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Results: 1 to 10 of 21

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A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolton PF, Bourgeron T, Brennan S, Cali P, Correia C, Corsello C, Coutanche M, Dawson G, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Foley S, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Green J, Guter SJ, Hakonarson H, Holt R, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Lamb JA, Leboyer M, Le Couteur A, Leventhal BL, Lord C, Lund SC, Maestrini E, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Miller J, Minopoli F, Mirza GK, Munson J, Nelson SF, Nygren G, Oliveira G, Pagnamenta AT, Papanikolaou K, Parr JR, Parrini B, Pickles A, Pinto D, Piven J, Posey DJ, Poustka A, Poustka F, Ragoussis J, Roge B, Rutter ML, Sequeira AF, Soorya L, Sousa I, Sykes N, Stoppioni V, Tancredi R, Tauber M, Thompson AP, Thomson S, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Vorstman JA, Wallace S, Wang K, Wassink TH, White K, Wing K, Wittemeyer K, Yaspan BL, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Geschwind DH, Haines JL, Hallmayer J, Monaco AP, Nurnberger JI, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vieland VJ, Wijsman EM, Green A, Gill M, Gallagher L, Vicente A, Ennis S
(2012) Hum Genet 131: 565-79
MeSH Terms: Adult, Child, Child Development Disorders, Pervasive, Cluster Analysis, Cohort Studies, DNA Copy Number Variations, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Haplotypes, Homozygote, Humans, Linkage Disequilibrium, Male, Middle Aged, Nuclear Family, Polymorphism, Single Nucleotide
Added February 20, 2014
0 Communities
1 Members
0 Resources
18 MeSH Terms
Diabetic subjects diagnosed through the Diabetes Prevention Trial-Type 1 (DPT-1) are often asymptomatic with normal A1C at diabetes onset.
Triolo TM, Chase HP, Barker JM, DPT-1 Study Group
(2009) Diabetes Care 32: 769-73
MeSH Terms: Adolescent, Adult, Autoantibodies, Blood Glucose, Child, Diabetes Mellitus, Diabetes Mellitus, Type 1, Family, Female, Glucose Tolerance Test, Glycated Hemoglobin A, Humans, Islets of Langerhans, Male, Mass Screening, Middle Aged, Nuclear Family, Randomized Controlled Trials as Topic, Reference Values, Young Adult
Added March 29, 2019
0 Communities
1 Members
0 Resources
MeSH Terms
AHSG gene polymorphisms are associated with bone mineral density in Caucasian nuclear families.
Yang YJ, Wang YB, Lei SF, Long JR, Shen H, Zhao LJ, Jiang DK, Xiao SM, Chen XD, Chen Y, Deng HW
(2007) Eur J Epidemiol 22: 527-32
MeSH Terms: Adult, Blood Proteins, Bone Density, European Continental Ancestry Group, Female, Gene Frequency, Genetic Linkage, Haplotypes, Humans, Male, Middle Aged, Nebraska, Nuclear Family, Osteoporosis, Polymorphism, Genetic, alpha-2-HS-Glycoprotein
Added December 10, 2013
0 Communities
1 Members
0 Resources
16 MeSH Terms
Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism.
Cross S, Kim SJ, Weiss LA, Delahanty RJ, Sutcliffe JS, Leventhal BL, Cook EH, Veenstra-Vanderweele J
(2008) Neuropsychopharmacology 33: 353-60
MeSH Terms: Adult, African Continental Ancestry Group, Asian Continental Ancestry Group, Autistic Disorder, Blood Platelets, DNA Primers, European Continental Ancestry Group, Female, Hispanic Americans, Humans, Male, Nuclear Family, Platelet Count, Polymorphism, Genetic, Polymorphism, Single Nucleotide, Serotonin, Serotonin Plasma Membrane Transport Proteins
Added February 20, 2014
0 Communities
1 Members
0 Resources
17 MeSH Terms
Genetic determination of variation and covariation of bone mineral density at the hip and spine in a Chinese population.
Jian WX, Long JR, Li MX, Liu XH, Deng HW
(2005) J Bone Miner Metab 23: 181-5
MeSH Terms: Adult, Aged, Bone Density, China, Female, Genetic Variation, Hip, Humans, Male, Middle Aged, Nuclear Family, Siblings, Spine
Added December 10, 2013
0 Communities
1 Members
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13 MeSH Terms
Vitamin D receptor gene polymorphisms are linked to and associated with adult height.
Xiong DH, Xu FH, Liu PY, Shen H, Long JR, Elze L, Recker RR, Deng HW
(2005) J Med Genet 42: 228-34
MeSH Terms: Adult, Body Height, Female, Gene Frequency, Haplotypes, Humans, Linkage Disequilibrium, Male, Middle Aged, Nuclear Family, Polymorphism, Single Nucleotide, Receptors, Calcitriol
Added December 10, 2013
0 Communities
1 Members
0 Resources
12 MeSH Terms
Heritability of spinal trabecular volumetric bone mineral density measured by QCT in the Diabetes Heart Study.
Lenchik L, Hsu FC, Register TC, Lohman KK, Freedman BI, Langefeld CD, Bowden DW, Carr JJ
(2004) Calcif Tissue Int 75: 305-12
MeSH Terms: Absorptiometry, Photon, Adult, Aged, Aged, 80 and over, Bone Density, Diabetes Mellitus, Type 2, Female, Genetic Predisposition to Disease, Humans, Inheritance Patterns, Male, Middle Aged, Nuclear Family, Osteoporosis, Postmenopausal, Spine, Tomography, X-Ray Computed
Added February 15, 2014
0 Communities
1 Members
0 Resources
16 MeSH Terms
APOE haplotypes influence bone mineral density in Caucasian males but not females.
Long JR, Liu PY, Liu YJ, Lu Y, Shen H, Zhao LJ, Xiong DH, Deng HW
(2004) Calcif Tissue Int 75: 299-304
MeSH Terms: Absorptiometry, Photon, Adult, Apolipoproteins E, Bone Density, European Continental Ancestry Group, Female, Gene Frequency, Genetic Predisposition to Disease, Haplotypes, Humans, Linkage Disequilibrium, Lumbar Vertebrae, Male, Middle Aged, Nuclear Family, Osteoporosis, Polymorphism, Single Nucleotide, Premenopause, Sex Factors
Added December 10, 2013
0 Communities
1 Members
0 Resources
19 MeSH Terms
Living-related transplantation of an ectopic pelvic kidney.
Grogan EL, Nylander WA, Shaffer D
(2004) Transplantation 77: 953
MeSH Terms: Adult, Anastomosis, Surgical, Arterial Occlusive Diseases, Female, Hepatectomy, Hepatic Artery, Humans, Liver Transplantation, Living Donors, Mesenteric Arteries, Nuclear Family, Portal Vein
Added March 5, 2014
0 Communities
1 Members
0 Resources
12 MeSH Terms
Tests of linkage and/or association of the LEPR gene polymorphisms with obesity phenotypes in Caucasian nuclear families.
Liu YJ, Rocha-Sanchez SM, Liu PY, Long JR, Lu Y, Elze L, Recker RR, Deng HW
(2004) Physiol Genomics 17: 101-6
MeSH Terms: Adult, European Continental Ancestry Group, Female, Gene Frequency, Genetic Linkage, Haplotypes, Humans, Linkage Disequilibrium, Male, Middle Aged, Nuclear Family, Obesity, Phenotype, Polymorphism, Single Nucleotide, Receptors, Cell Surface, Receptors, Leptin
Added December 10, 2013
0 Communities
1 Members
0 Resources
16 MeSH Terms