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Items: 1 to 20 of 702

1.

Polymorphisms of STS gene and SULT2A1 gene and neurosteroid levels in Han Chinese boys with attention-deficit/hyperactivity disorder: an exploratory investigation.

Wang LJ, Chan WC, Chou MC, Chou WJ, Lee MJ, Lee SY, Lin PY, Yang YH, Yen CF.

Sci Rep. 2017 Apr 3;7:45595. doi: 10.1038/srep45595.

2.

Family-based association study of DRD4 gene in methylphenidate-responded Attention Deficit/Hyperactivity Disorder.

Leung PW, Chan JK, Chen LH, Lee CC, Hung SF, Ho TP, Tang CP, Moyzis RK, Swanson JM.

PLoS One. 2017 Mar 10;12(3):e0173748. doi: 10.1371/journal.pone.0173748. eCollection 2017.

3.

ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development.

Zhang R, Knapp M, Suzuki K, Kajioka D, Schmidt JM, Winkler J, Yilmaz Ö, Pleschka M, Cao J, Kockum CC, Barker G, Holmdahl G, Beaman G, Keene D, Woolf AS, Cervellione RM, Cheng W, Wilkins S, Gearhart JP, Sirchia F, Di Grazia M, Ebert AK, Rösch W, Ellinger J, Jenetzky E, Zwink N, Feitz WF, Marcelis C, Schumacher J, Martinón-Torres F, Hibberd ML, Khor CC, Heilmann-Heimbach S, Barth S, Boyadjiev SA, Brusco A, Ludwig M, Newman W, Nordenskjöld A, Yamada G, Odermatt B, Reutter H.

Sci Rep. 2017 Feb 8;7:42170. doi: 10.1038/srep42170.

4.

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.

PMID:
28065470
5.

Assessing transmission ratio distortion in extended families: a comparison of analysis methods.

Bhatnagar SR, Greenwood CM, Labbe A.

BMC Proc. 2016 Oct 18;10(Suppl 7):197-202. eCollection 2016.

6.

A Killer Immunoglobulin - Like Receptor Gene - Content Haplotype and A Cognate Human Leukocyte Antigen Ligand are Associated with Autism.

Torres A, Westover J, Benson M, Johnson R, Dykes A.

Autism Open Access. 2016 Apr;6(2). pii: 171. Epub 2016 Mar 28.

7.

Test for association of common variants in GRM7 with alcohol consumption.

Melroy-Greif WE, Vadasz C, Kamens HM, McQueen MB, Corley RP, Stallings MC, Hopfer CJ, Krauter KS, Brown SA, Hewitt JK, Ehringer MA.

Alcohol. 2016 Sep;55:43-50. doi: 10.1016/j.alcohol.2015.10.005. Epub 2016 Aug 31.

PMID:
27788777
8.

Analysis of Case-Parent Trios Using a Loglinear Model with Adjustment for Transmission Ratio Distortion.

Huang LO, Infante-Rivard C, Labbe A.

Front Genet. 2016 Aug 31;7:155. doi: 10.3389/fgene.2016.00155. eCollection 2016.

9.
10.

The impact of genotype calling errors on family-based studies.

Yan Q, Chen R, Sutcliffe JS, Cook EH, Weeks DE, Li B, Chen W.

Sci Rep. 2016 Jun 22;6:28323. doi: 10.1038/srep28323.

11.

Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples.

Yan Q, Weeks DE, Tiwari HK, Yi N, Zhang K, Gao G, Lin WY, Lou XY, Chen W, Liu N.

Hum Hered. 2015;80(3):126-38. doi: 10.1159/000445057. Epub 2016 Apr 29.

12.

A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies.

Bodea CA, Neale BM, Ripke S; International IBD Genetics Consortium., Daly MJ, Devlin B, Roeder K.

Am J Hum Genet. 2016 May 5;98(5):857-68. doi: 10.1016/j.ajhg.2016.02.025. Epub 2016 Apr 14.

13.

Testing Allele Transmission of an SNP Set Using a Family-Based Generalized Genetic Random Field Method.

Li M, Li J, He Z, Lu Q, Witte JS, Macleod SL, Hobbs CA, Cleves MA; National Birth Defects Prevention Study..

Genet Epidemiol. 2016 May;40(4):341-51. doi: 10.1002/gepi.21970. Epub 2016 Apr 7.

14.

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.

15.

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

Leslie EJ, Carlson JC, Shaffer JR, Feingold E, Wehby G, Laurie CA, Jain D, Laurie CC, Doheny KF, McHenry T, Resick J, Sanchez C, Jacobs J, Emanuele B, Vieira AR, Neiswanger K, Lidral AC, Valencia-Ramirez LC, Lopez-Palacio AM, Valencia DR, Arcos-Burgos M, Czeizel AE, Field LL, Padilla CD, Cutiongco-de la Paz EM, Deleyiannis F, Christensen K, Munger RG, Lie RT, Wilcox A, Romitti PA, Castilla EE, Mereb JC, Poletta FA, Orioli IM, Carvalho FM, Hecht JT, Blanton SH, Buxó CJ, Butali A, Mossey PA, Adeyemo WL, James O, Braimah RO, Aregbesola BS, Eshete MA, Abate F, Koruyucu M, Seymen F, Ma L, de Salamanca JE, Weinberg SM, Moreno L, Murray JC, Marazita ML.

Hum Mol Genet. 2016 Jul 1;25(13):2862-2872. Epub 2016 Mar 30.

PMID:
27033726
16.

Risk and resistance perspectives in translation-oriented etiology research.

Vanyukov MM, Tarter RE, Conway KP, Kirillova GP, Chandler RK, Daley DC.

Transl Behav Med. 2016 Mar;6(1):44-54. doi: 10.1007/s13142-015-0355-7. Review.

17.

Family-based approaches: design, imputation, analysis, and beyond.

Wijsman EM.

BMC Genet. 2016 Feb 3;17 Suppl 2:9. doi: 10.1186/s12863-015-0318-5.

18.

Analysis of Genes Involved in Body Weight Regulation by Targeted Re-Sequencing.

Volckmar AL, Han CT, Pütter C, Haas S, Vogel CI, Knoll N, Struve C, Göbel M, Haas K, Herrfurth N, Jarick I, Grallert H, Schürmann A, Al-Hasani H, Hebebrand J, Sauer S, Hinney A.

PLoS One. 2016 Feb 1;11(2):e0147904. doi: 10.1371/journal.pone.0147904. eCollection 2016.

19.

No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci.

Escott-Price V, Kirov G, Rees E, Isles AR, Owen MJ, O'Donovan MC.

PLoS One. 2015 Dec 3;10(12):e0144172. doi: 10.1371/journal.pone.0144172. eCollection 2015.

20.

The Norwegian preeclampsia family cohort study: a new resource for investigating genetic aspects and heritability of preeclampsia and related phenotypes.

Roten LT, Thomsen LC, Gundersen AS, Fenstad MH, Odland ML, Strand KM, Solberg P, Tappert C, Araya E, Bærheim G, Lyslo I, Tollaksen K, Bjørge L, Austgulen R.

BMC Pregnancy Childbirth. 2015 Dec 1;15:319. doi: 10.1186/s12884-015-0754-2.

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