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The publication data currently available has been vetted by Vanderbilt faculty, staff, administrators and trainees. The data itself is retrieved directly from NCBI's PubMed and is automatically updated on a weekly basis to ensure accuracy and completeness.

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Results: 1 to 10 of 38

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Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population.
Zanetti KA, Wang Z, Aldrich M, Amos CI, Blot WJ, Bowman ED, Burdette L, Cai Q, Caporaso N, Chung CC, Gillanders EM, Haiman CA, Hansen HM, Henderson BE, Kolonel LN, Marchand LL, Li S, McNeill LH, Ryan BM, Schwartz AG, Sison JD, Spitz MR, Tucker M, Wenzlaff AS, Wiencke JK, Wilkens L, Wrensch MR, Wu X, Zheng W, Zhou W, Christiani D, Palmer JR, Penning TM, Rieber AG, Rosenberg L, Ruiz-Narvaez EA, Su L, Vachani A, Wei Y, Whitehead AS, Chanock SJ, Harris CC
(2016) Lung Cancer 98: 33-42
MeSH Terms: African Americans, Case-Control Studies, Chromosomes, Human, Pair 15, Chromosomes, Human, Pair 5, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Lung Neoplasms, Polymorphism, Single Nucleotide, Population Surveillance, Quantitative Trait Loci
Added April 3, 2018
0 Communities
1 Members
0 Resources
MeSH Terms
Admixture mapping identifies a locus at 15q21.2-22.3 associated with keloid formation in African Americans.
Velez Edwards DR, Tsosie KS, Williams SM, Edwards TL, Russell SB
(2014) Hum Genet 133: 1513-23
MeSH Terms: African Americans, Case-Control Studies, Chromosome Mapping, Chromosomes, Human, Pair 15, Exome, Female, Gene Frequency, Genetic Association Studies, Genetic Loci, Genetic Predisposition to Disease, Humans, Keloid, Male, Polymorphism, Single Nucleotide
Added February 12, 2015
0 Communities
1 Members
0 Resources
14 MeSH Terms
Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1.
Cai Q, Zhang B, Sung H, Low SK, Kweon SS, Lu W, Shi J, Long J, Wen W, Choi JY, Noh DY, Shen CY, Matsuo K, Teo SH, Kim MK, Khoo US, Iwasaki M, Hartman M, Takahashi A, Ashikawa K, Matsuda K, Shin MH, Park MH, Zheng Y, Xiang YB, Ji BT, Park SK, Wu PE, Hsiung CN, Ito H, Kasuga Y, Kang P, Mariapun S, Ahn SH, Kang HS, Chan KY, Man EP, Iwata H, Tsugane S, Miao H, Liao J, Nakamura Y, Kubo M, DRIVE GAME-ON Consortium, Delahanty RJ, Zhang Y, Li B, Li C, Gao YT, Shu XO, Kang D, Zheng W
(2014) Nat Genet 46: 886-90
MeSH Terms: Adult, Asians, Breast Neoplasms, Case-Control Studies, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 15, Chromosomes, Human, Pair 5, Far East, Female, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Middle Aged, Risk, Whites
Added January 23, 2015
0 Communities
3 Members
0 Resources
16 MeSH Terms
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia.
Lan Q, Hsiung CA, Matsuo K, Hong YC, Seow A, Wang Z, Hosgood HD, Chen K, Wang JC, Chatterjee N, Hu W, Wong MP, Zheng W, Caporaso N, Park JY, Chen CJ, Kim YH, Kim YT, Landi MT, Shen H, Lawrence C, Burdett L, Yeager M, Yuenger J, Jacobs KB, Chang IS, Mitsudomi T, Kim HN, Chang GC, Bassig BA, Tucker M, Wei F, Yin Z, Wu C, An SJ, Qian B, Lee VH, Lu D, Liu J, Jeon HS, Hsiao CF, Sung JS, Kim JH, Gao YT, Tsai YH, Jung YJ, Guo H, Hu Z, Hutchinson A, Wang WC, Klein R, Chung CC, Oh IJ, Chen KY, Berndt SI, He X, Wu W, Chang J, Zhang XC, Huang MS, Zheng H, Wang J, Zhao X, Li Y, Choi JE, Su WC, Park KH, Sung SW, Shu XO, Chen YM, Liu L, Kang CH, Hu L, Chen CH, Pao W, Kim YC, Yang TY, Xu J, Guan P, Tan W, Su J, Wang CL, Li H, Sihoe AD, Zhao Z, Chen Y, Choi YY, Hung JY, Kim JS, Yoon HI, Cai Q, Lin CC, Park IK, Xu P, Dong J, Kim C, He Q, Perng RP, Kohno T, Kweon SS, Chen CY, Vermeulen R, Wu J, Lim WY, Chen KC, Chow WH, Ji BT, Chan JK, Chu M, Li YJ, Yokota J, Li J, Chen H, Xiang YB, Yu CJ, Kunitoh H, Wu G, Jin L, Lo YL, Shiraishi K, Chen YH, Lin HC, Wu T, Wu YL, Yang PC, Zhou B, Shin MH, Fraumeni JF, Lin D, Chanock SJ, Rothman N
(2012) Nat Genet 44: 1330-5
MeSH Terms: Adenocarcinoma, Adenocarcinoma of Lung, Adult, Aged, Asians, Carcinoma, Squamous Cell, Chromosomes, Human, Pair 10, Chromosomes, Human, Pair 15, Chromosomes, Human, Pair 17, Chromosomes, Human, Pair 5, Chromosomes, Human, Pair 6, Female, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Lung Neoplasms, Middle Aged, Polymorphism, Single Nucleotide, Smoking
Added September 3, 2013
0 Communities
3 Members
0 Resources
20 MeSH Terms
Genome-wide meta-analyses of smoking behaviors in African Americans.
David SP, Hamidovic A, Chen GK, Bergen AW, Wessel J, Kasberger JL, Brown WM, Petruzella S, Thacker EL, Kim Y, Nalls MA, Tranah GJ, Sung YJ, Ambrosone CB, Arnett D, Bandera EV, Becker DM, Becker L, Berndt SI, Bernstein L, Blot WJ, Broeckel U, Buxbaum SG, Caporaso N, Casey G, Chanock SJ, Deming SL, Diver WR, Eaton CB, Evans DS, Evans MK, Fornage M, Franceschini N, Harris TB, Henderson BE, Hernandez DG, Hitsman B, Hu JJ, Hunt SC, Ingles SA, John EM, Kittles R, Kolb S, Kolonel LN, Le Marchand L, Liu Y, Lohman KK, McKnight B, Millikan RC, Murphy A, Neslund-Dudas C, Nyante S, Press M, Psaty BM, Rao DC, Redline S, Rodriguez-Gil JL, Rybicki BA, Signorello LB, Singleton AB, Smoller J, Snively B, Spring B, Stanford JL, Strom SS, Swan GE, Taylor KD, Thun MJ, Wilson AF, Witte JS, Yamamura Y, Yanek LR, Yu K, Zheng W, Ziegler RG, Zonderman AB, Jorgenson E, Haiman CA, Furberg H
(2012) Transl Psychiatry 2: e119
MeSH Terms: Adult, African Americans, Aged, Chromosomes, Human, Pair 10, Chromosomes, Human, Pair 15, Female, Genetic Loci, Genetic Predisposition to Disease, Genetic Variation, Genome-Wide Association Study, Genotype, Humans, Male, Middle Aged, Nerve Tissue Proteins, Phenotype, Polymorphism, Single Nucleotide, Proteoglycans, Receptors, Nicotinic, Smoking, Statistics as Topic
Added March 20, 2014
0 Communities
1 Members
0 Resources
21 MeSH Terms
Reconstructability analysis as a tool for identifying gene-gene interactions in studies of human diseases.
Shervais S, Kramer PL, Westaway SK, Cox NJ, Zwick M
(2010) Stat Appl Genet Mol Biol 9: Article18
MeSH Terms: Algorithms, Bayes Theorem, Biostatistics, Case-Control Studies, Chromosomes, Human, Pair 15, Chromosomes, Human, Pair 2, Computer Simulation, Databases, Genetic, Diabetes Mellitus, Type 2, Disease, Epistasis, Genetic, Genes, Genomics, Humans, Inheritance Patterns, Linear Models, Logistic Models, Models, Genetic, Models, Statistical, Penetrance, Polymorphism, Single Nucleotide
Added February 22, 2016
0 Communities
1 Members
0 Resources
21 MeSH Terms
Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism.
Delahanty RJ, Kang JQ, Brune CW, Kistner EO, Courchesne E, Cox NJ, Cook EH, Macdonald RL, Sutcliffe JS
(2011) Mol Psychiatry 16: 86-96
MeSH Terms: Autistic Disorder, Chromosomes, Human, Pair 15, Female, Genome-Wide Association Study, Germ-Line Mutation, Humans, Male, Pedigree, Polymorphism, Single Nucleotide, Receptors, GABA-A
Added February 20, 2014
0 Communities
2 Members
0 Resources
10 MeSH Terms
Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.
Liu XQ, Paterson AD, Szatmari P, Autism Genome Project Consortium
(2008) Biol Psychiatry 64: 561-70
MeSH Terms: Autistic Disorder, Child, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 15, Female, Genetic Linkage, Genetic Markers, Genome-Wide Association Study, Humans, Interpersonal Relations, Male, Phenotype, Verbal Behavior
Added February 20, 2014
0 Communities
1 Members
0 Resources
13 MeSH Terms
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
Kim SJ, Brune CW, Kistner EO, Christian SL, Courchesne EH, Cox NJ, Cook EH
(2008) Am J Med Genet B Neuropsychiatr Genet 147B: 1116-25
MeSH Terms: Autistic Disorder, Child, Child, Preschool, Chromosomes, Human, Pair 15, Female, Gene Regulatory Networks, Genetic Predisposition to Disease, Genomic Imprinting, Genotype, Humans, Linkage Disequilibrium, Male, Phenotype, Polymorphism, Single Nucleotide, Receptors, GABA-A, Serotonin Plasma Membrane Transport Proteins
Added February 22, 2016
0 Communities
1 Members
0 Resources
16 MeSH Terms
Genetic studies of stuttering in a founder population.
Wittke-Thompson JK, Ambrose N, Yairi E, Roe C, Cook EH, Ober C, Cox NJ
(2007) J Fluency Disord 32: 33-50
MeSH Terms: Child, Chromosomes, Human, Pair 13, Chromosomes, Human, Pair 15, Chromosomes, Human, Pair 3, Genetic Linkage, Genotype, Humans, Pedigree, Population Surveillance, Stuttering
Added February 22, 2016
0 Communities
1 Members
0 Resources
10 MeSH Terms