ST2 genetic variants in schistosomiasis. The Journal of Allergy and Clinical Immunology. PMID 28189770 DOI: 10.1016/J.Jaci.2016.12.969 |
0.357 |
|
2017 |
Wain LV, Shrine N, Artigas MS, Erzurumluoglu AM, Noyvert B, Bossini-Castillo L, Obeidat M, Henry AP, Portelli MA, Hall RJ, Billington CK, Rimington TL, Fenech AG, John C, Blake T, ... ... Ruczinski I, et al. Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. Nature Genetics. PMID 28166213 DOI: 10.1038/Ng.3787 |
0.356 |
|
2017 |
Mathias RA, Chavan S, Boorgula M, Cookson WO, Willis-Owen S, Rafaels NM, Hanifin JM, Paller A, Schneider LC, Gallo R, Guttman-Yassky E, Ong PY, Ruczinski I, Beaty T, Gao L, et al. Whole Genome Sequencing Identifies Four Novel Variants in the Epidermal Differentiation Complex That Increase Risk and Severity for Atopic Dermatitis Journal of Allergy and Clinical Immunology. 139: AB85. DOI: 10.1016/J.Jaci.2016.12.229 |
0.345 |
|
2017 |
Lori A, Avramopoulos D, Wang A, Goes FS, Mulle J, Powers A, McGrath JJ, Massa N, Weng L, Duncan E, Nestadt G, Conneely K, Wolyniec P, Wang R, Hopkins M, ... Ruczinski I, et al. 917. Genome-Wide Association Study (GWAS) of Toxoplasma Gondii Infection and Evaluation of Schizophrenia Risk by Using a Polygenic Risk Score (PRS) Biological Psychiatry. 81. DOI: 10.1016/J.Biopsych.2017.02.643 |
0.314 |
|
2016 |
Xiao Y, Taub MA, Ruczinski I, Begum F, Hetmanski JB, Schwender H, Leslie EJ, Koboldt DC, Murray JC, Marazita ML, Beaty TH. Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios. Genetic Epidemiology. PMID 28019042 DOI: 10.1002/Gepi.22023 |
0.428 |
|
2016 |
Fu J, Beaty TH, Scott AF, Hetmanski J, Parker MM, Wilson JE, Marazita ML, Mangold E, Albacha-Hejazi H, Murray JC, Bureau A, Carey J, Cristiano S, Ruczinski I, Scharpf RB. Whole exome association of rare deletions in multiplex oral cleft families. Genetic Epidemiology. PMID 27910131 DOI: 10.1002/Gepi.22010 |
0.34 |
|
2016 |
Mathias RA, Taub MA, Gignoux CR, Fu W, Musharoff S, O'Connor TD, Vergara C, Torgerson DG, Pino-Yanes M, Shringarpure SS, Huang L, Rafaels N, Boorgula MP, Johnston HR, Ortega VE, ... ... Ruczinski I, et al. A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome. Nature Communications. 7: 12522. PMID 27725671 DOI: 10.1038/Ncomms12522 |
0.358 |
|
2016 |
Kessler MD, Yerges-Armstrong L, Taub MA, Shetty AC, Maloney K, Jeng LJ, Ruczinski I, Levin AM, Williams LK, Beaty TH, Mathias RA, Barnes KC, O'Connor TD. Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry. Nature Communications. 7: 12521. PMID 27725664 DOI: 10.1038/Ncomms12521 |
0.371 |
|
2016 |
Begum F, Ruczinski I, Hokanson JE, Lutz SM, Parker MM, Cho MH, Hetmanski JB, Scharpf RB, Crapo JD, Silverman EK, Beaty TH. Hemizygous Deletion on Chromosome 3p26.1 Is Associated with Heavy Smoking among African American Subjects in the COPDGene Study. Plos One. 11: e0164134. PMID 27711239 DOI: 10.1371/Journal.Pone.0164134 |
0.368 |
|
2016 |
Mathias RA, Boorgula M, Chavan S, Iyer KR, Rafaels NM, Potee J, Hanifin JM, Paller AS, Schneider LC, Gallo RL, Guttman-Yassky E, Ong PY, Ruczinski I, Beaty TH, Gao L, et al. Filaggrin Associated Risk for Atopic Dermatitis Is Offset By Protective Missense Variants in Rptn and LCE1B Genes in the Epidermal Differentiation Complex Journal of Allergy and Clinical Immunology. 137: AB182. DOI: 10.1016/J.Jaci.2015.12.728 |
0.341 |
|
2015 |
Begum F, Ruczinski I, Li S, Silverman EK, Cho MH, Lynch DA, Curran-Everett D, Crapo J, Scharpf RB, Parker MM, Hetmanski JB, Beaty TH. Identifying a Deletion Affecting Total Lung Capacity Among Subjects in the COPDGene Study Cohort. Genetic Epidemiology. PMID 26643968 DOI: 10.1002/Gepi.21943 |
0.437 |
|
2015 |
Gao L, Emond MJ, Louie T, Cheadle C, Berger AE, Rafaels N, Vergara C, Kim Y, Taub MA, Ruczinski I, Mathai SC, Rich SS, Nickerson DA, Hummers LK, Bamshad MJ, et al. Whole-exome sequencing identifies rare variants in ATP8B4 as a risk factor for systemic sclerosis. Arthritis & Rheumatology (Hoboken, N.J.). PMID 26473621 DOI: 10.1002/Art.39449 |
0.313 |
|
2015 |
Gao L, Bin L, Rafaels NM, Huang L, Potee J, Ruczinski I, Beaty TH, Paller AS, Schneider LC, Gallo R, Hanifin JM, Beck LA, Geha RS, Mathias RA, Barnes KC, et al. Targeted deep sequencing identifies rare loss-of-function variants in IFNGR1 for risk of atopic dermatitis complicated by eczema herpeticum. The Journal of Allergy and Clinical Immunology. PMID 26343451 DOI: 10.1016/J.Jaci.2015.06.047 |
0.395 |
|
2015 |
Long X, Chen Q, Zhao J, Rafaels N, Mathias P, Liang H, Potee J, Campbell M, Zhang B, Gao L, Georas SN, Vercelli D, Beaty TH, Ruczinski I, Mathias R, et al. An IL-13 Promoter Polymorphism Associated with Liver Fibrosis in Patients with Schistosoma japonicum. Plos One. 10: e0135360. PMID 26258681 DOI: 10.1371/Journal.Pone.0135360 |
0.333 |
|
2015 |
Goes FS, McGrath J, Avramopoulos D, Wolyniec P, Pirooznia M, Ruczinski I, Nestadt G, Kenny EE, Vacic V, Peters I, Lencz T, Darvasi A, Mulle JG, Warren ST, Pulver AE. Genome-wide association study of schizophrenia in Ashkenazi Jews. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 168: 649-59. PMID 26198764 DOI: 10.1002/Ajmg.B.32349 |
0.391 |
|
2015 |
Avramopoulos D, Pearce BD, McGrath J, Wolyniec P, Wang R, Eckart N, Hatzimanolis A, Goes FS, Nestadt G, Mulle J, Coneely K, Hopkins M, Ruczinski I, Yolken R, Pulver AE. Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation. Plos One. 10: e0116696. PMID 25781172 DOI: 10.1371/Journal.Pone.0116696 |
0.41 |
|
2015 |
Younkin SG, Scharpf RB, Schwender H, Parker MM, Scott AF, Marazita ML, Beaty TH, Ruczinski I. A genome-wide study of inherited deletions identified two regions associated with nonsyndromic isolated oral clefts. Birth Defects Research. Part a, Clinical and Molecular Teratology. 103: 276-83. PMID 25776870 DOI: 10.1002/Bdra.23362 |
0.327 |
|
2015 |
Leslie EJ, Taub MA, Liu H, Steinberg KM, Koboldt DC, Zhang Q, Carlson JC, Hetmanski JB, Wang H, Larson DE, Fulton RS, Kousa YA, Fakhouri WD, Naji A, Ruczinski I, et al. Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci. American Journal of Human Genetics. 96: 397-411. PMID 25704602 DOI: 10.1016/J.Ajhg.2015.01.004 |
0.376 |
|
2015 |
Dluzniewski PJ, Xu J, Ruczinski I, Isaacs WB, Platz EA. Polymorphisms influencing prostate-specific antigen concentration may bias genome-wide association studies on prostate cancer. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 24: 88-93. PMID 25352524 DOI: 10.1158/1055-9965.Epi-14-0863 |
0.349 |
|
2015 |
Mathias RA, Chavan S, Iyer KR, Rafaels NM, Boorgula M, Potee J, Hanifin JM, Paller A, Schneider LC, Gallo RL, Guttman-Yassky E, Ong PY, Ruczinski I, Beaty TH, Gao L, et al. Identifying Genetic Determinants of Atopic Dermatitis and Bacterial Colonization Using Whole Genome Sequencing Journal of Allergy and Clinical Immunology. 135: AB391. DOI: 10.1016/J.Jaci.2014.12.1903 |
0.363 |
|
2015 |
Rafaels NM, Johnston HR, Huang L, Chavan S, Wilson JG, Williams LK, Ware LB, Ober C, Meyers DA, Hartert TV, Foreman M, Ford JG, Burchard EG, Bleecker ER, Taub M, ... ... Ruczinski I, et al. How Well Does Whole Genome Sequencing Improve Ability to Detect Association with Asthma in Candidate Genes Compared to Existing GWAS Platforms in African American Populations? Journal of Allergy and Clinical Immunology. 135: AB164. DOI: 10.1016/J.Jaci.2014.12.1473 |
0.379 |
|
2015 |
Masuko H, Rafaels NM, Huang L, Chavan S, Wilson JG, Williams LK, Ware LB, Ober C, Meyers DA, Hartert TV, Foreman M, Ford JG, Burchard EG, Bleecker ER, Dunston G, ... ... Ruczinski I, et al. Imputation from 328 African Ancestry Genomes Reveals New Associations with Asthma in DPP10 Journal of Allergy and Clinical Immunology. 135: AB162. DOI: 10.1016/J.Jaci.2014.12.1469 |
0.339 |
|
2014 |
Hansel NN, Paré PD, Rafaels N, Sin D, Sandford A, Daley D, Vergara C, Huang L, Elliott WM, Pascoe CD, Arsenault BA, Postma DS, Boezen HM, Bossé Y, van den Berge M, ... ... Ruczinski I, et al. Genome Wide Association Study Identifies Novel Loci Associated with Airway Responsiveness in COPD. American Journal of Respiratory Cell and Molecular Biology. PMID 25514360 DOI: 10.1165/Rcmb.2014-0198Oc |
0.397 |
|
2014 |
Neumann C, Taub MA, Younkin SG, Beaty TH, Ruczinski I, Schwender H. Analytic power and sample size calculation for the genotypic transmission/disequilibrium test in case-parent trio studies. Biometrical Journal. Biometrische Zeitschrift. 56: 1076-92. PMID 25123830 DOI: 10.1002/Bimj.201300148 |
0.337 |
|
2014 |
Schwender H, Li Q, Neumann C, Taub MA, Younkin SG, Berger P, Scharpf RB, Beaty TH, Ruczinski I. Detecting disease variants in case-parent trio studies using the bioconductor software package trio. Genetic Epidemiology. 38: 516-22. PMID 25048299 DOI: 10.1002/Gepi.21836 |
0.352 |
|
2014 |
Scharpf RB, Mireles L, Yang Q, Köttgen A, Ruczinski I, Susztak K, Halper-Stromberg E, Tin A, Cristiano S, Chakravarti A, Boerwinkle E, Fox CS, Coresh J, Linda Kao WH. Copy number polymorphisms near SLC2A9 are associated with serum uric acid concentrations. Bmc Genetics. 15: 81. PMID 25007794 DOI: 10.1186/1471-2156-15-81 |
0.398 |
|
2014 |
Tang W, Kowgier M, Loth DW, Soler Artigas M, Joubert BR, Hodge E, Gharib SA, Smith AV, Ruczinski I, Gudnason V, Mathias RA, Harris TB, Hansel NN, Launer LJ, Barnes KC, et al. Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function. Plos One. 9: e100776. PMID 24983941 DOI: 10.1371/Journal.Pone.0100776 |
0.394 |
|
2014 |
Bureau A, Parker MM, Ruczinski I, Taub MA, Marazita ML, Murray JC, Mangold E, Noethen MM, Ludwig KU, Hetmanski JB, Bailey-Wilson JE, Cropp CD, Li Q, Szymczak S, Albacha-Hejazi H, et al. Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts. Genetics. 197: 1039-44. PMID 24793288 DOI: 10.1534/Genetics.114.165225 |
0.391 |
|
2014 |
Bureau A, Younkin SG, Parker MM, Bailey-Wilson JE, Marazita ML, Murray JC, Mangold E, Albacha-Hejazi H, Beaty TH, Ruczinski I. Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bioinformatics (Oxford, England). 30: 2189-96. PMID 24740360 DOI: 10.1093/Bioinformatics/Btu198 |
0.358 |
|
2014 |
Younkin SG, Scharpf RB, Schwender H, Parker MM, Scott AF, Marazita ML, Beaty TH, Ruczinski I. A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk. Bmc Genetics. 15: 24. PMID 24528994 DOI: 10.1186/1471-2156-15-24 |
0.352 |
|
2014 |
Wu T, Schwender H, Ruczinski I, Murray JC, Marazita ML, Munger RG, Hetmanski JB, Parker MM, Wang P, Murray T, Taub M, Li S, Redett RJ, Fallin MD, Liang KY, et al. Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate. Plos One. 9: e88088. PMID 24516586 DOI: 10.1371/Journal.Pone.0088088 |
0.436 |
|
2014 |
Mathias RA, Huang L, Vergara CI, Gao L, Rafaels NM, Potee J, Campbell M, Masuko H, Fert-Bober J, Snider J, Taub M, Ruczinski I, Beaty TH, Van Eyk JE, Barnes KC. Sequencing Of The ST2 Gene and The Identification Of Genetic Determinants Of Serum Total ST2 Levels: Strong Evidence For Replication Across European and African American Populations Journal of Allergy and Clinical Immunology. 133: AB247. DOI: 10.1016/J.Jaci.2013.12.878 |
0.405 |
|
2014 |
Keet C, Hong X, Ruczinski I, Beaty TH, Pongracic J, Wang X. Genome-Wide Study Of Interaction Between Season Of Birth and Peanut Allergy Identifies a Region On Chromosome 3 As a Genetic Risk Factor Journal of Allergy and Clinical Immunology. 133: AB199. DOI: 10.1016/J.Jaci.2013.12.715 |
0.349 |
|
2014 |
Rafaels NM, Huang L, Leung DY, Beck LA, Vergara CI, Boguniewicz M, Hata T, Schneider LC, Hanifin JM, Gallo R, Gao L, Ruczinski I, Mathias RA, Barnes KC. Exome Chip Genotyping Reveals Association With PDE4C and Atopic Dermatitis In Populations Of European and African Descent Journal of Allergy and Clinical Immunology. 133: AB72. DOI: 10.1016/J.Jaci.2013.12.280 |
0.35 |
|
2013 |
Taub MA, Schwender HR, Younkin SG, Louis TA, Ruczinski I. On multi-marker tests for association in case-control studies. Frontiers in Genetics. 4: 252. PMID 24379823 DOI: 10.3389/Fgene.2013.00252 |
0.368 |
|
2013 |
Stephens SH, Hartz SM, Hoft NR, Saccone NL, Corley RC, Hewitt JK, Hopfer CJ, Breslau N, Coon H, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, Han Y, ... ... Ruczinski I, et al. Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genetic Epidemiology. 37: 846-59. PMID 24186853 DOI: 10.1002/Gepi.21760 |
0.346 |
|
2013 |
Vergara C, Murray T, Rafaels N, Lewis R, Campbell M, Foster C, Gao L, Faruque M, Oliveira RR, Carvalho E, Araujo MI, Cruz AA, Watson H, Mercado D, Knight-Madden J, ... Ruczinski I, et al. African ancestry is a risk factor for asthma and high total IgE levels in African admixed populations. Genetic Epidemiology. 37: 393-401. PMID 23554133 DOI: 10.1002/Gepi.21702 |
0.333 |
|
2013 |
Li Q, Schwender H, Louis TA, Fallin MD, Ruczinski I. Efficient simulation of epistatic interactions in case-parent trios. Human Heredity. 75: 12-22. PMID 23548797 DOI: 10.1159/000348789 |
0.382 |
|
2013 |
Beaty TH, Taub MA, Scott AF, Murray JC, Marazita ML, Schwender H, Parker MM, Hetmanski JB, Balakrishnan P, Mansilla MA, Mangold E, Ludwig KU, Noethen MM, Rubini M, Elcioglu N, ... Ruczinski I, et al. Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study. Human Genetics. 132: 771-81. PMID 23512105 DOI: 10.1007/S00439-013-1283-6 |
0.429 |
|
2013 |
Patel PJ, Beaty TH, Ruczinski I, Murray JC, Marazita ML, Munger RG, Hetmanski JB, Wu T, Murray T, Rose M, Redett RJ, Jin SC, Lie RT, Wu-Chou YH, Wang H, et al. X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts. European Journal of Oral Sciences. 121: 63-8. PMID 23489894 DOI: 10.1111/Eos.12025 |
0.446 |
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2013 |
Omoumi A, Wang Z, Yeow V, Wu-Chou YH, Chen PK, Ruczinski I, Cheng J, Cheah FS, Lee CG, Beaty TH, Chong SS. Fetal polymorphisms at the ABCB1-transporter gene locus are associated with susceptibility to non-syndromic oral cleft malformations. European Journal of Human Genetics : Ejhg. 21: 1436-41. PMID 23443032 DOI: 10.1038/Ejhg.2013.25 |
0.401 |
|
2013 |
Alberg AJ, Jorgensen TJ, Ruczinski I, Wheless L, Shugart YY, Berthier-Schaad Y, Kessing B, Hoffman-Bolton J, Helzlsouer KJ, Kao WH, Francis L, Alani RM, Smith MW, Strickland PT. DNA repair gene variants in relation to overall cancer risk: a population-based study. Carcinogenesis. 34: 86-92. PMID 23027618 DOI: 10.1093/Carcin/Bgs304 |
0.379 |
|
2013 |
Hansel NN, Ruczinski I, Rafaels N, Sin DD, Daley D, Malinina A, Huang L, Sandford A, Murray T, Kim Y, Vergara C, Heckbert SR, Psaty BM, Li G, Elliott WM, et al. Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD. Human Genetics. 132: 79-90. PMID 22986903 DOI: 10.1007/S00439-012-1219-6 |
0.415 |
|
2013 |
Wang H, Zhang T, Wu T, Hetmanski JB, Ruczinski I, Schwender H, Liang KY, Murray T, Fallin MD, Redett RJ, Raymond GV, Jin SC, Chou YH, Chen PK, Yeow V, et al. The FGF and FGFR Gene Family and Risk of Cleft Lip With or Without Cleft Palate. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 50: 96-103. PMID 22074045 DOI: 10.1597/11-132 |
0.355 |
|
2013 |
Hedjoudje A, Huang L, Rafaels NM, Vergara CI, Taub M, Ruczinski I, Ober C, Burchard EG, Beaty TH, Vercelli D, Barnes KC, Mathias RA. Whole Genome Sequence Reveals a Haplotype Conferring Protection From Asthma Common to Subjects of European and African Ancestry Journal of Allergy and Clinical Immunology. 131: AB54. DOI: 10.1016/J.Jaci.2012.12.874 |
0.335 |
|
2013 |
Huang L, Gao L, Figueiredo C, Rafaels NM, Vergara CI, Ruczinski I, Beaty TH, Barnes KC, Mathias RA. Sequencing of the ST2 Gene Reveals a Haplotype That Determines Serum Total ST2 Levels in Individuals of African Ancestry Journal of Allergy and Clinical Immunology. 131: AB53. DOI: 10.1016/J.Jaci.2012.12.873 |
0.312 |
|
2013 |
Mathias RA, Huang L, Gao L, Rafaels NM, Vergara CI, Ruczinski I, Beaty TH, Barnes KC. Targeted Deep Resequencing of Thirteen Candidate Genes Reveals Novel Variants Determining Asthma Risk in Individuals of African Ancestry Journal of Allergy and Clinical Immunology. 131: AB159. DOI: 10.1016/J.Jaci.2012.12.1228 |
0.351 |
|
2013 |
Masuko H, Gao L, Rafaels NM, Vergara CI, Huang L, Campbell M, Ruczinski I, Beaty TH, Oliveira R, Cruz AA, Carvalho EM, Mathias RA, Araujo MI, Barnes KC. Novel IL33 Gene Polymorphisms Associated with Asthma Are Associated with Resistance to Schistosoma Mansoni Journal of Allergy and Clinical Immunology. 131: AB138. DOI: 10.1016/J.Jaci.2012.12.1159 |
0.328 |
|
2012 |
Scharpf RB, Beaty TH, Schwender H, Younkin SG, Scott AF, Ruczinski I. Fast detection of de novo copy number variants from SNP arrays for case-parent trios. Bmc Bioinformatics. 13: 330. PMID 23234608 DOI: 10.1186/1471-2105-13-330 |
0.338 |
|
2012 |
Hartz SM, Short SE, Saccone NL, Culverhouse R, Chen L, Schwantes-An TH, Coon H, Han Y, Stephens SH, Sun J, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, ... ... Ruczinski I, et al. Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Archives of General Psychiatry. 69: 854-60. PMID 22868939 DOI: 10.1001/Archgenpsychiatry.2012.124 |
0.312 |
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2012 |
Ludwig KU, Mangold E, Herms S, Nowak S, Reutter H, Paul A, Becker J, Herberz R, AlChawa T, Nasser E, Böhmer AC, Mattheisen M, Alblas MA, Barth S, Kluck N, ... ... Ruczinski I, et al. Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nature Genetics. 44: 968-71. PMID 22863734 DOI: 10.1038/Ng.2360 |
0.39 |
|
2012 |
Taub MA, Schwender H, Beaty TH, Louis TA, Ruczinski I. Incorporating genotype uncertainties into the genotypic TDT for main effects and gene-environment interactions. Genetic Epidemiology. 36: 225-34. PMID 22678881 DOI: 10.1002/Gepi.21615 |
0.388 |
|
2012 |
Jorgensen TJ, Ruczinski I, Yao Shugart Y, Wheless L, Berthier Schaad Y, Kessing B, Hoffman-Bolton J, Helzlsouer KJ, Kao WH, Francis L, Alani RM, Strickland PT, Smith MW, Alberg AJ. A population-based study of hedgehog pathway gene variants in relation to the dual risk of basal cell carcinoma plus another cancer. Cancer Epidemiology. 36: e288-93. PMID 22677152 DOI: 10.1016/J.Canep.2012.05.001 |
0.329 |
|
2012 |
Ruczinski I, Jorgensen TJ, Shugart YY, Schaad YB, Kessing B, Hoffman-Bolton J, Helzlsouer KJ, Kao WH, Wheless L, Francis L, Alani RM, Strickland PT, Smith MW, Alberg AJ. A population-based study of DNA repair gene variants in relation to non-melanoma skin cancer as a marker of a cancer-prone phenotype. Carcinogenesis. 33: 1692-8. PMID 22581838 DOI: 10.1093/Carcin/Bgs170 |
0.384 |
|
2012 |
Laurie CC, Laurie CA, Rice K, Doheny KF, Zelnick LR, McHugh CP, Ling H, Hetrick KN, Pugh EW, Amos C, Wei Q, Wang LE, Lee JE, Barnes KC, Hansel NN, ... ... Ruczinski I, et al. Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nature Genetics. 44: 642-50. PMID 22561516 DOI: 10.1038/Ng.2271 |
0.333 |
|
2012 |
Chen Q, Wang H, Hetmanski JB, Zhang T, Ruczinski I, Schwender H, Liang KY, Fallin MD, Redett RJ, Raymond GV, Wu Chou YH, Chen PK, Yeow V, Chong SS, Cheah FS, et al. BMP4 was associated with NSCL/P in an Asian population. Plos One. 7: e35347. PMID 22514733 DOI: 10.1371/Journal.Pone.0035347 |
0.428 |
|
2012 |
Murray T, Taub MA, Ruczinski I, Scott AF, Hetmanski JB, Schwender H, Patel P, Zhang TX, Munger RG, Wilcox AJ, Ye X, Wang H, Wu T, Wu-Chou YH, Shi B, et al. Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and Europeans. Genetic Epidemiology. 36: 392-9. PMID 22508319 DOI: 10.1002/Gepi.21633 |
0.413 |
|
2012 |
Zhang TX, Beaty TH, Ruczinski I. Candidate pathway based analysis for cleft lip with or without cleft palate. Statistical Applications in Genetics and Molecular Biology. 11. PMID 22499695 DOI: 10.2202/1544-6115.1717 |
0.356 |
|
2012 |
Wang H, Hetmanski JB, Ruczinski I, Liang KY, Fallin MD, Redett RJ, Raymond GV, Chou YH, Chen PK, Yeow V, Chong SS, Cheah FSh, Jabs EW, Scott AF, Beaty TH. ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population. Chinese Medical Journal. 125: 476-80. PMID 22490406 DOI: 10.3760/Cma.J.Issn.0366-6999.2012.03.014 |
0.41 |
|
2012 |
Shi M, Murray JC, Marazita ML, Munger RG, Ruczinski I, Hetmanski JB, Wu T, Murray T, Redett RJ, Wilcox AJ, Lie RT, Jabs EW, Wu-Chou YH, Chen PK, Wang H, et al. Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts. American Journal of Medical Genetics. Part A. 158: 784-94. PMID 22419666 DOI: 10.1002/Ajmg.A.35257 |
0.424 |
|
2012 |
Wheless L, Kistner-Griffin E, Jorgensen TJ, Ruczinski I, Berthier-Schaad Y, Kessing B, Hoffman-Bolton J, Francis L, Shugart YY, Strickland PT, Kao WH, Alani RM, Smith MW, Alberg AJ. A community-based study of nucleotide excision repair polymorphisms in relation to the risk of non-melanoma skin cancer. The Journal of Investigative Dermatology. 132: 1354-62. PMID 22336945 DOI: 10.1038/Jid.2012.4 |
0.386 |
|
2012 |
Saxena R, Elbers CC, Guo Y, Peter I, Gaunt TR, Mega JL, Lanktree MB, Tare A, Castillo BA, Li YR, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight BF, ... ... Ruczinski I, et al. Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. American Journal of Human Genetics. 90: 410-25. PMID 22325160 DOI: 10.1016/J.Ajhg.2011.12.022 |
0.424 |
|
2012 |
Wu T, Fallin MD, Shi M, Ruczinski I, Liang KY, Hetmanski JB, Wang H, Ingersoll RG, Huang S, Ye X, Wu-Chou YH, Chen PK, Jabs EW, Shi B, Redett R, et al. Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate. Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 76-83. PMID 22241686 DOI: 10.1002/Bdra.22885 |
0.402 |
|
2012 |
Schwender H, Taub MA, Beaty TH, Marazita ML, Ruczinski I. Rapid testing of SNPs and gene-environment interactions in case-parent trio data based on exact analytic parameter estimation. Biometrics. 68: 766-73. PMID 22150644 DOI: 10.1111/J.1541-0420.2011.01713.X |
0.397 |
|
2012 |
Wheless LE, Kistner-Griffin E, Jorgensen TJ, Ruczinski I, Berthier-Schaad Y, Kessing B, Hoffman-Bolton J, Woodward L, Yao Y, Strickland PT, Kao WHL, Alani RM, Smith MW, Alberg AJ. Abstract 2639: A community-based study of nucleotide excision repair polymorphisms in relation to risk of non-melanoma skin cancer Cancer Research. 72: 2639-2639. DOI: 10.1158/1538-7445.Am2012-2639 |
0.386 |
|
2012 |
Ruczinski I, Jorgensen T, Shugart YY, Berthier-Schaad Y, Kessing B, Hoffman-Bolton J, Helzlsouer K, Kao WHL, Wheless L, Francis L, Alani R, Strickland P, Smith M, Alberg AJ. Abstract 2636: Nonmelanoma skin cancer as a marker of a cancer-prone phenotype: Potential role of DNA repair gene variants Cancer Research. 72: 2636-2636. DOI: 10.1158/1538-7445.Am2012-2636 |
0.375 |
|
2011 |
Bhatia G, Patterson N, Pasaniuc B, Zaitlen N, Genovese G, Pollack S, Mallick S, Myers S, Tandon A, Spencer C, Palmer CD, Adeyemo AA, Akylbekova EL, Cupples LA, Divers J, ... ... Ruczinski I, et al. Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. American Journal of Human Genetics. 89: 368-81. PMID 21907010 DOI: 10.1016/J.Ajhg.2011.07.025 |
0.357 |
|
2011 |
Torgerson DG, Ampleford EJ, Chiu GY, Gauderman WJ, Gignoux CR, Graves PE, Himes BE, Levin AM, Mathias RA, Hancock DB, Baurley JW, Eng C, Stern DA, Celedón JC, Rafaels N, ... ... Ruczinski I, et al. Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations. Nature Genetics. 43: 887-92. PMID 21804549 DOI: 10.1038/Ng.888 |
0.376 |
|
2011 |
Faraday N, Yanek LR, Yang XP, Mathias R, Herrera-Galeano JE, Suktitipat B, Qayyum R, Johnson AD, Chen MH, Tofler GH, Ruczinski I, Friedman AD, Gylfason A, Thorsteinsdottir U, Bray PF, et al. Identification of a specific intronic PEAR1 gene variant associated with greater platelet aggregability and protein expression. Blood. 118: 3367-75. PMID 21791418 DOI: 10.1182/Blood-2010-11-320788 |
0.369 |
|
2011 |
Wegmann D, Kessner DE, Veeramah KR, Mathias RA, Nicolae DL, Yanek LR, Sun YV, Torgerson DG, Rafaels N, Mosley T, Becker LC, Ruczinski I, Beaty TH, Kardia SL, Meyers DA, et al. Recombination rates in admixed individuals identified by ancestry-based inference. Nature Genetics. 43: 847-53. PMID 21775992 DOI: 10.1038/Ng.894 |
0.309 |
|
2011 |
Beaty TH, Ruczinski I, Murray JC, Marazita ML, Munger RG, Hetmanski JB, Murray T, Redett RJ, Fallin MD, Liang KY, Wu T, Patel PJ, Jin SC, Zhang TX, Schwender H, et al. Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. Genetic Epidemiology. 35: 469-78. PMID 21618603 DOI: 10.1002/Gepi.20595 |
0.406 |
|
2011 |
Mathias RA, Sergeant S, Ruczinski I, Torgerson DG, Hugenschmidt CE, Kubala M, Vaidya D, Suktitipat B, Ziegler JT, Ivester P, Case D, Yanek LR, Freedman BI, Rudock ME, Barnes KC, et al. The impact of FADS genetic variants on ω6 polyunsaturated fatty acid metabolism in African Americans. Bmc Genetics. 12: 50. PMID 21599946 DOI: 10.1186/1471-2156-12-50 |
0.363 |
|
2011 |
Pasaniuc B, Zaitlen N, Lettre G, Chen GK, Tandon A, Kao WH, Ruczinski I, Fornage M, Siscovick DS, Zhu X, Larkin E, Lange LA, Cupples LA, Yang Q, Akylbekova EL, et al. Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium. Plos Genetics. 7: e1001371. PMID 21541012 DOI: 10.1371/Journal.Pgen.1001371 |
0.396 |
|
2011 |
Halper-Stromberg E, Frelin L, Ruczinski I, Scharpf R, Jie C, Carvalho B, Hao H, Hetrick K, Jedlicka A, Dziedzic A, Doheny K, Scott AF, Baylin S, Pevsner J, Spencer F, et al. Performance assessment of copy number microarray platforms using a spike-in experiment. Bioinformatics (Oxford, England). 27: 1052-60. PMID 21478196 DOI: 10.1093/Bioinformatics/Btr106 |
0.366 |
|
2011 |
Kral BG, Mathias RA, Suktitipat B, Ruczinski I, Vaidya D, Yanek LR, Quyyumi AA, Patel RS, Zafari AM, Vaccarino V, Hauser ER, Kraus WE, Becker LC, Becker DM. A common variant in the CDKN2B gene on chromosome 9p21 protects against coronary artery disease in Americans of African ancestry. Journal of Human Genetics. 56: 224-9. PMID 21270820 DOI: 10.1038/Jhg.2010.171 |
0.417 |
|
2011 |
Schwender H, Bowers K, Fallin MD, Ruczinski I. Importance measures for epistatic interactions in case-parent trios. Annals of Human Genetics. 75: 122-32. PMID 21118192 DOI: 10.1111/J.1469-1809.2010.00623.X |
0.341 |
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2011 |
Scharpf RB, Ruczinski I, Carvalho B, Doan B, Chakravarti A, Irizarry RA. A multilevel model to address batch effects in copy number estimation using SNP arrays. Biostatistics (Oxford, England). 12: 33-50. PMID 20625178 DOI: 10.1093/Biostatistics/Kxq043 |
0.381 |
|
2011 |
Schwender H, Ruczinski I, Ickstadt K. Testing SNPs and sets of SNPs for importance in association studies. Biostatistics (Oxford, England). 12: 18-32. PMID 20601626 DOI: 10.1093/Biostatistics/Kxq042 |
0.403 |
|
2011 |
Scharpf RB, Irizarry RA, Ritchie ME, Carvalho B, Ruczinski I. Using the R Package crlmm for Genotyping and Copy Number Estimation. Journal of Statistical Software. 40: 1-32. DOI: 10.18637/Jss.V040.I12 |
0.333 |
|
2010 |
Schwender H, Ruczinski I. Logic regression and its extensions. Advances in Genetics. 72: 25-45. PMID 21029847 DOI: 10.1016/B978-0-12-380862-2.00002-3 |
0.312 |
|
2010 |
Assimes TL, Hólm H, Kathiresan S, Reilly MP, Thorleifsson G, Voight BF, Erdmann J, Willenborg C, Vaidya D, Xie C, Patterson CC, Morgan TM, Burnett MS, Li M, Hlatky MA, ... ... Ruczinski I, et al. Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. Journal of the American College of Cardiology. 56: 1552-63. PMID 20933357 DOI: 10.1016/J.Jacc.2010.06.022 |
0.385 |
|
2010 |
Murray T, Beaty TH, Mathias RA, Rafaels N, Grant AV, Faruque MU, Watson HR, Ruczinski I, Dunston GM, Barnes KC. African and non-African admixture components in African Americans and an African Caribbean population. Genetic Epidemiology. 34: 561-8. PMID 20717976 DOI: 10.1002/Gepi.20512 |
0.359 |
|
2010 |
Wu T, Liang KY, Hetmanski JB, Ruczinski I, Fallin MD, Ingersoll RG, Wang H, Huang S, Ye X, Wu-Chou YH, Chen PK, Jabs EW, Shi B, Redett R, Scott AF, et al. Evidence of gene-environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate. Human Genetics. 128: 401-10. PMID 20652317 DOI: 10.1007/S00439-010-0863-Y |
0.412 |
|
2010 |
Li Q, Fallin MD, Louis TA, Lasseter VK, McGrath JA, Avramopoulos D, Wolyniec PS, Valle D, Liang KY, Pulver AE, Ruczinski I. Detection of SNP-SNP interactions in trios of parents with schizophrenic children. Genetic Epidemiology. 34: 396-406. PMID 20568257 DOI: 10.1002/Gepi.20488 |
0.384 |
|
2010 |
Hunninghake GM, Soto-Quirós ME, Avila L, Kim HP, Lasky-Su J, Rafaels N, Ruczinski I, Beaty TH, Mathias RA, Barnes KC, Wilk JB, O'Connor GT, Gauderman WJ, Vora H, Baurley JW, et al. TSLP polymorphisms are associated with asthma in a sex-specific fashion. Allergy. 65: 1566-75. PMID 20560908 DOI: 10.1111/J.1398-9995.2010.02415.X |
0.357 |
|
2010 |
Mathias RA, Kim Y, Sung H, Yanek LR, Mantese VJ, Hererra-Galeano JE, Ruczinski I, Wilson AF, Faraday N, Becker LC, Becker DM. A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease. Bmc Medical Genomics. 3: 22. PMID 20529293 DOI: 10.1186/1755-8794-3-22 |
0.327 |
|
2010 |
Beaty TH, Murray JC, Marazita ML, Munger RG, Ruczinski I, Hetmanski JB, Liang KY, Wu T, Murray T, Fallin MD, Redett RA, Raymond G, Schwender H, Jin SC, Cooper ME, et al. A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nature Genetics. 42: 525-9. PMID 20436469 DOI: 10.1038/Ng.580 |
0.445 |
|
2010 |
Louis TA, Ruczinski I. Efficient evaluation of ranking procedures when the number of units is large, with application to SNP identification. Biometrical Journal. Biometrische Zeitschrift. 52: 34-49. PMID 20131327 DOI: 10.1002/Bimj.200900044 |
0.357 |
|
2010 |
Sleiman PM, Flory J, Imielinski M, Bradfield JP, Annaiah K, Willis-Owen SA, Wang K, Rafaels NM, Michel S, Bonnelykke K, Zhang H, Kim CE, Frackelton EC, Glessner JT, Hou C, ... ... Ruczinski I, et al. Variants of DENND1B associated with asthma in children. The New England Journal of Medicine. 362: 36-44. PMID 20032318 DOI: 10.1056/Nejmoa0901867 |
0.375 |
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2010 |
Mathias RA, Grant AV, Rafaels N, Hand T, Gao L, Vergara C, Tsai YJ, Yang M, Campbell M, Foster C, Gao P, Togias A, Hansel NN, Diette G, Adkinson NF, ... ... Ruczinski I, et al. A genome-wide association study on African-ancestry populations for asthma. The Journal of Allergy and Clinical Immunology. 125: 336-346.e4. PMID 19910028 DOI: 10.1016/J.Jaci.2009.08.031 |
0.429 |
|
2009 |
Gallicchio L, Chang HH, Christo DK, Thuita L, Huang HY, Strickland P, Ruczinski I, Clipp S, Helzlsouer KJ. Single nucleotide polymorphisms in obesity-related genes and all-cause and cause-specific mortality: a prospective cohort study. Bmc Medical Genetics. 10: 103. PMID 19818126 DOI: 10.1186/1471-2350-10-103 |
0.33 |
|
2009 |
Jorgensen TJ, Ruczinski I, Kessing B, Smith MW, Shugart YY, Alberg AJ. Hypothesis-driven candidate gene association studies: practical design and analytical considerations. American Journal of Epidemiology. 170: 986-93. PMID 19762372 DOI: 10.1093/Aje/Kwp242 |
0.373 |
|
2009 |
Price AL, Tandon A, Patterson N, Barnes KC, Rafaels N, Ruczinski I, Beaty TH, Mathias R, Reich D, Myers S. Sensitive detection of chromosomal segments of distinct ancestry in admixed populations. Plos Genetics. 5: e1000519. PMID 19543370 DOI: 10.1371/Journal.Pgen.1000519 |
0.34 |
|
2009 |
Miller CL, Murakami P, Ruczinski I, Ross RG, Sinkus M, Sullivan B, Leonard S. Two complex genotypes relevant to the kynurenine pathway and melanotropin function show association with schizophrenia and bipolar disorder. Schizophrenia Research. 113: 259-67. PMID 19502010 DOI: 10.1016/J.Schres.2009.05.014 |
0.328 |
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2009 |
Köttgen A, Glazer NL, Dehghan A, Hwang SJ, Katz R, Li M, Yang Q, Gudnason V, Launer LJ, Harris TB, Smith AV, Arking DE, Astor BC, Boerwinkle E, Ehret GB, ... Ruczinski I, et al. Multiple loci associated with indices of renal function and chronic kidney disease. Nature Genetics. 41: 712-7. PMID 19430482 DOI: 10.1038/Ng.377 |
0.337 |
|
2009 |
Himes BE, Hunninghake GM, Baurley JW, Rafaels NM, Sleiman P, Strachan DP, Wilk JB, Willis-Owen SA, Klanderman B, Lasky-Su J, Lazarus R, Murphy AJ, Soto-Quiros ME, Avila L, Beaty T, ... ... Ruczinski I, et al. Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. American Journal of Human Genetics. 84: 581-93. PMID 19426955 DOI: 10.1016/J.Ajhg.2009.04.006 |
0.392 |
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2009 |
Lam TK, Ruczinski I, Helzlsouer K, Shugart YY, Li KE, Clipp S, Strickland PT, Alberg AJ. Copy number variants of GSTM1 and GSTT1 in relation to lung cancer risk in a prospective cohort study. Annals of Epidemiology. 19: 546-52. PMID 19394866 DOI: 10.1016/J.Annepidem.2009.03.003 |
0.317 |
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2009 |
Tsai YJ, Mathias R, Grant A, Rafaels N, Hand T, Togias A, Hansel N, Diette G, Adkinson NF, Liu MC, Faruque M, Watson H, Scott A, Ruczinski I, Dunston G, et al. AbstractSunday March 15A Genome Wide Approach to Identify Genetic Determinants of Asthma Traits Related to Airway Function in Two Populations of African Descent The Journal of Allergy and Clinical Immunology. 123. DOI: 10.1016/J.Jaci.2008.12.555 |
0.335 |
|
2008 |
Scharpf RB, Parmigiani G, Pevsner J, Ruczinski I. Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays. The Annals of Applied Statistics. 2: 687-713. PMID 19609370 DOI: 10.1214/07-Aoas155 |
0.379 |
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2008 |
Pattaro C, Ruczinski I, Fallin DM, Parmigiani G. Haplotype block partitioning as a tool for dimensionality reduction in SNP association studies. Bmc Genomics. 9: 405. PMID 18759977 DOI: 10.1186/1471-2164-9-405 |
0.421 |
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2008 |
Sull JW, Liang KY, Hetmanski JB, Fallin MD, Ingersoll RG, Park J, Wu-Chou YH, Chen PK, Chong SS, Cheah F, Yeow V, Park BY, Jee SH, Jabs EW, Redett R, ... ... Ruczinski I, et al. Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations. Genetic Epidemiology. 32: 505-12. PMID 18357615 DOI: 10.1002/Gepi.20323 |
0.368 |
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2008 |
Gallicchio L, Chang H, Christo DK, Thuita L, Huang HY, Strickland P, Ruczinski I, Hoffman SC, Helzlsouer KJ. Single nucleotide polymorphisms in inflammation-related genes and mortality in a community-based cohort in Washington County, Maryland. American Journal of Epidemiology. 167: 807-13. PMID 18263601 DOI: 10.1093/Aje/Kwm378 |
0.384 |
|
2008 |
Tsai YJ, Mathias R, Grant A, Rafaels N, Hand T, Togias A, Hansel N, Diette G, Adkinson NF, Liu MC, Faruque M, Watson H, Scott A, Ruczinski I, Dunston G, et al. A Genome Wide Approach to Identify Genetic Determinants of Asthma Traits Related to Airway Function in Populations of African Descent The Journal of Allergy and Clinical Immunology. 121. DOI: 10.1016/J.Jaci.2007.12.258 |
0.349 |
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2007 |
Ting JC, Roberson ED, Miller ND, Lysholm-Bernacchi A, Stephan DA, Capone GT, Ruczinski I, Thomas GH, Pevsner J. Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio. Human Mutation. 28: 1225-35. PMID 17661425 DOI: 10.1002/Humu.20583 |
0.365 |
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2007 |
Scharpf RB, Ting JC, Pevsner J, Ruczinski I. SNPchip: R classes and methods for SNP array data. Bioinformatics (Oxford, England). 23: 627-8. PMID 17204461 DOI: 10.1093/Bioinformatics/Btl638 |
0.372 |
|
2007 |
Jorgensen TJ, Visvanathan K, Ruczinski I, Thuita L, Hoffman S, Helzlsouer KJ. Breast cancer risk is not associated with polymorphic forms of xeroderma pigmentosum genes in a cohort of women from Washington County, Maryland Breast Cancer Research and Treatment. 101: 65-71. PMID 16823510 DOI: 10.1007/S10549-006-9263-3 |
0.357 |
|
2006 |
Dai JY, Ruczinski I, LeBlanc M, Kooperberg C. Imputation methods to improve inference in SNP association studies. Genetic Epidemiology. 30: 690-702. PMID 16986162 DOI: 10.1002/Gepi.20180 |
0.375 |
|
2006 |
Brown EE, Fallin D, Ruczinski I, Hutchinson A, Staats B, Vitale F, Lauria C, Serraino D, Rezza G, Mbisa G, Whitby D, Messina A, Goedert JJ, Chanock SJ. Associations of classic Kaposi sarcoma with common variants in genes that modulate host immunity. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 15: 926-34. PMID 16702372 DOI: 10.1158/1055-9965.Epi-05-0791 |
0.343 |
|
2006 |
Ting JC, Ye Y, Thomas GH, Ruczinski I, Pevsner J. Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan. Bmc Bioinformatics. 7: 25. PMID 16420694 DOI: 10.1186/1471-2105-7-25 |
0.383 |
|
2006 |
Brewster AM, Jorgensen TJ, Ruczinski I, Huang HY, Hoffman S, Thuita L, Newschaffer C, Lunn RM, Bell D, Helzlsouer KJ. Polymorphisms of the DNA repair genes XPD (Lys751Gln) and XRCC1 (Arg399Gln and Arg194Trp): Relationship to breast cancer risk and familial predisposition to breast cancer Breast Cancer Research and Treatment. 95: 73-80. PMID 16319991 DOI: 10.1007/S10549-005-9045-3 |
0.337 |
|
2005 |
Kooperberg C, Ruczinski I. Identifying interacting SNPs using Monte Carlo logic regression Genetic Epidemiology. 28: 157-170. PMID 15532037 DOI: 10.1002/Gepi.20042 |
0.389 |
|
2001 |
Kooperberg C, Ruczinski I, Leblanc ML, Hsu L. Sequence analysis using logic regression Genetic Epidemiology. 21. PMID 11793751 DOI: 10.1002/Gepi.2001.21.S1.S626 |
0.393 |
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