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Items: 1 to 20 of 307


Rs12970134 near MC4R is associated with appetite and beverage intake in overweight and obese children: A family-based association study in Chinese population.

Wang S, Song J, Yang Y, Chawla NV, Ma J, Wang H.

PLoS One. 2017 May 16;12(5):e0177983. doi: 10.1371/journal.pone.0177983. eCollection 2017.


On the association analysis of CNV data: a fast and robust family-based association method.

Liu M, Moon S, Wang L, Kim S, Kim YJ, Hwang MY, Kim YJ, Elston RC, Kim BJ, Won S.

BMC Bioinformatics. 2017 Apr 18;18(1):217. doi: 10.1186/s12859-017-1622-z.


Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD).

Ritter ML, Guo W, Samuels JF, Wang Y, Nestadt PS, Krasnow J, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Murphy DL, Knowles JA, Grados MA, Riddle MA, Rasmussen SA, McLaughlin NC, Nurmi EL, Askland KD, Cullen B, Piacentini J, Pauls DL, Bienvenu J, Stewart E, Goes FS, Maher B, Pulver AE, Mattheisen M, Qian J, Nestadt G, Shugart YY.

Front Mol Neurosci. 2017 Mar 23;10:83. doi: 10.3389/fnmol.2017.00083. eCollection 2017.


The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.

He Z, Zhang D, Renton AE, Li B, Zhao L, Wang GT, Goate AM, Mayeux R, Leal SM.

Am J Hum Genet. 2017 Feb 2;100(2):193-204. doi: 10.1016/j.ajhg.2016.12.001. Epub 2017 Jan 5. Erratum in: Am J Hum Genet. 2017 Feb 2;100(2):371.


Comparing family-based rare variant association tests for dichotomous phenotypes.

Wang L, Choi S, Lee S, Park T, Won S.

BMC Proc. 2016 Oct 18;10(Suppl 7):181-186. eCollection 2016.


Fast Genome-Wide QTL Association Mapping on Pedigree and Population Data.

Zhou H, Blangero J, Dyer TD, Chan KK, Lange K, Sobel EM.

Genet Epidemiol. 2017 Apr;41(3):174-186. doi: 10.1002/gepi.21988. Epub 2016 Dec 12.


ASD and Genetic Associations with Receptors for Oxytocin and Vasopressin-AVPR1A, AVPR1B, and OXTR.

Francis SM, Kim SJ, Kistner-Griffin E, Guter S, Cook EH, Jacob S.

Front Neurosci. 2016 Nov 22;10:516. eCollection 2016.


Associations between homocysteine metabolism related SNPs and carotid intima-media thickness: a Chinese sib pair study.

Sun K, Song J, Liu K, Fang K, Wang L, Wang X, Li J, Tang X, Wu Y, Qin X, Wu T, Gao P, Chen D, Hu Y.

J Thromb Thrombolysis. 2017 Apr;43(3):401-410. doi: 10.1007/s11239-016-1449-x.


CERAMIC: Case-Control Association Testing in Samples with Related Individuals, Based on Retrospective Mixed Model Analysis with Adjustment for Covariates.

Zhong S, Jiang D, McPeek MS.

PLoS Genet. 2016 Oct 3;12(10):e1006329. doi: 10.1371/journal.pgen.1006329. eCollection 2016 Oct.


Family-Based Rare Variant Association Analysis: A Fast and Efficient Method of Multivariate Phenotype Association Analysis.

Wang L, Lee S, Gim J, Qiao D, Cho M, Elston RC, Silverman EK, Won S.

Genet Epidemiol. 2016 Sep;40(6):502-11. doi: 10.1002/gepi.21985. Epub 2016 Jun 17.


Variants in Adjacent Oxytocin/Vasopressin Gene Region and Associations with ASD Diagnosis and Other Autism Related Endophenotypes.

Francis SM, Kistner-Griffin E, Yan Z, Guter S, Cook EH, Jacob S.

Front Neurosci. 2016 May 12;10:195. doi: 10.3389/fnins.2016.00195. eCollection 2016.


Using Incomplete Trios to Boost Confidence in Family Based Association Studies.

Dhankani V, Gibbs DL, Knijnenburg T, Kramer R, Vockley J, Niederhuber J, Shmulevich I, Bernard B.

Front Genet. 2016 Mar 18;7:34. doi: 10.3389/fgene.2016.00034. eCollection 2016.


TNFSF10/TRAIL regulates human T4 effector memory lymphocyte radiosensitivity and predicts radiation-induced acute and subacute dermatitis.

Baijer J, Déchamps N, Perdry H, Morales P, Kerns S, Vasilescu A, Baulande S, Azria D, Roméo PH, Schmitz A.

Oncotarget. 2016 Apr 19;7(16):21416-27. doi: 10.18632/oncotarget.7893.


Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3.

Herold C, Hooli BV, Mullin K, Liu T, Roehr JT, Mattheisen M, Parrado AR, Bertram L, Lange C, Tanzi RE.

Mol Psychiatry. 2016 Nov;21(11):1608-1612. doi: 10.1038/mp.2015.218. Epub 2016 Feb 2.


Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes.

Ge Y, Onengut-Gumuscu S, Quinlan AR, Mackey AJ, Wright JA, Buckner JH, Habib T, Rich SS, Concannon P.

Diabetes. 2016 Mar;65(3):794-802. doi: 10.2337/db15-0322. Epub 2015 Dec 2.


Association of IL10 Polymorphisms and Leprosy: A Meta-Analysis.

Alvarado-Arnez LE, Amaral EP, Sales-Marques C, Durães SM, Cardoso CC, Nunes Sarno E, Pacheco AG, Lana FC, Moraes MO.

PLoS One. 2015 Sep 4;10(9):e0136282. doi: 10.1371/journal.pone.0136282. eCollection 2015.


A New Role for LOC101928437 in Non-Syndromic Intellectual Disability: Findings from a Family-Based Association Test.

Zhou S, Shi Z, Cui M, Li J, Ma Z, Shi Y, Zheng Z, Zhang F, Jin T, Geng T, Chen C, Guo Y, Zhou J, Huang S, Guo X, Gao L, Gong P, Gao X, Zhang K.

PLoS One. 2015 Aug 19;10(8):e0135669. doi: 10.1371/journal.pone.0135669. eCollection 2015.


Adjusting heterogeneous ascertainment bias for genetic association analysis with extended families.

Park S, Lee S, Lee Y, Herold C, Hooli B, Mullin K, Park T, Park C, Bertram L, Lange C, Tanzi R, Won S.

BMC Med Genet. 2015 Aug 19;16:62. doi: 10.1186/s12881-015-0198-6.


Sequencing of the TBX6 Gene in Families with Familial Idiopathic Scoliosis.

Baschal EE, Swindle K, Justice CM, Baschal RM, Perera A, Wethey CI, Poole A, Pourquié O, Tassy O, Miller NH.

Spine Deform. 2015 Jul;3(4):288-296.

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