APOE is not associated with Alzheimer Disease: a cautionary tale of genotype imputation

di Beecham, Gary W., Martin, Eden R., Gilbert, John R., Haines, Jonathan L., Pericak-Vance, Margaret A.
Pubblicazione 2010

Resolving the Relationship between Apolipoprotein E and Depression

di Slifer, Michael A., Martin, Eden R., Gilbert, John R., Haines, Jonathan L., Pericak-Vance, Margaret A.
Pubblicazione 2009

Human Neural Tube Defects: Developmental Biology, Epidemiology, and Genetics

di Detrait, Eric.R., George, Timothy. M., Etchevers, Heather.C., Gilbert, John.R., Vekemans, Michel., Speer, Marcy. C.
Pubblicazione 2005

PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility

di Beecham, Gary W, Naj, Adam, Gilbert, John R, Haines, Jonathan L, Buxbaum, Joseph D, Pericak-Vance, Margaret A
Pubblicazione 2010

Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorder

di Griswold, Anthony J., Van Booven, Derek, Cuccaro, Michael, Haines, Jonathan L., Gilbert, John R., Pericak-Vance, Margaret A.
Pubblicato in Neurogenetics (2017)

Specific Regional Transcription of Apolipoprotein E in Human Brain Neurons

di Xu, Pu-Ting, Gilbert, John R., Qiu, Hui-Ling, Ervin, John, Rothrock-Christian, Tracie R., Hulette, Christine, Schmechel, Donald E.
Pubblicazione 1999

A Role for apoE in Regulating the Levels of α-1-Antichymotrypsin in the Aging Mouse Brain and in Alzheimer’s Disease

di Licastro, Federico, Campbell, Iain L., Kincaid, Carrie, Veinbergs, Isaac, Van Uden, Emily, Rockenstein, Edward, Mallory, Margaret, Gilbert, John R., Masliah, Eliezer
Pubblicazione 1999

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation

di Carney, Regina M., Kohli, Martin A., Kunkle, Brian W., Naj, Adam C., Gilbert, John R., Züchner, Stephan, Pericak-Vance, Margaret A.
Pubblicazione 2013

Novel approach for independent control of brain hypothermia and systemic normothermia: cerebral selective deep hypothermia for refractory cardiac arrest

di Wang, Chih-Hsien, Lin, Yu-Ting, Chou, Heng-Wen, Wang, Yi-Chih, Hwang, Joey-Jen, Gilbert, John R, Chen, Yih-Sharng
Pubblicato in BMJ Case Rep (2017)

Novel approach for independent control of brain hypothermia and systemic normothermia: cerebral selective deep hypothermia for refractory cardiac arrest

di Wang, Chih-Hsien, Lin, Yu-Ting, Chou, Heng-Wen, Wang, Yi-Chih, Hwang, Joey-Jen, Gilbert, John R, Chen, Yih-Sharng
Pubblicato in J Neurointerv Surg (2017)

Genome-wide Association Study Implicates a Chromosome 12 Risk Locus for Late-Onset Alzheimer Disease

di Beecham, Gary W., Martin, Eden R., Li, Yi-Ju, Slifer, Michael A., Gilbert, John R., Haines, Jonathan L., Pericak-Vance, Margaret A.
Pubblicazione 2009

A comparative analysis of the information content in long and short SAGE libraries

di Li, Yi-Ju, Xu, Puting, Qin, Xuejun, Schmechel, Donald E, Hulette, Christine M, Haines, Jonathan L, Pericak-Vance, Margaret A, Gilbert, John R
Pubblicazione 2006

Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10

di Liang, Xueying, Slifer, Michael, Martin, Eden R., Schnetz-Boutaud, Nathalie, Bartlett, Jackie, Anderson, Brent, Züchner, Stephan, Gwirtsman, Harry, Gilbert, John R., Pericak-Vance, Margaret A., Haines, Jonathan L.
Pubblicazione 2009

Identification of Chromosome 7 Inversion Breakpoints in an Autistic Family Narrows Candidate Region for Autism Susceptibility

di Cukier, Holly N., Skaar, David A., Rayner-Evans, Melissa Y., Konidari, Ioanna, Whitehead, Patrice L., Jaworski, James M., Cuccaro, Michael L., Pericak-Vance, Margaret A., Gilbert, John R.
Pubblicato in Autism Res (2009)

High Density SNP Screen in A Large Multiplex Neural Tube Defect Family Refines Linkage to Loci at 7p21-Pter And 2q33.1-35

di Stamm, Demetra S., Rampersaud, Evadnie, Slifer, Susan H., Mehltretter, Lorraine, Siegel, Deborah G., Xie, Jianzhen, Hu-Lince, Diane, Craig, David W., Stephan, Dietrich A., George, Timothy M., Gilbert, John R., Speer, Marcy C.
Pubblicazione 2006

Investigation of autism and GABA receptor subunit genes in multiple ethnic groups

di Collins, Ann L., Ma, Deqiong, Whitehead, Patrice L., Martin, Eden R., Wright, Harry H., Abramson, Ruth K., Hussman, John P., Haines, Jonathan L., Cuccaro, Michael L., Gilbert, John R., Pericak-Vance, Margaret A.
Pubblicazione 2006

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals

di Cukier, Holly N., Rabionet, Raquel, Konidari, Ioanna, Rayner-Evans, Melissa Y., Baltos, Mary L., Wright, Harry H., Abramson, Ruth K., Martin, Eden R., Cuccaro, Michael L., Pericak-Vance, Margaret A., Gilbert, John R.
Pubblicazione 2009

Successful aging shows linkage to chromosomes 6, 7, and 14 in the Amish

di EDWARDS, DIGNA R. VELEZ, GILBERT, JOHN R., JIANG, LAN, GALLINS, PAUL J., CAYWOOD, LAURA, CREASON, MARILYN, FUZZELL, DENISE, KNEBUSCH, CLARE, JACKSON, CHARLES E., PERICAK-VANCE, MARGARET A., HAINES, JONATHAN L., SCOTT, WILLIAM K.
Pubblicazione 2011

Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12

di Weeks Daniel E, Gilbert John R, De La Paz Monica A, Hauser Elizabeth R, Agarwal Anita, Postel Eric A, Scott William K, Schmidt Silke, Gorin Michael B, Haines Jonathan L, Pericak-Vance Margaret A
Pubblicazione 2004-07-01

Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12

di Schmidt, Silke, Scott, William K, Postel, Eric A, Agarwal, Anita, Hauser, Elizabeth R, De La Paz, Monica A, Gilbert, John R, Weeks, Daniel E, Gorin, Michael B, Haines, Jonathan L, Pericak-Vance, Margaret A
Pubblicazione 2004