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Items: 1 to 20 of 78

1.

Genetic variation in FAAH is associated with cannabis use disorders in a young adult sample of Mexican Americans.

Melroy-Greif WE, Wilhelmsen KC, Ehlers CL.

Drug Alcohol Depend. 2016 Jun 25. pii: S0376-8716(16)30168-5. doi: 10.1016/j.drugalcdep.2016.06.021. [Epub ahead of print]

PMID:
27394933
2.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Green RC, Goddard KA, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W, Caga-Anan CF, Chinnaiyan AM, Chung WK, Clayton EW, Cooper GM, East K, Evans JP, Fullerton SM, Garraway LA, Garrett JR, Gray SW, Henderson GE, Hindorff LA, Holm IA, Lewis MH, Hutter CM, Janne PA, Joffe S, Kaufman D, Knoppers BM, Koenig BA, Krantz ID, Manolio TA, McCullough L, McEwen J, McGuire A, Muzny D, Myers RM, Nickerson DA, Ou J, Parsons DW, Petersen GM, Plon SE, Rehm HL, Roberts JS, Robinson D, Salama JS, Scollon S, Sharp RR, Shirts B, Spinner NB, Tabor HK, Tarczy-Hornoch P, Veenstra DL, Wagle N, Weck K, Wilfond BS, Wilhelmsen K, Wolf SM, Wynn J, Yu JH; CSER Consortium.

Am J Hum Genet. 2016 Jul 7;99(1):246. doi: 10.1016/j.ajhg.2016.06.002. No abstract available.

PMID:
27392080
3.

A New Framework and Prototype Solution for Clinical Decision Support and Research in Genomics and Other Data-intensive Fields of Medicine.

Evans JP, Wilhelmsen KC, Berg J, Schmitt CP, Krishnamurthy A, Fecho K, Ahalt SC.

EGEMS (Wash DC). 2016 Apr 19;4(1):1198. doi: 10.13063/2327-9214.1198. eCollection 2016.

4.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Green RC, Goddard KA, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W, Caga-Anan CF, Chinnaiyan AM, Chung WK, Clayton EW, Cooper GM, East K, Evans JP, Fullerton SM, Garraway LA, Garrett JR, Gray SW, Henderson GE, Hindorff LA, Holm IA, Lewis MH, Hutter CM, Janne PA, Joffe S, Kaufman D, Knoppers BM, Koenig BA, Krantz ID, Manolio TA, McCullough L, McEwen J, McGuire A, Muzny D, Myers RM, Nickerson DA, Ou J, Parsons DW, Petersen GM, Plon SE, Rehm HL, Roberts JS, Robinson D, Salama JS, Scollon S, Sharp RR, Shirts B, Spinner NB, Tabor HK, Tarczy-Hornoch P, Veenstra DL, Wagle N, Weck K, Wilfond BS, Wilhelmsen K, Wolf SM, Wynn J, Yu JH; CSER Consortium.

Am J Hum Genet. 2016 Jun 2;98(6):1051-66. doi: 10.1016/j.ajhg.2016.04.011. Epub 2016 May 12.

PMID:
27181682
5.

Common susceptibility variants are shared between schizophrenia and psoriasis in the Han Chinese population.

Yin X, Wineinger NE, Wang K, Yue W, Norgren N, Wang L, Yao W, Jiang X, Wu B, Cui Y, Shen C, Cheng H, Zhou F, Chen G, Zuo X, Zheng X, Fan X, Wang H, Wang L, Lee J, Lam M, Tai ES, Zhang Z, Huang Q, Sun L, Xu J, Yang S, Wilhelmsen KC, Liu J, Schork NJ, Zhang X.

J Psychiatry Neurosci. 2016 Apr 18;41(4):150210. doi: 10.1503/jpn.150210. [Epub ahead of print]

6.

Germline Analysis from Tumor-Germline Sequencing Dyads to identify clinically actionable secondary findings.

Seifert BA, O'Daniel JM, Amin K, Marchuk DS, Patel NM, Parker JS, Hoyle AP, Mose LE, Marron A, Hayward MC, Bizon C, Wilhelmsen KC, Evans JP, Earp HS, Sharpless N, Hayes DN, Berg JS.

Clin Cancer Res. 2016 Apr 15. pii: clincanres.0015.2016. [Epub ahead of print]

PMID:
27083775
7.

Can Genetic Analysis of Putative Blood Alzheimer's Disease Biomarkers Lead to Identification of Susceptibility Loci?

Barber RC, Phillips NR, Tilson JL, Huebinger RM, Shewale SJ, Koenig JL, Mitchel JS, O'Bryant SE, Waring SC, Diaz-Arrastia R, Chasse S, Wilhelmsen KC; Alzheimer’s Disease Neuroimaging Initiative; Texas Alzheimer’s Research and Care Consortium.

PLoS One. 2015 Dec 1;10(12):e0142360. doi: 10.1371/journal.pone.0142360. eCollection 2015.

8.

Variants Near CCK Receptors are Associated With Electrophysiological Responses to Pre-pulse Startle Stimuli in a Mexican American Cohort.

Norden-Krichmar TM, Gizer IR, Phillips E, Wilhelmsen KC, Schork NJ, Ehlers CL.

Twin Res Hum Genet. 2015 Dec;18(6):727-37. doi: 10.1017/thg.2015.77. Epub 2015 Nov 26.

PMID:
26608796
9.

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing.

Berg JS, Foreman AK, O'Daniel JM, Booker JK, Boshe L, Carey T, Crooks KR, Jensen BC, Juengst ET, Lee K, Nelson DK, Powell BC, Powell CM, Roche MI, Skrzynia C, Strande NT, Weck KE, Wilhelmsen KC, Evans JP.

Genet Med. 2016 May;18(5):467-75. doi: 10.1038/gim.2015.104. Epub 2015 Aug 13.

10.

The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: report and review.

Couser NL, Masood MM, Strande NT, Foreman AK, Crooks K, Weck KE, Lu M, Wilhelmsen KC, Roche M, Evans JP, Berg JS, Powell CM.

Am J Med Genet A. 2015 Sep;167A(9):2176-81. doi: 10.1002/ajmg.a.37129. Epub 2015 Apr 29.

PMID:
25920937
11.

High Diagnostic Yield of Whole Exome Sequencing in Participants With Retinal Dystrophies in a Clinical Ophthalmology Setting.

Lee K, Berg JS, Milko L, Crooks K, Lu M, Bizon C, Owen P, Wilhelmsen KC, Weck KE, Evans JP, Garg S.

Am J Ophthalmol. 2015 Aug;160(2):354-363.e9. doi: 10.1016/j.ajo.2015.04.026. Epub 2015 Apr 22.

PMID:
25910913
12.

Protective variant associated with alcohol dependence in a Mexican American cohort.

Norden-Krichmar TM, Gizer IR, Wilhelmsen KC, Schork NJ, Ehlers CL.

BMC Med Genet. 2014 Dec 21;15:136. doi: 10.1186/s12881-014-0136-z.

13.

The feasibility of genetic dissection of endophenotypes.

Wilhelmsen KC.

Psychophysiology. 2014 Dec;51(12):1337-8. doi: 10.1111/psyp.12366.

PMID:
25387719
14.

Association and ancestry analysis of sequence variants in ADH and ALDH using alcohol-related phenotypes in a Native American community sample.

Peng Q, Gizer IR, Libiger O, Bizon C, Wilhelmsen KC, Schork NJ, Ehlers CL.

Am J Med Genet B Neuropsychiatr Genet. 2014 Dec;165B(8):673-83. doi: 10.1002/ajmg.b.32272. Epub 2014 Sep 30.

15.

Correlation analysis of genetic admixture and social identification with body mass index in a Native American community.

Norden-Krichmar TM, Gizer IR, Libiger O, Wilhelmsen KC, Ehlers CL, Schork NJ.

Am J Hum Biol. 2014 May-Jun;26(3):347-60. doi: 10.1002/ajhb.22521. Epub 2014 Feb 17.

16.

GCH1 heterozygous mutation identified by whole-exome sequencing as a treatable condition in a patient presenting with progressive spastic paraplegia.

Fan Z, Greenwood R, Felix AC, Shiloh-Malawsky Y, Tennison M, Roche M, Crooks K, Weck K, Wilhelmsen K, Berg J, Evans J.

J Neurol. 2014 Mar;261(3):622-4. doi: 10.1007/s00415-014-7265-3. Epub 2014 Feb 8. No abstract available.

17.

Variant calling in low-coverage whole genome sequencing of a Native American population sample.

Bizon C, Spiegel M, Chasse SA, Gizer IR, Li Y, Malc EP, Mieczkowski PA, Sailsbery JK, Wang X, Ehlers CL, Wilhelmsen KC.

BMC Genomics. 2014 Jan 30;15:85. doi: 10.1186/1471-2164-15-85.

18.

Molecular neuropsychology: creation of test-specific blood biomarker algorithms.

O'Bryant SE, Xiao G, Barber R, Cullum CM, Weiner M, Hall J, Edwards M, Grammas P, Wilhelmsen K, Doody R, Diaz-Arrastia R; Texas Alzheimer’s Research and Care Consortium.

Dement Geriatr Cogn Disord. 2014;37(1-2):45-57. doi: 10.1159/000345605. Epub 2013 Jan 3.

19.

Visual aids to medical data and computational diagnostics: new frontiers in pediatric neurology.

Mane KK, Loddenkemper T, Fernández IS, Mikati MA, Tennison M, Schmitt C, Wilhelmsen K, Leviton A.

Epilepsy Behav. 2013 Aug;28(2):258-60. doi: 10.1016/j.yebeh.2013.04.014. Epub 2013 Jun 4. No abstract available.

PMID:
23756296
20.

Contributions of ethnicity to differential item functioning of cannabis abuse and dependence symptoms.

Gizer IR, Gilder DA, Lau P, Wang T, Wilhelmsen KC, Ehlers CL.

J Stud Alcohol Drugs. 2013 Mar;74(2):320-8.

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