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Results: 1 to 20 of 77


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 Apr 29. doi: 10.1002/ajmg.a.37129. [Epub ahead of print]


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 Apr 22. pii: S0002-9394(15)00229-9. doi: 10.1016/j.ajo.2015.04.026. [Epub ahead of print]


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.


The feasibility of genetic dissection of endophenotypes.

Wilhelmsen KC.

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


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.


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.


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.


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.


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.


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.


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.


Genome-wide scan for copy number variation association with age at onset of Alzheimer's disease.

Szigeti K, Lal D, Li Y, Doody RS, Wilhelmsen K, Yan L, Liu S, Ma C; Texas Alzheimer Research and Care Consortium.

J Alzheimers Dis. 2013;33(2):517-23. doi: 10.3233/JAD-2012-121285.


Serum granulocyte colony-stimulating factor and Alzheimer's disease.

Barber RC, Edwards MI, Xiao G, Huebinger RM, Diaz-Arrastia R, Wilhelmsen KC, Hall JR, O'Bryant SE.

Dement Geriatr Cogn Dis Extra. 2012 Jan;2(1):353-60. Epub 2012 Aug 29.


An informatics approach to analyzing the incidentalome.

Berg JS, Adams M, Nassar N, Bizon C, Lee K, Schmitt CP, Wilhelmsen KC, Evans JP.

Genet Med. 2013 Jan;15(1):36-44. doi: 10.1038/gim.2012.112. Epub 2012 Sep 20.


ReQON: a Bioconductor package for recalibrating quality scores from next-generation sequencing data.

Cabanski CR, Cavin K, Bizon C, Wilkerson MD, Parker JS, Wilhelmsen KC, Perou CM, Marron JS, Hayes DN.

BMC Bioinformatics. 2012 Sep 4;13:221.


Genome-wide linkage scan of antisocial behavior, depression, and impulsive substance use in the UCSF family alcoholism study.

Gizer IR, Ehlers CL, Vieten C, Feiler HS, Gilder DA, Wilhelmsen KC.

Psychiatr Genet. 2012 Oct;22(5):235-44. doi: 10.1097/YPG.0b013e328353fb77.


Significance of genomic rearrangements in epilepsy.

Wilhelmsen KC.

Arch Neurol. 2012 Mar;69(3):305-7. doi: 10.1001/archneurol.2011.3256. No abstract available.


Localized hippocampus measures are associated with Alzheimer pathology and cognition independent of total hippocampal volume.

Carmichael O, Xie J, Fletcher E, Singh B, DeCarli C; Alzheimer's Disease Neuroimaging Initiative.

Neurobiol Aging. 2012 Jun;33(6):1124.e31-41. doi: 10.1016/j.neurobiolaging.2011.08.016. Epub 2011 Dec 14.


A blood-based screening tool for Alzheimer's disease that spans serum and plasma: findings from TARC and ADNI.

O'Bryant SE, Xiao G, Barber R, Huebinger R, Wilhelmsen K, Edwards M, Graff-Radford N, Doody R, Diaz-Arrastia R; Texas Alzheimer's Research & Care Consortium; Alzheimer's Disease Neuroimaging Initiative.

PLoS One. 2011;6(12):e28092. doi: 10.1371/journal.pone.0028092. Epub 2011 Dec 7.


Detecting global and local hippocampal shape changes in Alzheimer's disease using statistical shape models.

Shen KK, Fripp J, Mériaudeau F, Chételat G, Salvado O, Bourgeat P; Alzheimer's Disease Neuroimaging Initiative.

Neuroimage. 2012 Feb 1;59(3):2155-66. doi: 10.1016/j.neuroimage.2011.10.014. Epub 2011 Oct 14.

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