(U01GM62378 OR UO1GM62378 OR GM62378 OR U01HL69757 OR UO1HL69757 OR HL69757 OR (GM61390 OR "GM 61390") OR ("U01 HL69758" OR HL69758 NOT 12523655[UID]) OR "U01 HL65962" OR HL65962 OR "U01 GM61373" OR GM61373 OR 12893988[UID] OR 12798184[UID] OR 12676886[UID] OR 12668916[UID] OR 12629575[UID] OR 12544507[UID] OR "U01 ES10867" OR 12223053[UID] OR "U01 HL65899" OR "UO1 HL65899" OR HL65899 OR 11306963[UID] OR 11371409[UID] OR 12958057[UID] OR 12890927[UID] OR 9988463[UID] OR 9641598[UID] OR 12582322[UID] OR 11934710[UID] OR 11913724[UID] OR 11804270[UID] OR 10971202[UID] OR 10669529[UID] OR ("U01 GM63340" OR "UO1 GM63340" OR UO1GM63340 OR GM63340 OR GM63340-01 OR "1U01 GM63340") OR 12112247[UID] OR 12203989[UID] OR 12559764[UID] OR 12480661[UID] OR 14500593[UID] OR 12517285[UID] OR (U01GM61394 NOT 11875363[UID] NOT 12571262[UID]) OR 12476326[UID] OR 12476313[UID] OR 12457157[UID] OR 12439730[UID] OR 12196906[UID] OR 12140770[UID] OR 12082580[UID] OR 12049176[UID] OR 11911443[UID] OR 11908753[UID] OR 11443202[UID] OR 11331918[UID] OR 11274427[UID] OR 10890909[UID] OR "U01 GM61388" OR "UO1 GM61388" OR 11549275[UID] OR 12517278[UID] OR 11990382[UID] OR 12223053[UID] OR "U01 GM61393" OR U01GM61393 OR GM61393 OR 12202670[UID] OR 12406645[UID] OR 12499391[UID] OR 12065767[UID] OR 12544509[UID] OR 12704389[UID] OR 12893990[UID] OR 12665971[UID] OR 12631599[UID] OR 12196214[UID] OR 11905809[UID] OR 12835618[UID] OR 14528287[UID] OR 12969965[UID] OR 14578886[UID] OR ("U01 GM61374" OR U01GM61374 OR GM61374 AND Stanford) OR 12546913[UID] OR 12544507[UID] OR 12463865[UID] OR 12386112[UID] OR 12368251[UID] OR 12169549[UID])

1.

A case of premature thelarche with no central cause or genetic variants within the estrogen receptor signaling pathway.

Hartmaier RJ, Walenkamp MJ, Richter AS, Wang J, Katzenellenbogen BS, Oesterreich S, Wit JM.

J Pediatr Endocrinol Metab. 2009 Aug;22(8):751-8.PMID: 19845126 [PubMed - indexed for MEDLINE]Related articles

2.

GRK5 Gln41Leu polymorphism is not associated with sensitivity to beta(1)-adrenergic blockade in humans.

Kurnik D, Cunningham AJ, Sofowora GG, Kohli U, Li C, Friedman EA, Muszkat M, Menon UB, Wood AJ, Stein CM.

Pharmacogenomics. 2009 Oct;10(10):1581-7.PMID: 19842931 [PubMed - in process]Related articles

3.

Institutional Profile: The University of California Pharmacogenomics Center: at the interface of genomics, biological mechanisms and drug therapy.

Kroetz DL, Ahituv N, Burchard EG, Guo S, Sali A, Giacomini KM.

Pharmacogenomics. 2009 Oct;10(10):1569-76.PMID: 19842929 [PubMed - in process]Related articles

4.

Mutations in sodium channel beta1- and beta2-subunits associated with atrial fibrillation.

Watanabe H, Darbar D, Kaiser DW, Jiramongkolchai K, Chopra S, Donahue BS, Kannankeril PJ, Roden DM.

Circ Arrhythm Electrophysiol. 2009 Jun;2(3):268-75. Epub 2009 Mar 6.PMID: 19808477 [PubMed - indexed for MEDLINE]Related articles

5.

Gene set enrichment analyses revealed differences in gene expression patterns between males and females.

Zhang W, Huang RS, Duan S, Dolan ME.

In Silico Biol. 2009;9(3):55-63.PMID: 19795565 [PubMed - indexed for MEDLINE]Related articles Free article

6.

Patterns of pharmacogenetic diversity in African populations: role of ancient and recent history.

Oliveira E, Pereira R, Amorim A, McLeod H, Prata MJ.

Pharmacogenomics. 2009 Sep;10(9):1413-22.PMID: 19761365 [PubMed - in process]Related articles

7.

Predicting response to short-acting bronchodilator medication using Bayesian networks.

Himes BE, Wu AC, Duan QL, Klanderman B, Litonjua AA, Tantisira K, Ramoni MF, Weiss ST.

Pharmacogenomics. 2009 Sep;10(9):1393-412.PMID: 19761364 [PubMed - in process]Related articles

8.

Identification and characterization of novel polymorphisms in the basal promoter of the human transporter, MATE1.

Ha Choi J, Wah Yee S, Kim MJ, Nguyen L, Ho Lee J, Kang JO, Hesselson S, Castro RA, Stryke D, Johns SJ, Kwok PY, Ferrin TE, Goo Lee M, Black BL, Ahituv N, Giacomini KM.

Pharmacogenet Genomics. 2009 Oct;19(10):770-80.PMID: 19745787 [PubMed - in process]Related articles

9.

A pharmacogene database enhanced by the 1000 Genomes Project.

Gamazon ER, Zhang W, Huang RS, Dolan ME, Cox NJ.

Pharmacogenet Genomics. 2009 Oct;19(10):829-32.PMID: 19745786 [PubMed - in process]Related articles

10.

Genetic variation in the proximal promoter of ABC and SLC superfamilies: liver and kidney specific expression and promoter activity predict variation.

Hesselson SE, Matsson P, Shima JE, Fukushima H, Yee SW, Kobayashi Y, Gow JM, Ha C, Ma B, Poon A, Johns SJ, Stryke D, Castro RA, Tahara H, Choi JH, Chen L, Picard N, Sjödin E, Roelofs MJ, Ferrin TE, Myers R, Kroetz DL, Kwok PY, Giacomini KM.

PLoS One. 2009 Sep 9;4(9):e6942.PMID: 19742321 [PubMed - in process]Related articles Free article

11.

Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.

Verlaan DJ, Berlivet S, Hunninghake GM, Madore AM, Larivière M, Moussette S, Grundberg E, Kwan T, Ouimet M, Ge B, Hoberman R, Swiatek M, Dias J, Lam KC, Koka V, Harmsen E, Soto-Quiros M, Avila L, Celedón JC, Weiss ST, Dewar K, Sinnett D, Laprise C, Raby BA, Pastinen T, Naumova AK.

Am J Hum Genet. 2009 Sep;85(3):377-93.PMID: 19732864 [PubMed - indexed for MEDLINE]Related articles

12.

Predicting drug side-effects by chemical systems biology.

Tatonetti NP, Liu T, Altman RB.

Genome Biol. 2009;10(9):238. Epub 2009 Sep 2.PMID: 19723347 [PubMed - in process]Related articles

13.

Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org).

Postema PG, Wolpert C, Amin AS, Probst V, Borggrefe M, Roden DM, Priori SG, Tan HL, Hiraoka M, Brugada J, Wilde AA.

Heart Rhythm. 2009 Sep;6(9):1335-41. Epub 2009 Jul 8.PMID: 19716089 [PubMed - in process]Related articles

14.

Cardiovascular pharmacogenomics and individualized drug therapy.

Pereira NL, Weinshilboum RM.

Nat Rev Cardiol. 2009 Oct;6(10):632-8. Epub 2009 Aug 25.PMID: 19707183 [PubMed - in process]Related articles

15.

A novel pathway of insulin sensitivity in chromogranin a null mice: a crucial role for pancreastatin in glucose homeostasis.

Gayen JR, Saberi M, Schenk S, Biswas N, Vaingankar SM, Cheung WW, Najjar SM, O'Connor DT, Bandyopadhyay G, Mahata SK.

J Biol Chem. 2009 Oct 16;284(42):28498-509. Epub 2009 Aug 25.PMID: 19706599 [PubMed - in process]Related articles

16.

Recommendations for using standardised phenotypes in genetic association studies.

Naylor MG, Weiss ST, Lange C.

Hum Genomics. 2009 Jul;3(4):308-19.PMID: 19706362 [PubMed - indexed for MEDLINE]Related articles

17.

Germline genomic variants associated with childhood acute lymphoblastic leukemia.

Treviño LR, Yang W, French D, Hunger SP, Carroll WL, Devidas M, Willman C, Neale G, Downing J, Raimondi SC, Pui CH, Evans WE, Relling MV.

Nat Genet. 2009 Sep;41(9):1001-5. Epub 2009 Aug 16.PMID: 19684603 [PubMed - indexed for MEDLINE]Related articles

18.

Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs.

Rana BK, Wessel J, Mahboubi V, Rao F, Haeller J, Gayen JR, Eskin E, Valle AM, Das M, Mahata SK, Taupenot L, Stridsberg M, Talley TT, Ziegler MG, Smith DW, Schork NJ, O'Connor DT, Taylor P.

J Pharmacol Exp Ther. 2009 Nov;331(2):419-28. Epub 2009 Aug 11.PMID: 19671882 [PubMed - in process]Related articles

19.

Genetics and pharmacogenetics of the leukotriene pathway.

Tantisira KG, Drazen JM.

J Allergy Clin Immunol. 2009 Sep;124(3):422-7. Epub 2009 Aug 8. Review.PMID: 19665766 [PubMed - indexed for MEDLINE]Related articles

20.

Predictors of poor response during asthma therapy differ with definition of outcome.

Rogers AJ, Tantisira KG, Fuhlbrigge AL, Litonjua AA, Lasky-Su JA, Szefler SJ, Strunk RC, Zeiger RS, Weiss ST.

Pharmacogenomics. 2009 Aug;10(8):1231-42.PMID: 19663668 [PubMed - in process]Related articles

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