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John R. Gilbert, PhD - Publications

Affiliations: 
Human Genetics University of Miami, Coral Gables, FL 
Area:
http://www.researchprofiles.collexis.com/jad/expert.asp?u_id=146
Website:
http://www.mihg.org/weblog/people/2008/03/john-r-gilbert.html

236 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Cukier HN, Griswold AJ, Hofmann NK, Gomez L, Whitehead PL, Abramson RK, Gilbert JR, Cuccaro ML, Dykxhoorn DM, Pericak-Vance MA. Three Brothers With Autism Carry a Stop-Gain Mutation in the HPA-Axis Gene NR3C2. Autism Research : Official Journal of the International Society For Autism Research. PMID 32064789 DOI: 10.1002/Aur.2269  0
2019 Goldschmidt-Clermont PJ, Volinsky FG, LaRosa SP, Gilbert JR, Periçak-Vance MA. Time for Well-Powered Controlled Prospective Studies to test a Causal Role for Herpes Viruses in Alzheimer Using Anti-Herpes Drugs. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 31175818 DOI: 10.1093/Gerona/Glz150  0
2017 Griswold AJ, Van Booven D, Cuccaro ML, Haines JL, Gilbert JR, Pericak-Vance MA. Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorder. Neurogenetics. PMID 29151244 DOI: 10.1007/S10048-017-0529-1  0
2017 Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... Gilbert JR, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916  0
2017 . Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Molecular Autism. 8: 21. PMID 28540026 DOI: 10.1186/S13229-017-0137-9  0
2017 Wang CH, Lin YT, Chou HW, Wang YC, Hwang JJ, Gilbert JR, Chen YS. Novel approach for independent control of brain hypothermia and systemic normothermia: cerebral selective deep hypothermia for refractory cardiac arrest. Journal of Neurointerventional Surgery. PMID 28122916 DOI: 10.1136/neurintsurg-2016-012806.rep  0.36
2017 Wang CH, Lin YT, Chou HW, Wang YC, Hwang JJ, Gilbert JR, Chen YS. Novel approach for independent control of brain hypothermia and systemic normothermia: cerebral selective deep hypothermia for refractory cardiac arrest. Bmj Case Reports. 2017. PMID 28108436 DOI: 10.1136/bcr-2016-012806  0.36
2016 Cukier HN, Kunkle BW, Vardarajan BN, Rolati S, Hamilton-Nelson KL, Kohli MA, Whitehead PL, Dombroski BA, Van Booven D, Lang R, Dykxhoorn DM, Farrer LA, Cuccaro ML, Vance JM, Gilbert JR, et al. ABCA7 frameshift deletion associated with Alzheimer disease in African Americans. Neurology. Genetics. 2: e79. PMID 27231719 DOI: 10.1016/J.Jalz.2016.06.305  0.01
2016 Kohli MA, Cukier HN, Hamilton-Nelson KL, Rolati S, Kunkle BW, Whitehead PL, Züchner SL, Farrer LA, Martin ER, Beecham GW, Haines JL, Vance JM, Cuccaro ML, Gilbert JR, Schellenberg GD, et al. Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease. Neurology. Genetics. 2: e41. PMID 27066578 DOI: 10.1212/Nxg.0000000000000041  0.01
2016 Ridge PG, Hoyt KB, Boehme K, Mukherjee S, Crane PK, Haines JL, Mayeux R, Farrer LA, Pericak-Vance MA, Schellenberg GD, Kauwe JS. Assessment of the genetic variance of late-onset Alzheimer's disease. Neurobiology of Aging. PMID 27036079 DOI: 10.1016/J.Neurobiolaging.2016.02.024  0
2016 Hicks JE, Konidari I, Scott BL, Stajich JM, Ashley-Koch AE, Gilbert JR, Scott WK. Linkage of familial essential tremor to chromosome 5q35. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 26918299 DOI: 10.1002/Mds.26582  0.01
2016 Traylor M, Adib-Samii P, Harold D, Dichgans M, Williams J, Lewis CM, Markus HS. Shared genetic contribution to Ischaemic Stroke and Alzheimer's Disease. Annals of Neurology. PMID 26913989 DOI: 10.1002/Ana.24621  0
2016 Xu P, Thomas S, Dellinger A, Etchevers H, Vekemans M, Gilbert JR, Speer MC. Transcriptome analysis of genes involved in neural tube closure during human embryonic development using Long-SAGE F1000research. 5. DOI: 10.7490/F1000Research.1111340.1  0
2016 Cukier HN, Kunkle BW, Rolati S, Whitehead PL, Vance JM, Cuccaro ML, Carney RM, Gilbert JR, Martin ER, Beecham GW, Haines JL, Pericak-Vance MA, Hamilton-Nelson KL. O1-09-02: Whole Exome Sequencing of Late Onset Multiplex Families Identifies Rare Coding Variants in Known and Novel Alzheimer’s Disease Genes Alzheimer's & Dementia. 12: P196-P197. DOI: 10.1016/J.Jalz.2016.06.342  0
2016 Sayers RL, Gethings L, Wallace A, Semic-Jusufgic A, Simpson A, Barran P, Gilbert J, Senyuva H, Rodgers A, Bromley M, Walker M, Brown H, Mills ENC. How Much of a Problem Is Peanut in Ground Cumin for Individuals with Peanut Allergy The Journal of Allergy and Clinical Immunology. 137. DOI: 10.1016/J.Jaci.2015.12.597  0
2015 Lowe MR, Arigo D, Butryn ML, Gilbert JR, Sarwer D, Stice E. Hedonic Hunger Prospectively Predicts Onset and Maintenance of Loss of Control Eating Among College Women. Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association. PMID 26690638 DOI: 10.1037/Hea0000291  0.01
2015 Gilbert JR, Symmonds M, Hanna MG, Dolan RJ, Friston KJ, Moran RJ. Profiling neuronal ion channelopathies with non-invasive brain imaging and dynamic causal models: Case studies of single gene mutations. Neuroimage. 124: 43-53. PMID 26342528 DOI: 10.1016/J.Neuroimage.2015.08.057  0.01
2015 Annangudi SP, Myung K, Avila Adame C, Bowling AJ, Dasari M, Gilbert JR. Response to Comment on "MALDI-MS Imaging Analysis of Fungicide Residue Distributions on Wheat Leaf Surfaces". Environmental Science & Technology. 49: 10747-9. PMID 26266690 DOI: 10.1021/acs.est.5b03670  0.2
2015 Griswold AJ, Dueker ND, Van Booven D, Rantus JA, Jaworski JM, Slifer SH, Schmidt MA, Hulme W, Konidari I, Whitehead PL, Cuccaro ML, Martin ER, Haines JL, Gilbert JR, Hussman JP, et al. Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants. Molecular Autism. 6: 43. PMID 26185613 DOI: 10.1186/S13229-015-0034-Z  0.04
2015 Mukherjee S, Walter S, Kauwe JS, Saykin AJ, Bennett DA, Larson EB, Crane PK, Glymour MM. Genetically predicted body mass index and Alzheimer's disease-related phenotypes in three large samples: Mendelian randomization analyses. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 26079416 DOI: 10.1016/j.jalz.2015.05.015  0.16
2015 Humphries C, Kohli MA, Whitehead P, Mash DC, Pericak-Vance MA, Gilbert J. Alzheimer disease (AD) specific transcription, DNA methylation and splicing in twenty AD associated loci. Molecular and Cellular Neurosciences. 67: 37-45. PMID 26004081 DOI: 10.1016/J.Mcn.2015.05.003  0
2015 Kozol RA, Cukier HN, Zou B, Mayo V, De Rubeis S, Cai G, Griswold AJ, Whitehead PL, Haines JL, Gilbert JR, Cuccaro ML, Martin ER, Baker JD, Buxbaum JD, Pericak-Vance MA, et al. Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis. Human Molecular Genetics. 24: 4006-23. PMID 25882707 DOI: 10.1093/Hmg/Ddv138  0.16
2015 Annangudi SP, Myung K, Avila Adame C, Gilbert JR. MALDI-MS Imaging Analysis of Fungicide Residue Distributions on Wheat Leaf Surfaces. Environmental Science & Technology. 49: 5579-83. PMID 25830667 DOI: 10.1021/es506334y  0.2
2015 Wang D, Gilbert JR, Shaw MA, Shakir S, Losee JE, Billiar TR, Cooper GM. Toll-like receptor 4 mediates the regenerative effects of bone grafts for calvarial bone repair. Tissue Engineering. Part A. 21: 1299-308. PMID 25603990 DOI: 10.1089/ten.TEA.2014.0215  0.04
2015 . Convergent genetic and expression data implicate immunity in Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 11: 658-71. PMID 25533204 DOI: 10.1016/J.Jalz.2014.05.1757  0
2015 Wang LS, Naj AC, Graham RR, Crane PK, Kunkle BW, Cruchaga C, Murcia JD, Cannon-Albright L, Baldwin CT, Zetterberg H, Blennow K, Kukull WA, Faber KM, Schupf N, Norton MC, ... Gilbert JR, et al. Rarity of the Alzheimer disease-protective APP A673T variant in the United States. Jama Neurology. 72: 209-16. PMID 25531812 DOI: 10.1001/Jamaneurol.2014.2157  0.16
2015 Humphries CE, Kohli MA, Nathanson L, Whitehead P, Beecham G, Martin E, Mash DC, Pericak-Vance MA, Gilbert J. Integrated whole transcriptome and DNA methylation analysis identifies gene networks specific to late-onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 44: 977-87. PMID 25380588 DOI: 10.3233/Jad-141989  0
2015 Griswold AJ, Dueker ND, Booven D, Rantus JA, Jaworski JM, Slifer SH, Schmidt MA, Hulme W, Konidari I, Whitehead PL, Cuccaro ML, Martin ER, Haines JL, Gilbert JR, Hussman JP, et al. Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants Molecular Autism. DOI: 10.1186/s13229-015-0034-z  0.16
2015 Beecham GW, Kunkle BW, Vardarajan B, Whitehead PL, Rolati S, Martin ER, Gilbert JR, Mayeux R, Haines JL, Pericak-Vance MA. O3-13-02: Whole-exome sequencing in early-onset Alzheimer disease cases identifies novel candidate genes Alzheimer's & Dementia. 11: P251-P251. DOI: 10.1016/J.Jalz.2015.07.310  0
2015 Cukier HN, Kunkle BW, Rolati S, Hamilton-Nelson KL, Kohli MA, Dombroski BA, Vardarajan BN, Whitehead PL, Booven DJV, Martin ER, Beecham GW, Farrer LA, Cuccaro ML, Vance JM, Mayeux R, ... Gilbert JR, et al. ABCA7 deletion associated with Alzheimer's disease in african americans Alzheimers & Dementia. 11. DOI: 10.1016/J.Jalz.2015.06.549  0
2014 Beecham GW, Hamilton K, Naj AC, Martin ER, Huentelman M, Myers AJ, Corneveaux JJ, Hardy J, Vonsattel JP, Younkin SG, Bennett DA, De Jager PL, Larson EB, Crane PK, Kamboh MI, ... ... Gilbert JR, et al. Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Plos Genetics. 10: e1004606. PMID 25188341 DOI: 10.1371/Journal.Pgen.1004606  0.16
2014 Hadley D, Wu ZL, Kao C, Kini A, Mohamed-Hadley A, Thomas K, Vazquez L, Qiu H, Mentch F, Pellegrino R, Kim C, Connolly J, Glessner J, Hakonarson H. The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism. Nature Communications. 5: 4074. PMID 24927284 DOI: 10.1038/Ncomms5074  0
2014 Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, ... Gilbert J, et al. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics. 94: 677-94. PMID 24768552 DOI: 10.1016/J.Ajhg.2014.03.018  0
2014 Cukier HN, Dueker ND, Slifer SH, Lee JM, Whitehead PL, Lalanne E, Leyva N, Konidari I, Gentry RC, Hulme WF, Booven DV, Mayo V, Hofmann NK, Schmidt MA, Martin ER, ... ... Gilbert JR, et al. Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders. Molecular Autism. 5: 1. PMID 24410847 DOI: 10.1186/2040-2392-5-1  0.16
2014 Kanoski SE, Alhadeff AL, Fortin SM, Gilbert JR, Grill HJ. Leptin signaling in the medial nucleus tractus solitarius reduces food seeking and willingness to work for food. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 39: 605-13. PMID 24002186 DOI: 10.1038/Npp.2013.235  0.04
2014 Carney RM, Kohli MA, Kunkle BW, Naj AC, Gilbert JR, Züchner S, Pericak-Vance MA. Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: 360-5. PMID 23727082 DOI: 10.1016/J.Jalz.2013.02.011  0.16
2014 Strnadová V, Buluc A, Chapman J, Gilbert JR, Gonzalez J, Jegelka S, Rokhsar D, Oliker L. Efficient and accurate clustering for large-scale genetic mapping Proceedings - 2014 Ieee International Conference On Bioinformatics and Biomedicine, Ieee Bibm 2014. 3-10. DOI: 10.1109/BIBM.2014.6999119  0.08
2014 Pericak-Vance M, Reitz C, Kunkle BW, Vardarajan BN, Kohli MA, Naj AC, Whitehead PL, Perry W, Martin E, Beecham G, Gilbert J, Farrer LA, Haines J, Schellenberg GD, Mayeux R. P2-131: WHOLE-EXOME SEQUENCING OF HISPANIC EARLY-ONSET ALZHEIMER DISEASE FAMILIES IDENTIFIES RARE VARIANTS IN MULTIPLE ALZHEIMER'S-RELATED GENES Alzheimer's & Dementia. 10: P518-P519. DOI: 10.1016/J.Jalz.2014.05.806  0
2014 Carney R, Kohli MA, Kunkle BW, Martin ER, Beecham GW, Gilbert JR, Pericak-Vance MA. P1-036: CLINICAL CHARACTERISTICS OF LATE ONSET ALZHEIMER DISEASE IN AN EXTENDED FAMILY WITH A MISSENSE VARIANT IN TTC3 Alzheimer's & Dementia. 10: P316-P316. DOI: 10.1016/J.Jalz.2014.05.271  0
2013 Murdock DG, Bradford Y, Schnetz-Boutaud N, Mayo P, Allen MJ, D'Aoust LN, Liang X, Mitchell SL, Zuchner S, Small GW, Gilbert JR, Pericak-Vance MA, Haines JL. KIAA1462, a coronary artery disease associated gene, is a candidate gene for late onset Alzheimer disease in APOE carriers. Plos One. 8: e82194. PMID 24349219 DOI: 10.1371/Journal.Pone.0082194  0.16
2013 Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, DeStafano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thorton-Wells TA, Jones N, Smith AV, Chouraki V, ... ... Gilbert JR, et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nature Genetics. 45: 1452-8. PMID 24162737 DOI: 10.1038/Ng.2802  0.01
2013 Nuytemans K, Bademci G, Kohli MM, Beecham GW, Wang L, Young JI, Nahab F, Martin ER, Gilbert JR, Benatar M, Haines JL, Scott WK, Züchner S, Pericak-Vance MA, Vance JM. C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease. Annals of Human Genetics. 77: 351-63. PMID 23845100 DOI: 10.1111/Ahg.12033  0.16
2013 Gilbert JR, Pillai AS, Horwitz B. Assessing crossmodal matching of abstract auditory and visual stimuli in posterior superior temporal sulcus with MEG. Brain and Cognition. 82: 161-70. PMID 23665947 DOI: 10.1016/J.Bandc.2013.03.004  0.01
2013 Hadjixenofontos A, Schmidt MA, Whitehead PL, Konidari I, Hedges DJ, Wright HH, Abramson RK, Menon R, Williams SM, Cuccaro ML, Haines JL, Gilbert JR, Pericak-Vance MA, Martin ER, McCauley JL. Evaluating mitochondrial DNA variation in autism spectrum disorders. Annals of Human Genetics. 77: 9-21. PMID 23130936 DOI: 10.1111/J.1469-1809.2012.00736.X  0.16
2013 Kohli MA, John-Williams K, Rajbhandary R, Naj A, Whitehead P, Hamilton K, Carney RM, Wright C, Crocco E, Gwirtzman HE, Lang R, Beecham G, Martin ER, Gilbert J, Benatar M, et al. Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians. Neurobiology of Aging. 34: 1519.e5-12. PMID 23107433 DOI: 10.1016/J.Neurobiolaging.2012.10.003  0
2013 Pillai AS, Gilbert JR, Horwitz B. Early sensory cortex is activated in the absence of explicit input during crossmodal item retrieval: evidence from MEG. Behavioural Brain Research. 238: 265-72. PMID 23084971 DOI: 10.1016/J.Bbr.2012.10.011  0.01
2013 Edwards DR, Gilbert JR, Hicks JE, Myers JL, Jiang L, Cummings AC, Guo S, Gallins PJ, Konidari I, Caywood L, Reinhart-Mercer L, Fuzzell D, Knebusch C, Laux R, Jackson CE, et al. Linkage and association of successful aging to the 6q25 region in large Amish kindreds. Age (Dordrecht, Netherlands). 35: 1467-77. PMID 22773346 DOI: 10.1007/S11357-012-9447-1  0.16
2013 Buluç A, Duriakova E, Fox A, Gilbert JR, Kamil S, Lugowski A, Oliker L, Williams S. High-productivity and high-performance analysis of filtered semantic graphs Proceedings - Ieee 27th International Parallel and Distributed Processing Symposium, Ipdps 2013. 237-248. DOI: 10.1109/IPDPS.2013.52  0.08
2013 Lugowski A, Kamil S, Buluç A, Williams S, Duriakova E, Oliker L, Fox A, Gilbert JR. Parallel processing of filtered queries in attributed semantic graphs Journal of Parallel and Distributed Computing. 79: 115-131. DOI: 10.1016/J.Jpdc.2014.08.010  0.08
2013 Humphries C, Whitehead PL, Mash D, Beecham G, Pericak-Vance M, Gilbert J. P1-053: Genome-wide analysis of DNA methylation differentiates late-onset Alzheimer's disease from dementia with Lewy bodies Alzheimer's & Dementia. 9: P171-P172. DOI: 10.1016/J.Jalz.2013.05.274  0
2013 Pericak-Vance M, Kunkle B, Kholi M, Naj A, Perry W, Hamilton K, Whitehead PL, Levin B, Carney R, Crocco E, Wright C, Beecham G, Martin E, Wang L, Gilbert J, et al. P3-021: Variant-domain mapping in confirmed late-onset Alzheimer disease (LOAD) loci identifies multiple genomic regions with potentially functional variants Alzheimer's & Dementia. 9: P557-P557. DOI: 10.1016/J.Jalz.2013.05.1090  0
2013 Humphries C, Gilbert J, Kohli M, Whitehead PL, Mash D, Beecham G, Pericak-Vance M. RNA transcription and editing in Alzheimer’s disease Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.04.474  0
2013 Kohli M, Kunkle B, Naj A, Carney RM, Hamilton-Nelson K, Rolati S, Whitehead PL, Gilbert J, Martin E, Beecham G, Wang L, Mayeux R, Haines J, Farrer L, Schellenberg G, et al. The identification of rare variants in late-onset Alzheimer’s disease using extended families Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.04.239  0
2013 Gilbert JR, McCaskill D, Fishman VN, Brzak K, Markham D, Bartels MJ, Winniford B, Bano Mohsin S, Godbey J, Akinbo O, Lewer P. Industrial applications of high-resolution GC/MS Comprehensive Analytical Chemistry. 61: 403-429. DOI: 10.1016/B978-0-444-62623-3.00017-4  0.2
2012 Whitcomb DC, LaRusch J, Krasinskas AM, Klei L, Smith JP, Brand RE, Neoptolemos JP, Lerch MM, Tector M, Sandhu BS, Guda NM, Orlichenko L, Alkaade S, Amann ST, et al. Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Nature Genetics. 44: 1349-54. PMID 23143602 DOI: 10.1038/Ng.2466  0
2012 Wang D, Gilbert JR, Cray JJ, Kubala AA, Shaw MA, Billiar TR, Cooper GM. Accelerated calvarial healing in mice lacking Toll-like receptor 4. Plos One. 7: e46945. PMID 23071670 DOI: 10.1371/journal.pone.0046945  0.04
2012 Cukier HN, Lee JM, Ma D, Young JI, Mayo V, Butler BL, Ramsook SS, Rantus JA, Abrams AJ, Whitehead PL, Wright HH, Abramson RK, Haines JL, Cuccaro ML, Pericak-Vance MA, ... Gilbert JR, et al. The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1. Autism Research : Official Journal of the International Society For Autism Research. 5: 385-97. PMID 23055267 DOI: 10.1002/Aur.1251  0.16
2012 Gilbert JR, Shapiro LR, Barnes GR. A peak-clustering method for MEG group analysis to minimise artefacts due to smoothness. Plos One. 7: e45084. PMID 23024795 DOI: 10.1371/Journal.Pone.0045084  0.01
2012 Cummings AC, Jiang L, Velez Edwards DR, McCauley JL, Laux R, McFarland LL, Fuzzell D, Knebusch C, Caywood L, Reinhart-Mercer L, Nations L, Gilbert JR, Konidari I, Tramontana M, Cuccaro ML, et al. Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene. Annals of Human Genetics. 76: 342-51. PMID 22881374 DOI: 10.1111/J.1469-1809.2012.00721.X  0.16
2012 Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, ... Gilbert J, et al. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics. 21: 4781-92. PMID 22843504 DOI: 10.1093/Hmg/Dds301  0
2012 Krupp DR, Xu PT, Thomas S, Dellinger A, Etchevers HC, Vekemans M, Gilbert JR, Speer MC, Ashley-Koch AE, Gregory SG. Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE). Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 683-92. PMID 22806986 DOI: 10.1002/Bdra.23040  0.16
2012 Griswold AJ, Ma D, Cukier HN, Nations LD, Schmidt MA, Chung RH, Jaworski JM, Salyakina D, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Martin ER, ... ... Gilbert JR, et al. Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Human Molecular Genetics. 21: 3513-23. PMID 22543975 DOI: 10.1093/Hmg/Dds164  0.16
2012 Hedges DJ, Hamilton-Nelson KL, Sacharow SJ, Nations L, Beecham GW, Kozhekbaeva ZM, Butler BL, Cukier HN, Whitehead PL, Ma D, Jaworski JM, Nathanson L, Lee JM, Hauser SL, Oksenberg JR, ... ... Gilbert JR, et al. Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci. Molecular Autism. 3: 2. PMID 22472195 DOI: 10.1186/2040-2392-3-2  0.16
2012 Velez Edwards DR, Tacconelli A, Wejse C, Hill PC, Morris GA, Edwards TL, Gilbert JR, Myers JL, Park YS, Stryjewski ME, Abbate E, Estevan R, Rabna P, Novelli G, Hamilton CD, et al. MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms. Plos One. 7: e32275. PMID 22384203 DOI: 10.1371/Journal.Pone.0032275  0.16
2012 Wang L, Hara K, Van Baaren JM, Price JC, Beecham GW, Gallins PJ, Whitehead PL, Wang G, Lu C, Slifer MA, Züchner S, Martin ER, Mash D, Haines JL, Pericak-Vance MA, ... Gilbert JR, et al. Vitamin D receptor and Alzheimer's disease: a genetic and functional study. Neurobiology of Aging. 33: 1844.e1-9. PMID 22306846 DOI: 10.1016/J.Neurobiolaging.2011.12.038  0.16
2012 Cuccaro ML, Tuchman RF, Hamilton KL, Wright HH, Abramson RK, Haines JL, Gilbert JR, Pericak-Vance M. Exploring the relationship between autism spectrum disorder and epilepsy using latent class cluster analysis. Journal of Autism and Developmental Disorders. 42: 1630-41. PMID 22105141 DOI: 10.1007/S10803-011-1402-Y  0.16
2012 Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, ... Gilbert J, et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics. 131: 565-79. PMID 21996756 DOI: 10.1007/S00439-011-1094-6  0
2012 Courtenay MD, Gilbert JR, Jiang L, Cummings AC, Gallins PJ, Caywood L, Reinhart-Mercer L, Fuzzell D, Knebusch C, Laux R, McCauley JL, Jackson CE, Pericak-Vance MA, Haines JL, Scott WK. Mitochondrial haplogroup X is associated with successful aging in the Amish. Human Genetics. 131: 201-8. PMID 21750925 DOI: 10.1007/S00439-011-1060-3  0.16
2012 Buluç A, Fox A, Gilbert JR, Kamil S, Lugowski A, Oliker L, Williams S. High-performance analysis of filtered semantic graphs Parallel Architectures and Compilation Techniques - Conference Proceedings, Pact. 463-464. DOI: 10.1145/2370816.2370897  0.08
2012 Buluç A, Gilbert JR. Parallel sparse matrix-matrix multiplication and indexing: Implementation and experiments Siam Journal On Scientific Computing. 34: C170-C191. DOI: 10.1137/110848244  0.08
2012 Friedland KD, Manning JP, Link JS, Gilbert JR, Gilbert AT, O'Connell AF. Variation in wind and piscivorous predator fields affecting the survival of Atlantic salmon, Salmo salar, in the Gulf of Maine Fisheries Management and Ecology. 19: 22-35. DOI: 10.1111/j.1365-2400.2011.00814.x  0.04
2012 Lugowski A, Buluç A, Gilbert JR, Reinhardt S. Scalable complex graph analysis with the knowledge discovery toolbox Icassp, Ieee International Conference On Acoustics, Speech and Signal Processing - Proceedings. 5345-5348. DOI: 10.1109/ICASSP.2012.6289128  0.08
2012 Pericak-Vance M, Zuchner S, Kohli M, John-Williams K, Naj A, Rajbhandary R, Whitehead PL, Hamilton-Nelson K, Carney R, Wright C, Crocco E, Gwirtzman H, Lang R, Beecham G, Martin E, ... Gilbert J, et al. Large repeat expansions in the C9ORF72 gene contribute to a spectrum of neurodegenerative disorders including Alzheimer's disease in Caucasians, but not African-Americans Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2013.08.277  0
2012 Humphries C, Kohli M, Whitehead PL, Plitnik T, John-Williams K, Mash D, Haines J, Pericak-Vance M, Gilbert J. Global assessment of non-coding RNA's regulation on altered transcription in the temporal pole of late-onset Alzheimer's disease patients Alzheimers & Dementia. 8: 254. DOI: 10.1016/J.Jalz.2012.05.677  0
2012 Zuchner S, Kohli M, Naj A, Hamilton K, Rajbhandary R, Plitnik T, John-Williams K, Whitehead PL, Gilbert J, Martin E, Beecham G, Haines J, Pericak-Vance M. Exome sequencing of extended late-onset Alzheimer's disease families identifies a variant in the TTC3 gene Alzheimers & Dementia. 8: 679. DOI: 10.1016/J.Jalz.2012.05.1839  0
2012 Lugowski A, Alber D, Buluç A, Gilbert JR, Reinhardt S, Teng Y, Waranis A. A flexible open-source toolbox for scalable complex graph analysis Proceedings of the 12th Siam International Conference On Data Mining, Sdm 2012. 930-941.  0.08
2011 Chung RH, Ma D, Wang K, Hedges DJ, Jaworski JM, Gilbert JR, Cuccaro ML, Wright HH, Abramson RK, Konidari I, Whitehead PL, Schellenberg GD, Hakonarson H, Haines JL, Pericak-Vance MA, et al. An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males. Molecular Autism. 2: 18. PMID 22050706 DOI: 10.1186/2040-2392-2-18  0.16
2011 Salyakina D, Cukier HN, Lee JM, Sacharow S, Nations LD, Ma D, Jaworski JM, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Haines JL, Gilbert JR, et al. Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk. Plos One. 6: e26049. PMID 22016809 DOI: 10.1371/Journal.Pone.0026049  0.16
2011 Edwards DR, Gilbert JR, Jiang L, Gallins PJ, Caywood L, Creason M, Fuzzell D, Knebusch C, Jackson CE, Pericak-Vance MA, Haines JL, Scott WK. Successful aging shows linkage to chromosomes 6, 7, and 14 in the Amish. Annals of Human Genetics. 75: 516-28. PMID 21668908 DOI: 10.1111/J.1469-1809.2011.00658.X  0.16
2011 Hedges DJ, Guettouche T, Yang S, Bademci G, Diaz A, Andersen A, Hulme WF, Linker S, Mehta A, Edwards YJ, Beecham GW, Martin ER, Pericak-Vance MA, Zuchner S, Vance JM, ... Gilbert JR, et al. Comparison of three targeted enrichment strategies on the SOLiD sequencing platform. Plos One. 6: e18595. PMID 21559511 DOI: 10.1371/Journal.Pone.0018595  0.16
2011 Kanoski SE, Hayes MR, Greenwald HS, Fortin SM, Gianessi CA, Gilbert JR, Grill HJ. Hippocampal leptin signaling reduces food intake and modulates food-related memory processing. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 36: 1859-70. PMID 21544068 DOI: 10.1038/Npp.2011.70  0.01
2011 Cukier HN, Salyakina D, Blankstein SF, Robinson JL, Sacharow S, Ma D, Wright HH, Abramson RK, Menon R, Williams SM, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 493-501. PMID 21480499 DOI: 10.1002/Ajmg.B.31188  0.16
2011 Naj AC, Jun G, Beecham GW, Wang LS, Vardarajan BN, Buros J, Gallins PJ, Buxbaum JD, Jarvik GP, Crane PK, Larson EB, Bird TD, Boeve BF, Graff-Radford NR, De Jager PL, ... ... Gilbert JR, et al. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nature Genetics. 43: 436-41. PMID 21460841 DOI: 10.1038/Ng.801  0.16
2011 Griswold AJ, Ma D, Sacharow SJ, Robinson JL, Jaworski JM, Wright HH, Abramson RK, Lybaek H, Øyen N, Cuccaro ML, Gilbert JR, Pericak-Vance MA. A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis. Autism Research : Official Journal of the International Society For Autism Research. 4: 221-7. PMID 21360829 DOI: 10.1002/Aur.186  0.16
2011 Morris GA, Edwards DR, Hill PC, Wejse C, Bisseye C, Olesen R, Edwards TL, Gilbert JR, Myers JL, Stryjewski ME, Abbate E, Estevan R, Hamilton CD, Tacconelli A, Novelli G, et al. Interleukin 12B (IL12B) genetic variation and pulmonary tuberculosis: a study of cohorts from The Gambia, Guinea-Bissau, United States and Argentina. Plos One. 6: e16656. PMID 21339808 DOI: 10.1371/Journal.Pone.0016656  0.16
2011 Hussman JP, Chung RH, Griswold AJ, Jaworski JM, Salyakina D, Ma D, Konidari I, Whitehead PL, Vance JM, Martin ER, Cuccaro ML, Gilbert JR, Haines JL, Pericak-Vance MA. A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism. Molecular Autism. 2: 1. PMID 21247446 DOI: 10.1186/2040-2392-2-1  0.16
2011 Buluç A, Gilbert JR. The combinatorial BLAS: Design, implementation, and applications International Journal of High Performance Computing Applications. 25: 496-509. DOI: 10.1177/1094342011403516  0.08
2011 Wood SA, Frasier TR, Mcleod BA, Gilbert JR, White BN, Bowen WD, Hammill MO, Waring GT, Brault S. The genetics of recolonization: An analysis of the stock structure of grey seals (Halichoerus grypus) in the Northwest Atlantic Canadian Journal of Zoology. 89: 490-497. DOI: 10.1139/Z11-012  0.04
2010 Salyakina D, Ma DQ, Jaworski JM, Konidari I, Whitehead PL, Henson R, Martinez D, Robinson JL, Sacharow S, Wright HH, Abramson RK, Gilbert JR, Cuccaro ML, Pericak-Vance MA. Variants in several genomic regions associated with asperger disorder. Autism Research : Official Journal of the International Society For Autism Research. 3: 303-10. PMID 21182207 DOI: 10.1002/Aur.158  0.16
2010 Naj AC, Beecham GW, Martin ER, Gallins PJ, Powell EH, Konidari I, Whitehead PL, Cai G, Haroutunian V, Scott WK, Vance JM, Slifer MA, Gwirtsman HE, Gilbert JR, Haines JL, et al. Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. Plos Genetics. 6: e1001130. PMID 20885792 DOI: 10.1371/Journal.Pgen.1001130  0.16
2010 Beecham GW, Martin ER, Gilbert JR, Haines JL, Pericak-Vance MA. APOE is not associated with Alzheimer disease: a cautionary tale of genotype imputation. Annals of Human Genetics. 74: 189-94. PMID 20529013 DOI: 10.1111/J.1469-1809.2010.00573.X  0.16
2010 Beecham GW, Naj AC, Gilbert JR, Haines JL, Buxbaum JD, Pericak-Vance MA. PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility. Psychiatric Genetics. 20: 321-4. PMID 20523261 DOI: 10.1097/Ypg.0B013E32833B635D  0.16
2010 Gilbert JR, Gotts SJ, Carver FW, Martin A. Object repetition leads to local increases in the temporal coordination of neural responses. Frontiers in Human Neuroscience. 4: 30. PMID 20463867 DOI: 10.3389/Fnhum.2010.00030  0.01
2010 Cukier HN, Rabionet R, Konidari I, Rayner-Evans MY, Baltos ML, Wright HH, Abramson RK, Martin ER, Cuccaro ML, Pericak-Vance MA, Gilbert JR. Novel variants identified in methyl-CpG-binding domain genes in autistic individuals. Neurogenetics. 11: 291-303. PMID 19921286 DOI: 10.1007/S10048-009-0228-7  0.16
2010 Velez DR, Wejse C, Stryjewski ME, Abbate E, Hulme WF, Myers JL, Estevan R, Patillo SG, Olesen R, Tacconelli A, Sirugo G, Gilbert JR, Hamilton CD, Scott WK. Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West Africans. Human Genetics. 127: 65-73. PMID 19771452 DOI: 10.1007/S00439-009-0741-7  0.16
2010 Ma DQ, Rabionet R, Konidari I, Jaworski J, Cukier HN, Wright HH, Abramson RK, Gilbert JR, Cuccaro ML, Pericak-Vance MA, Martin ER. Association and gene-gene interaction of SLC6A4 and ITGB3 in autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 477-83. PMID 19588468 DOI: 10.1002/Ajmg.B.31003  0.16
2010 Buluç A, Gilbert JR, Budak C. Solving path problems on the GPU Parallel Computing. 36: 241-253. DOI: 10.1016/j.parco.2009.12.002  0.08
2010 Beecham GW, Schnetz-Boutaud N, Bartlett J, Naj A, Gilbert J, Martin ER, Buxbaum J, Haines JL, Pericak-Vance MA. Copy number polymorphism at chromosome 19 locus associated with late-onset Alzheimer's disease Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.349  0
2009 Cukier HN, Skaar DA, Rayner-Evans MY, Konidari I, Whitehead PL, Jaworski JM, Cuccaro ML, Pericak-Vance MA, Gilbert JR. Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility. Autism Research : Official Journal of the International Society For Autism Research. 2: 258-66. PMID 19877165 DOI: 10.1002/Aur.96  0.16
2009 Young SA, Julka S, Bartley G, Gilbert JR, Wendelburg BM, Hung SC, Anderson WH, Yokoyama WH. Quantification of the sulfated cholecystokinin CCK-8 in hamster plasma using immunoprecipitation liquid chromatography-mass spectrometry/mass spectrometry. Analytical Chemistry. 81: 9120-8. PMID 19799376 DOI: 10.1021/ac9018318  0.2
2009 Velez DR, Hulme WF, Myers JL, Stryjewski ME, Abbate E, Estevan R, Patillo SG, Gilbert JR, Hamilton CD, Scott WK. Association of SLC11A1 with tuberculosis and interactions with NOS2A and TLR2 in African-Americans and Caucasians. The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease. 13: 1068-76. PMID 19723394  0.16
2009 Schnetz-Boutaud NC, Anderson BM, Brown KD, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL. Examination of tetrahydrobiopterin pathway genes in autism. Genes, Brain, and Behavior. 8: 753-7. PMID 19674121 DOI: 10.1111/J.1601-183X.2009.00521.X  0.16
2009 Velez DR, Hulme WF, Myers JL, Weinberg JB, Levesque MC, Stryjewski ME, Abbate E, Estevan R, Patillo SG, Gilbert JR, Hamilton CD, Scott WK. NOS2A, TLR4, and IFNGR1 interactions influence pulmonary tuberculosis susceptibility in African-Americans. Human Genetics. 126: 643-53. PMID 19575238 DOI: 10.1007/S00439-009-0713-Y  0.16
2009 Ma D, Salyakina D, Jaworski JM, Konidari I, Whitehead PL, Andersen AN, Hoffman JD, Slifer SH, Hedges DJ, Cukier HN, Griswold AJ, McCauley JL, Beecham GW, Wright HH, Abramson RK, ... ... Gilbert JR, et al. A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. Annals of Human Genetics. 73: 263-73. PMID 19456320 DOI: 10.1111/J.1469-1809.2009.00523.X  0.16
2009 Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, ... ... Gilbert JR, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 459: 528-33. PMID 19404256 DOI: 10.1038/Nature07999  0.16
2009 Gilbert JR, Adams CS, Shapiro IM, Hickok NJ. A novel short hairpin RNA (shRNA) expression system promotes Sox9-dependent gene silencing. Plasmid. 62: 50-5. PMID 19389425 DOI: 10.1016/J.Plasmid.2009.04.001  0.08
2009 Slifer MA, Martin ER, Gilbert JR, Haines JL, Pericak-Vance MA. Resolving the relationship between ApolipoproteinE and depression. Neuroscience Letters. 455: 116-9. PMID 19368858 DOI: 10.1016/J.Neulet.2009.03.007  0.16
2009 Lewer P, Hahn DR, Karr LL, Duebelbeis DO, Gilbert JR, Crouse GD, Worden T, Sparks TC, Edwards PM, Graupner PR. Discovery of the butenyl-spinosyn insecticides: novel macrolides from the new bacterial strain Saccharopolyspora pogona. Bioorganic & Medicinal Chemistry. 17: 4185-96. PMID 19324553 DOI: 10.1016/J.Bmc.2009.02.035  0.2
2009 Hahn DR, Graupner PR, Chapin E, Gray J, Heim D, Gilbert JR, Gerwick BC. Albucidin: a novel bleaching herbicide from Streptomyces albus subsp. chlorinus NRRL B-24108. The Journal of Antibiotics. 62: 191-4. PMID 19247393 DOI: 10.1038/ja.2009.11  0.2
2009 Liang X, Slifer M, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Gilbert JR, Pericak-Vance MA, Haines JL. Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10. Human Mutation. 30: 463-71. PMID 19241460 DOI: 10.1002/Humu.20953  0.16
2009 Anderson BM, Schnetz-Boutaud NC, Bartlett J, Wotawa AM, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL. Examination of association of genes in the serotonin system to autism. Neurogenetics. 10: 209-16. PMID 19184136 DOI: 10.1007/S10048-009-0171-7  0.16
2009 Cukier HN, Pericak-Vance MA, Gilbert JR, Hedges DJ. Sample degradation leads to false-positive copy number variation calls in multiplex real-time polymerase chain reaction assays. Analytical Biochemistry. 386: 288-90. PMID 19121619 DOI: 10.1016/J.Ab.2008.11.040  0.16
2009 Beecham GW, Martin ER, Li YJ, Slifer MA, Gilbert JR, Haines JL, Pericak-Vance MA. Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. American Journal of Human Genetics. 84: 35-43. PMID 19118814 DOI: 10.1016/J.Ajhg.2008.12.008  0.16
2009 Edwards TL, Pericak-Vance M, Gilbert JR, Haines JL, Martin ER, Ritchie MD. An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 721-35. PMID 19105203 DOI: 10.1002/Ajmg.B.30899  0.16
2009 Buluç A, Fineman JT, Frigo M, Gilbert JR, Leiserson CE. Parallel sparse matrix-vector and matrix-transpose-vector multiplication using compressed sparse blocks Annual Acm Symposium On Parallelism in Algorithms and Architectures. 233-244. DOI: 10.1145/1583991.1584053  0.08
2009 Naj AC, Beecham GW, Slifer MA, Martin ER, Gallins PJ, Konidari I, Whitehead PL, Cai G, Kajiwara Y, Haroutunian V, Gwirtsman HE, Gilbert JR, Haines JL, Buxbaum JD, Pericak-Vance MA. Genome-wide association study validates associations in APOE, VDR, SORL1, WWC1, and ELAVL4 and identifies novel candidate genes for late-onset Alzheimer's disease Alzheimers & Dementia. 5. DOI: 10.1016/J.Jalz.2009.05.519  0
2009 Beecham GW, Naj AC, Cai G, Kajiwara Y, Haroutunian V, Konidari I, Gallins P, Whitehead P, Gilbert JR, Slifer MA, Gwirstman H, Martin ER, Buxbaum J, Haines JL, Pericak-Vance MA. GRB-associated binding protein 2 (GAB2) interacts with APOE to alter risk of late-onset Alzheimer's disease Alzheimers & Dementia. 5: 111. DOI: 10.1016/J.Jalz.2009.05.348  0
2009 Karpinski S, Belding EM, Almeroth KC, Gilbert JR. Linear representation of network traffic: With special application to wireless workload generation Mobile Networks and Applications. 14: 368-386. DOI: 10.1007/S11036-008-0110-0  0.08
2008 Anderson BM, Schnetz-Boutaud N, Bartlett J, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL. Examination of association to autism of common genetic variationin genes related to dopamine. Autism Research : Official Journal of the International Society For Autism Research. 1: 364-9. PMID 19360691 DOI: 10.1002/Aur.55  0.16
2008 Stamm DS, Powell CM, Stajich JM, Zismann VL, Stephan DA, Chesnut B, Aylsworth AS, Kahler SG, Deak KL, Gilbert JR, Speer MC. Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1. Neurology. 71: 1764-9. PMID 18843099 DOI: 10.1212/01.Wnl.0000325060.16532.40  0.16
2008 Züchner S, Gilbert JR, Martin ER, Leon-Guerrero CR, Xu PT, Browning C, Bronson PG, Whitehead P, Schmechel DE, Haines JL, Pericak-Vance MA. Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3. Annals of Human Genetics. 72: 725-31. PMID 18761660 DOI: 10.1111/J.1469-1809.2008.00474.X  0.16
2008 Stamm DS, Siegel DG, Mehltretter L, Connelly JJ, Trott A, Ellis N, Zismann V, Stephan DA, George TM, Vekemans M, Ashley-Koch A, Gilbert JR, Gregory SG, Speer MC. Refinement of 2q and 7p loci in a large multiplex NTD family. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 441-52. PMID 18452155 DOI: 10.1002/Bdra.20462  0.16
2008 Liang X, Schnetz-Boutaud N, Bartlett J, Allen MJ, Gwirtsman H, Schmechel DE, Carney RM, Gilbert JR, Pericak-Vance MA, Haines JL. No association between SNP rs498055 on chromosome 10 and late-onset Alzheimer disease in multiple datasets. Annals of Human Genetics. 72: 141-4. PMID 17725684 DOI: 10.1111/J.1469-1809.2007.00394.X  0.16
2008 Slifer MA, Beecham GW, Martin ER, Wang G, Gilbert JR, Haines JL, Vance J, Pericak-Vance MA. O2-06-02: A genetic susceptibility locus for depression of Alzheimer's disease and Parkinson's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.350  0
2008 Hara K, Gilbert J, Gallins P, Whitehead P, Beecham G, Slifer M, Martin E, Haines J, Pericak-Vance M. P3-228: Genetic association of vitamin D receptor gene on chromosome 12q with late-onset Alzheimer's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1795  0
2008 Gilbert JR, Beecham G, Gallins P, Slifer M, Martin ER, Haines J, Pericak-Vance MA. P3-223: Genome-wide association analysis of the age-at-onset for individuals with Alzheimer's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1790  0
2008 Beecham GW, Slifer MA, Martin ER, Li Y, Carney RM, Gilbert JR, Haines JL, Pericak-Vance MA. P3-200: Genomic convergence of late-onset Alzheimer's disease candidate genes Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1766  0
2007 Snipes CE, Duebelbeis DO, Olson M, Hahn DR, Dent WH, Gilbert JR, Werk TL, Davis GE, Lee-Lu R, Graupner PR. The ansacarbamitocins: polar ansamitocin derivatives. Journal of Natural Products. 70: 1578-81. PMID 17892263 DOI: 10.1021/np070275t  0.2
2007 Xu PT, Li YJ, Qin XJ, Kroner C, Green-Odlum A, Xu H, Wang TY, Schmechel DE, Hulette CM, Ervin J, Hauser M, Haines J, Pericak-Vance MA, Gilbert JR. A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease. Molecular and Cellular Neurosciences. 36: 313-31. PMID 17822919 DOI: 10.1016/J.Mcn.2007.06.009  0.16
2007 Cuccaro ML, Brinkley J, Abramson RK, Hall A, Wright HH, Hussman JP, Gilbert JR, Pericak-Vance MA. Autism in African American families: clinical-phenotypic findings. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 1022-6. PMID 17671983 DOI: 10.1002/Ajmg.B.30535  0.16
2007 Ashley-Koch AE, Jaworski J, Ma de Q, Mei H, Ritchie MD, Skaar DA, Robert Delong G, Worley G, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA. Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk. Psychiatric Genetics. 17: 221-6. PMID 17621165 DOI: 10.1097/Ypg.0B013E32809C2F75  0.16
2007 Liang X, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Schmechel D, Carney R, Gilbert JR, Pericak-Vance MA, Haines JL. Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease. Human Mutation. 28: 1065-73. PMID 17573676 DOI: 10.1002/Humu.20567  0.16
2007 Han F, Gilbert JR, Harrison G, Adams CS, Freeman T, Tao Z, Zaka R, Liang H, Williams C, Tuan RS, Norton PA, Hickok NJ. Transforming growth factor-beta1 regulates fibronectin isoform expression and splicing factor SRp40 expression during ATDC5 chondrogenic maturation. Experimental Cell Research. 313: 1518-32. PMID 17391668 DOI: 10.1016/J.Yexcr.2007.01.028  0.08
2007 Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, ... ... Gilbert JR, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985  0.16
2007 Scott WK, Schmidt S, Hauser MA, Gallins P, Schnetz-Boutaud N, Spencer KL, Gilbert JR, Agarwal A, Postel EA, Haines JL, Pericak-Vance MA. Independent effects of complement factor H Y402H polymorphism and cigarette smoking on risk of age-related macular degeneration. Ophthalmology. 114: 1151-6. PMID 17241667 DOI: 10.1016/J.Ophtha.2006.08.054  0.16
2007 Deak KL, Lemmers RJ, Stajich JM, Klooster R, Tawil R, Frants RR, Speer MC, van der Maarel SM, Gilbert JR. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4. Neurology. 68: 578-82. PMID 17229919 DOI: 10.1212/01.Wnl.0000254991.21818.F3  0.16
2007 Brinkley J, Nations L, Abramson RK, Hall A, Wright HH, Gabriels R, Gilbert JR, Pericak-Vance MA, Cuccaro ML. Factor analysis of the aberrant behavior checklist in individuals with autism spectrum disorders. Journal of Autism and Developmental Disorders. 37: 1949-59. PMID 17186368 DOI: 10.1007/S10803-006-0327-3  0.16
2007 Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14. Molecular Psychiatry. 12: 376-84. PMID 17179998 DOI: 10.1038/Sj.Mp.4001927  0.16
2007 Liang X, Schnetz-Boutaud N, Bartlett J, Anderson BM, Gwirtsman H, Schmechel D, Carney R, Gilbert JR, Pericak-Vance MA, Haines JL. Association analysis of genetic polymorphisms in the CDC2 gene with late-onset Alzheimer disease. Dementia and Geriatric Cognitive Disorders. 23: 126-32. PMID 17159347 DOI: 10.1159/000097857  0.16
2006 Li YJ, Xu P, Qin X, Schmechel DE, Hulette CM, Haines JL, Pericak-Vance MA, Gilbert JR. A comparative analysis of the information content in long and short SAGE libraries. Bmc Bioinformatics. 7: 504. PMID 17109755 DOI: 10.1186/1471-2105-7-504  0.16
2006 Boyles AL, Enterline DS, Hammock PH, Siegel DG, Slifer SH, Mehltretter L, Gilbert JR, Hu-Lince D, Stephan D, Batzdorf U, Benzel E, Ellenbogen R, Green BA, Kula R, Menezes A, et al. Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15. American Journal of Medical Genetics. Part A. 140: 2776-85. PMID 17103432 DOI: 10.1002/Ajmg.A.31546  0.16
2006 Lewer P, Graupner PR, Hahn DR, Karr LL, Duebelbeis DO, Lira JM, Anzeveno PB, Fields SC, Gilbert JR, Pearce C. Discovery, synthesis, and insecticidal activity of cycloaspeptide E. Journal of Natural Products. 69: 1506-10. PMID 17067173 DOI: 10.1021/np060219c  0.01
2006 Boyles AL, Billups AV, Deak KL, Siegel DG, Mehltretter L, Slifer SH, Bassuk AG, Kessler JA, Reed MC, Nijhout HF, George TM, Enterline DS, Gilbert JR, Speer MC. Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions. Environmental Health Perspectives. 114: 1547-52. PMID 17035141 DOI: 10.1289/Ehp.9166  0.16
2006 Stamm DS, Rampersaud E, Slifer SH, Mehltretter L, Siegel DG, Xie J, Hu-Lince D, Craig DW, Stephan DA, George TM, Gilbert JR, Speer MC. High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35. Birth Defects Research. Part a, Clinical and Molecular Teratology. 76: 499-505. PMID 16933213 DOI: 10.1002/Bdra.20272  0.16
2006 Lin PI, Martin ER, Bronson PG, Browning-Large C, Small GW, Schmechel DE, Welsh-Bohmer KA, Haines JL, Gilbert JR, Pericak-Vance MA. Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease. Neurology. 67: 64-8. PMID 16832079 DOI: 10.1212/01.Wnl.0000223438.90113.4E  0.16
2006 Collins AL, Ma D, Whitehead PL, Martin ER, Wright HH, Abramson RK, Hussman JP, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Investigation of autism and GABA receptor subunit genes in multiple ethnic groups. Neurogenetics. 7: 167-74. PMID 16770606 DOI: 10.1007/S10048-006-0045-1  0.16
2006 Lin PI, Martin ER, Browning-Large CA, Schmechel DE, Welsh-Bohmer KA, Doraiswamy PM, Gilbert JR, Haines JL, Pericak-Vance MA. Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis. Neurogenetics. 7: 157-65. PMID 16770605 DOI: 10.1007/S10048-006-0047-Z  0.16
2006 Ashley-Koch AE, Mei H, Jaworski J, Ma DQ, Ritchie MD, Menold MM, Delong GR, Abramson RK, Wright HH, Hussman JP, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA. An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder. Annals of Human Genetics. 70: 281-92. PMID 16674551 DOI: 10.1111/J.1469-1809.2006.00253.X  0.16
2006 Rabionet R, McCauley JL, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, DeLong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Lack of association between autism and SLC25A12. The American Journal of Psychiatry. 163: 929-31. PMID 16648338 DOI: 10.1176/Ajp.2006.163.5.929  0.16
2006 Slifer MA, Martin ER, Bronson PG, Browning-Large C, Doraiswamy PM, Welsh-Bohmer KA, Gilbert JR, Haines JL, Pericak-Vance MA. Lack of association between UBQLN1 and Alzheimer disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 208-13. PMID 16526030 DOI: 10.1002/Ajmg.B.30298  0.16
2006 Gao Y, Fencil KJ, Xu X, Schwedler DA, Gilbert JR, Herman RA. Purification and characterization of a chimeric Cry1F delta-endotoxin expressed in transgenic cotton plants. Journal of Agricultural and Food Chemistry. 54: 829-35. PMID 16448190 DOI: 10.1021/jf0523869  0.2
2006 Qian Z, Haessler M, Lemos JA, Arsenault JR, Aguirre JE, Gilbert JR, Bowler RP, Park F. Targeting vascular injury using Hantavirus-pseudotyped lentiviral vectors. Molecular Therapy : the Journal of the American Society of Gene Therapy. 13: 694-704. PMID 16431160 DOI: 10.1016/J.Ymthe.2005.11.016  0.04
2006 Haines JL, Schnetz-Boutaud N, Schmidt S, Scott WK, Agarwal A, Postel EA, Olson L, Kenealy SJ, Hauser M, Gilbert JR, Pericak-Vance MA. Functional candidate genes in age-related macular degeneration: significant association with VEGF, VLDLR, and LRP6. Investigative Ophthalmology & Visual Science. 47: 329-35. PMID 16384981 DOI: 10.1167/Iovs.05-0116  0.16
2006 Liang X, Schnetz-Boutaud N, Kenealy SJ, Jiang L, Bartlett J, Lynch B, Gaskell PC, Gwirtsman H, McFarland L, Bembe ML, Bronson P, Gilbert JR, Martin ER, Pericak-Vance MA, Haines JL. Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus. Molecular Psychiatry. 11: 280-5. PMID 16222332 DOI: 10.1038/Sj.Mp.4001766  0.16
2006 Xu PT, Li YJ, Qin XJ, Scherzer CR, Xu H, Schmechel DE, Hulette CM, Ervin J, Gullans SR, Haines J, Pericak-Vance MA, Gilbert JR. Differences in apolipoprotein E3/3 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease. Neurobiology of Disease. 21: 256-75. PMID 16198584 DOI: 10.1016/J.Nbd.2005.07.004  0.16
2006 Zuchner S, Xu P, Browning C, Bronson PG, Martin ER, Gilbert JR, Haines JL, Pericak-Vance MA. P1-362: Genetic evaluation of the Alzheimer’s disease locus on chromosome 9p21.3 Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.740  0
2006 Bronson PG, Wall NN, Haines JL, Schmechel DE, Gilbert JR, Pericak-Vance MA, Martin ER. P1-345: Evidence for association between late-onset Alzheimer's disease and MTHFR on chromosome 1 Alzheimer's & Dementia. 2: S198-S198. DOI: 10.1016/J.Jalz.2006.05.723  0
2006 Slifer MA, Gilbert JR, Lin P, Liang X, Haines JL, Pericak-Vance MA. P1-330: Large scale candidate gene association studies in Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.708  0
2006 Schnetz-Boutaud N, Liang X, Martin ER, Anderson BM, Zuchner S, Gilbert JR, Pericak-Vance MA, Haines JL. P1-313: Examination of the effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.691  0
2005 Schmidt S, Haines JL, Postel EA, Agarwal A, Kwan SY, Gilbert JR, Pericak-Vance MA, Scott WK. Joint effects of smoking history and APOE genotypes in age-related macular degeneration. Molecular Vision. 11: 941-9. PMID 16288198  0.16
2005 Deak KL, Dickerson ME, Linney E, Enterline DS, George TM, Melvin EC, Graham FL, Siegel DG, Hammock P, Mehltretter L, Bassuk AG, Kessler JA, Gilbert JR, Speer MC. Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2. Birth Defects Research. Part a, Clinical and Molecular Teratology. 73: 868-75. PMID 16237707 DOI: 10.1002/Bdra.20183  0.16
2005 Martin ER, Bronson PG, Li YJ, Wall N, Chung RH, Schmechel DE, Small G, Xu PT, Bartlett J, Schnetz-Boutaud N, Haines JL, Gilbert JR, Pericak-Vance MA. Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease. Journal of Medical Genetics. 42: 787-92. PMID 16199552 DOI: 10.1136/Jmg.2004.029553  0.16
2005 Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA. Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism. American Journal of Human Genetics. 77: 377-88. PMID 16080114 DOI: 10.1086/433195  0.16
2005 Detrait ER, George TM, Etchevers HC, Gilbert JR, Vekemans M, Speer MC. Human neural tube defects: developmental biology, epidemiology, and genetics. Neurotoxicology and Teratology. 27: 515-24. PMID 15939212 DOI: 10.1016/J.Ntt.2004.12.007  0.16
2005 Deak KL, Boyles AL, Etchevers HC, Melvin EC, Siegel DG, Graham FL, Slifer SH, Enterline DS, George TM, Vekemans M, McClay D, Bassuk AG, Kessler JA, Linney E, Gilbert JR, et al. SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects. Human Genetics. 117: 133-42. PMID 15883837 DOI: 10.1007/S00439-005-1299-7  0.16
2005 Postel EA, Agarwal A, Schmidt S, Fan YT, Scott WK, Gilbert JR, Haines JL, Pericak-Vance MA. Comparing age-related macular degeneration phenotype in probands from singleton and multiplex families. American Journal of Ophthalmology. 139: 820-5. PMID 15860286 DOI: 10.1016/J.Ajo.2004.12.029  0.16
2005 Rampersaud E, Bassuk AG, Enterline DS, George TM, Siegel DG, Melvin EC, Aben J, Allen J, Aylsworth A, Brei T, Bodurtha J, Buran C, Floyd LE, Hammock P, Iskandar B, ... ... Gilbert JR, et al. Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10. Journal of Medical Genetics. 42: 940-6. PMID 15831595 DOI: 10.1136/Jmg.2005.031658  0.16
2005 Bastress KL, Stajich JM, Speer MC, Gilbert JR. The genes encoding for D4Z4 binding proteins HMGB2, YY1, NCL, and MYOD1 are excluded as candidate genes for FSHD1B. Neuromuscular Disorders : Nmd. 15: 316-20. PMID 15792872 DOI: 10.1016/J.Nmd.2004.12.006  0.16
2005 Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA. Complement factor H variant increases the risk of age-related macular degeneration. Science (New York, N.Y.). 308: 419-21. PMID 15761120 DOI: 10.1126/Science.1110359  0.16
2005 Ma DQ, Jaworski J, Menold MM, Donnelly S, Abramson RK, Wright HH, Delong GR, Gilbert JR, Pericak-Vance MA, Cuccaro ML. Ordered-subset analysis of savant skills in autism for 15q11-q13. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 135: 38-41. PMID 15756693 DOI: 10.1002/Ajmg.B.30166  0.16
2005 Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA. Analysis of the RELN gene as a genetic risk factor for autism. Molecular Psychiatry. 10: 563-71. PMID 15558079 DOI: 10.1038/Sj.Mp.4001614  0.16
2004 Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes. Neuroscience Letters. 372: 209-14. PMID 15542242 DOI: 10.1016/J.Neulet.2004.09.037  0.16
2004 Nicodemus KK, Stenger JE, Schmechel DE, Welsh-Bohmer KA, Saunders AM, Roses AD, Gilbert JR, Vance JM, Haines JL, Pericak-Vance MA, Martin ER. Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease. Neurogenetics. 5: 201-8. PMID 15455263 DOI: 10.1007/S10048-004-0189-9  0.16
2004 Benz LP, Swift FE, Graham FL, Enterline DS, Melvin EC, Hammock P, Gilbert JR, Speer MC, Bassuk AG, Kessler JA, George TM. TERC is not a major gene in human neural tube defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 531-3. PMID 15329831 DOI: 10.1002/Bdra.20057  0.16
2004 Schmidt S, Scott WK, Postel EA, Agarwal A, Hauser ER, De La Paz MA, Gilbert JR, Weeks DE, Gorin MB, Haines JL, Pericak-Vance MA. Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12. Bmc Genetics. 5: 18. PMID 15238159 DOI: 10.1186/1471-2156-5-18  0.16
2004 van der Walt JM, Dementieva YA, Martin ER, Scott WK, Nicodemus KK, Kroner CC, Welsh-Bohmer KA, Saunders AM, Roses AD, Small GW, Schmechel DE, Murali Doraiswamy P, Gilbert JR, Haines JL, Vance JM, et al. Analysis of European mitochondrial haplogroups with Alzheimer disease risk. Neuroscience Letters. 365: 28-32. PMID 15234467 DOI: 10.1016/J.Neulet.2004.04.051  0.16
2004 Raiford KL, Shao Y, Allen IC, Martin ER, Menold MM, Wright HH, Abramson RK, Worley G, DeLong GR, Vance JM, Cuccaro ML, Gilbert JR, Pericak-Vance MA. No association between the APOE gene and autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 125: 57-60. PMID 14755445 DOI: 10.1002/Ajmg.B.20104  0.16
2004 Li Y. Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease Human Molecular Genetics. 13: 573-573. DOI: 10.1093/Hmg/Ddh059  0
2004 Quan H, Haines JL, Sanchez-Boutard N, Small G, Roses A, Schmechel D, Welsh-Bohmer K, Xu P, Li Y, Gilbert JR, Vance JM, Pericak-Vance MA. P4-138 Genomic convergence on chromosome 12 in Alzheimer's disease Neurobiology of Aging. 25: S514. DOI: 10.1016/S0197-4580(04)81696-8  0
2004 Gilbert JR, Xu P, Li Y, Qin X, Schmechel D, Hulette C, McLaurin A, Scherzer C, Gullans SR, Haines JL, Pericak-Vance MA. P4-103 APOE allele specific gene expression in Alzheimer's and control hippocampus Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81661-0  0
2004 Pericak-Vance MA, Bronson P, Martin ER, Browning C, Rayner M, Xu P, Small GW, Roses AD, Schmechel DE, Doraiswamy PM, Welsh-Bohmer KA, Haines JL, Gilbert JR. P4-080 Genetic studies of Alzheimer disease on chromosome 9P Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81638-5  0
2004 Xu P, Hulette C, Hauser M, Schmechel DE, Pericak-Vance MA, Gilbert JR. O1-03-06 Transcription analysis of APOE specific hippocampus in Alzheimer's disease (AD) using serial analysis of gene expression (SAGE) and long-SAGE Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80049-6  0
2003 Li YJ, Oliveira SA, Xu P, Martin ER, Stenger JE, Scherzer CR, Hauser MA, Scott WK, Small GW, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, ... ... Gilbert JR, et al. Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease. Human Molecular Genetics. 12: 3259-67. PMID 14570706 DOI: 10.1093/Hmg/Ddg357  0.16
2003 Scott WK, Hauser ER, Schmechel DE, Welsh-Bohmer KA, Small GW, Roses AD, Saunders AM, Gilbert JR, Vance JM, Haines JL, Pericak-Vance MA. Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22. American Journal of Human Genetics. 73: 1041-51. PMID 14564669 DOI: 10.1086/379083  0.16
2003 Martin ER, Bass MP, Gilbert JR, Pericak-Vance MA, Hauser ER. Genotype-based association test for general pedigrees: the genotype-PDT. Genetic Epidemiology. 25: 203-13. PMID 14557988 DOI: 10.1002/Gepi.10258  0.16
2003 Oliveira SA, Martin ER, Scott WK, Nicodemus KK, Small GW, Schmechel DE, Doraiswamy PM, Roses AD, Saunders AM, Gilbert JR, Haines JL, Vance JM, Pericak-Vance MA. The Q7R Saitohin gene polymorphism is not associated with Alzheimer disease. Neuroscience Letters. 347: 143-6. PMID 12875906 DOI: 10.1016/S0304-3940(03)00670-0  0.16
2003 Schmidt S, Postel EA, Agarwal A, Allen IC, Walters SN, De la Paz MA, Scott WK, Haines JL, Pericak-Vance MA, Gilbert JR. Detailed analysis of allelic variation in the ABCA4 gene in age-related maculopathy. Investigative Ophthalmology & Visual Science. 44: 2868-75. PMID 12824224 DOI: 10.1167/Iovs.02-0957  0.16
2003 Shao Y, Cuccaro ML, Hauser ER, Raiford KL, Menold MM, Wolpert CM, Ravan SA, Elston L, Decena K, Donnelly SL, Abramson RK, Wright HH, DeLong GR, Gilbert JR, Pericak-Vance MA. Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes. American Journal of Human Genetics. 72: 539-48. PMID 12567325 DOI: 10.1086/367846  0.16
2002 Speer MC, Melvin EC, Viles KD, Bauer KA, Rampersaud E, Drake C, George TM, Enterline DS, Mackey JF, Worley G, Gilbert JR, Nye JS. T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families. American Journal of Medical Genetics. 110: 215-8. PMID 12116228 DOI: 10.1002/Ajmg.10436  0.16
2002 Teter B, Xu PT, Gilbert JR, Roses AD, Galasko D, Cole GM. Defective neuronal sprouting by human apolipoprotein E4 is a gain-of-negative function. Journal of Neuroscience Research. 68: 331-6. PMID 12111863 DOI: 10.1002/jnr.10221  0.16
2002 Li YJ, Scott WK, Hedges DJ, Zhang F, Gaskell PC, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Jankovic J, Allen FA, Goetz CG, ... ... Gilbert JR, et al. Age at onset in two common neurodegenerative diseases is genetically controlled. American Journal of Human Genetics. 70: 985-93. PMID 11875758 DOI: 10.1086/339815  0.16
2002 Shao Y, Raiford KL, Wolpert CM, Cope HA, Ravan SA, Ashley-Koch AA, Abramson RK, Wright HH, DeLong RG, Gilbert JR, Cuccaro ML, Pericak-Vance MA. Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder. American Journal of Human Genetics. 70: 1058-61. PMID 11875756 DOI: 10.1086/339765  0.16
2002 McCoy PA, Shao Y, Wolpert CM, Donnelly SL, Ashley-Koch A, Abel HL, Ravan SA, Abramson RK, Wright HH, DeLong GR, Cuccaro ML, Gilbert JR, Pericak-Vance MA. No association between the WNT2 gene and autistic disorder. American Journal of Medical Genetics. 114: 106-9. PMID 11840514 DOI: 10.1002/Ajmg.10182  0.16
2002 Shao Y, Wolpert CM, Raiford KL, Menold MM, Donnelly SL, Ravan SA, Bass MP, McClain C, von Wendt L, Vance JM, Abramson RH, Wright HH, Ashley-Koch A, Gilbert JR, DeLong RG, et al. Genomic screen and follow-up analysis for autistic disorder. American Journal of Medical Genetics. 114: 99-105. PMID 11840513 DOI: 10.1002/Ajmg.10153  0.16
2002 Baxter RV, Ben Othmane K, Rochelle JM, Stajich JE, Hulette C, Dew-Knight S, Hentati F, Ben Hamida M, Bel S, Stenger JE, Gilbert JR, Pericak-Vance MA, Vance JM. Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21. Nature Genetics. 30: 21-2. PMID 11743579 DOI: 10.1038/Ng796  0.16
2001 Gilbert JR, Vance JM. Isolation of genomic DNA from mammalian cells. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Appendix 3B. PMID 18428220 DOI: 10.1002/0471142905.Hga03Bs19  0.16
2001 Menold MM, Shao Y, Wolpert CM, Donnelly SL, Raiford KL, Martin ER, Ravan SA, Abramson RK, Wright HH, Delong GR, Cuccaro ML, Pericak-Vance MA, Gilbert JR. Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder. Journal of Neurogenetics. 15: 245-59. PMID 12092907 DOI: 10.3109/01677060109167380  0.16
2001 Nurmi EL, Bradford Y, Chen Y, Hall J, Arnone B, Gardiner MB, Hutcheson HB, Gilbert JR, Pericak-Vance MA, Copeland-Yates SA, Michaelis RC, Wassink TH, Santangelo SL, Sheffield VC, Piven J, et al. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. Genomics. 77: 105-13. PMID 11543639 DOI: 10.1006/Geno.2001.6617  0.16
2001 Wolpert CM, Donnelly SL, Cuccaro ML, Hedges DJ, Poole CP, Wright HH, Gilbert JR, Pericak-Vance MA. De novo partial duplication of chromosome 7p in a male with autistic disorder. American Journal of Medical Genetics. 105: 222-5. PMID 11353439 DOI: 10.1002/Ajmg.1258  0.16
2000 Bass MP, Menold MM, Wolpert CM, Donnelly SL, Ravan SA, Hauser ER, Maddox LO, Vance JM, Abramson RK, Wright HH, Gilbert JR, Cuccaro ML, DeLong GR, Pericak-Vance MA. Genetic studies in autistic disorder and chromosome 15. Neurogenetics. 2: 219-26. PMID 10983717 DOI: 10.1007/S100489900081  0.16
2000 Rosenberg CK, Pericak-Vance MA, Saunders AM, Gilbert JR, Gaskell PC, Hulette CM. Lewy body and Alzheimer pathology in a family with the amyloid-beta precursor protein APP717 gene mutation. Acta Neuropathologica. 100: 145-52. PMID 10963361 DOI: 10.1007/S004019900155  0.16
2000 Hauser MA, Horrigan SK, Salmikangas P, Torian UM, Viles KD, Dancel R, Tim RW, Taivainen A, Bartoloni L, Gilchrist JM, Stajich JM, Gaskell PC, Gilbert JR, Vance JM, Pericak-Vance MA, et al. Myotilin is mutated in limb girdle muscular dystrophy 1A. Human Molecular Genetics. 9: 2141-7. PMID 10958653 DOI: 10.1093/Hmg/9.14.2141  0.16
2000 Wolpert CM, Menold MM, Bass MP, Qumsiyeh MB, Donnelly SL, Ravan SA, Vance JM, Gilbert JR, Abramson RK, Wright HH, Cuccaro ML, Pericak-Vance MA. Three probands with autistic disorder and isodicentric chromosome 15. American Journal of Medical Genetics. 96: 365-72. PMID 10898916 DOI: 10.1002/1096-8628(20000612)96:3<365::Aid-Ajmg25>3.0.Co;2-X  0.16
2000 Donnelly SL, Wolpert CM, Menold MM, Bass MP, Gilbert JR, Cuccaro ML, Delong GR, Pericak-Vance MA. Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome. American Journal of Medical Genetics. 96: 312-6. PMID 10898907 DOI: 10.1002/1096-8628(20000612)96:3<312::Aid-Ajmg16>3.0.Co;2-8  0.01
2000 Martin ER, Lai EH, Gilbert JR, Rogala AR, Afshari AJ, Riley J, Finch KL, Stevens JF, Livak KJ, Slotterbeck BD, Slifer SH, Warren LL, Conneally PM, Schmechel DE, Purvis I, et al. SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease. American Journal of Human Genetics. 67: 383-94. PMID 10869235 DOI: 10.1086/303003  0.16
2000 Martin ER, Menold MM, Wolpert CM, Bass MP, Donnelly SL, Ravan SA, Zimmerman A, Gilbert JR, Vance JM, Maddox LO, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA. Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder. American Journal of Medical Genetics. 96: 43-8. PMID 10686550 DOI: 10.1002/(Sici)1096-8628(20000207)96:1<43::Aid-Ajmg9>3.0.Co;2-3  0.16
2000 Gilbert JR, Kumar A, Newey S, Rao N, Ioannou P, Qiu H, Lin D, Xu P, Pettenati MJ, Pericak-Vance MA. Physical and cDNA mapping in the DBH region of human chromosome 9q34. Human Heredity. 50: 151-7. PMID 10686491 DOI: 10.1159/000022905  0.04
2000 Martin ER, Gilbert JR, Lai EH, Riley J, Rogala AR, Slotterbeck BD, Sipe CA, Grubber JM, Warren LL, Conneally PM, Saunders AM, Schmechel DE, Purvis I, Pericak-Vance MA, Roses AD, et al. Analysis of association at single nucleotide polymorphisms in the APOE region. Genomics. 63: 7-12. PMID 10662539 DOI: 10.1006/Geno.1999.6057  0.16
2000 Scott WK, Grubber JM, Conneally P, Small GW, Gilbert JR, Haines JL, Pericak-Vance MA. Fine-mapping of the chromosome 12 Alzheimer disease locus using family-based association tests of microsatellite markers Neurobiology of Aging. 21: 129. DOI: 10.1016/S0197-4580(00)82380-5  0
2000 Teter B, Gilbert JR, Roses AD, Xu P, Galasko D, Bu G, Cole GM. Human apolipoprotein E4 has a gain-of-negative-function in supporting mossy fiber axon sprouting in organotypic hippocampal slice culture Neurobiology of Aging. 21: 186. DOI: 10.1016/S0197-4580(00)82176-4  0
1999 Maddox LO, Menold MM, Bass MP, Rogala AR, Pericak-Vance MA, Vance JM, Gilbert JR. Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig. Genomics. 62: 325-31. PMID 10644429 DOI: 10.1006/Geno.1999.6017  0.01
1999 Teter B, Xu PT, Gilbert JR, Roses AD, Galasko D, Cole GM. Human apolipoprotein E isoform-specific differences in neuronal sprouting in organotypic hippocampal culture. Journal of Neurochemistry. 73: 2613-6. PMID 10582625 DOI: 10.1046/j.1471-4159.1999.0732613.x  0.16
1999 Ashley-Koch A, Wolpert CM, Menold MM, Zaeem L, Basu S, Donnelly SL, Ravan SA, Powell CM, Qumsiyeh MB, Aylsworth AS, Vance JM, Gilbert JR, Wright HH, Abramson RK, DeLong GR, et al. Genetic studies of autistic disorder and chromosome 7. Genomics. 61: 227-36. PMID 10552924 DOI: 10.1006/Geno.1999.5968  0.16
1999 Licastro F, Campbell IL, Kincaid C, Veinbergs I, Van Uden E, Rockenstein E, Mallory M, Gilbert JR, Masliah E. A role for apoE in regulating the levels of alpha-1-antichymotrypsin in the aging mouse brain and in Alzheimer's disease. The American Journal of Pathology. 155: 869-75. PMID 10487844 DOI: 10.1016/S0002-9440(10)65186-3  0.16
1999 De La Paz MA, Guy VK, Abou-Donia S, Heinis R, Bracken B, Vance JM, Gilbert JR, Gass JD, Haines JL, Pericak-Vance MA. Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration. Ophthalmology. 106: 1531-6. PMID 10442900 DOI: 10.1016/S0161-6420(99)90449-9  0.01
1999 Veinbergs I, Mallory M, Mante M, Rockenstein E, Gilbert JR, Masliah E. Differential neurotrophic effects of apolipoprotein E in aged transgenic mice. Neuroscience Letters. 265: 218-22. PMID 10327170 DOI: 10.1016/S0304-3940(99)00243-8  0.16
1999 Xu PT, Schmechel D, Qiu HL, Herbstreith M, Rothrock-Christian T, Eyster M, Roses AD, Gilbert JR. Sialylated human apolipoprotein E (apoEs) is preferentially associated with neuron-enriched cultures from APOE transgenic mice. Neurobiology of Disease. 6: 63-75. PMID 10078974 DOI: 10.1006/Nbdi.1998.0213  0.16
1999 Xu PT, Gilbert JR, Qiu HL, Ervin J, Rothrock-Christian TR, Hulette C, Schmechel DE. Specific regional transcription of apolipoprotein E in human brain neurons. The American Journal of Pathology. 154: 601-11. PMID 10027417 DOI: 10.1016/S0002-9440(10)65305-9  0.16
1998 Gilbert JR, Guy V, Kumar A, Wolpert C, Kandt R, Aylesworth A, Roses AD, Pericak-Vance MA. Mutation and polymorphism analysis in the tuberous sclerosis 2 (TSC2) gene. Neurogenetics. 1: 267-72. PMID 10732801 DOI: 10.1007/S100480050039  0.16
1998 Xu PT, Gilbert JR, Qiu HL, Rothrock-Christian T, Settles DL, Roses AD, Schmechel DE. Regionally specific neuronal expression of human APOE gene in transgenic mice. Neuroscience Letters. 246: 65-8. PMID 9627181 DOI: 10.1016/S0304-3940(98)00247-X  0.16
1997 Speer MC, Pericak-Vance MA, Stajich JM, Sarrica J, Jordan M, Roses AD, Vance JM, Gilbert JR. Further exclusion of FSHD1B from the telomeric region of 10q. Neurogenetics. 1: 151-2. PMID 10732819 DOI: 10.1007/S100480050023  0.16
1996 Xu PT, Schmechel D, Rothrock-Christian T, Burkhart DS, Qiu HL, Popko B, Sullivan P, Maeda N, Saunders AM, Roses AD, Gilbert JR. Human apolipoprotein E2, E3, and E4 isoform-specific transgenic mice: human-like pattern of glial and neuronal immunoreactivity in central nervous system not observed in wild-type mice. Neurobiology of Disease. 3: 229-45. PMID 8980023 DOI: 10.1006/Nbdi.1996.0023  0.16
1996 Speer MC, Tandan R, Rao PN, Fries T, Stajich JM, Bolhuis PA, Jöbsis GJ, Vance JM, Viles KD, Sheffield K, James C, Kahler SG, Pettenati M, Gilbert JR, Denton PH, et al. Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37. Human Molecular Genetics. 5: 1043-6. PMID 8817344 DOI: 10.1093/Hmg/5.7.1043  0.16
1996 Boteva K, Vitek M, Mitsuda H, de Silva H, Xu PT, Small G, Gilbert JR. Mutation analysis of presenillin 1 gene in Alzheimer's disease. Lancet. 347: 130-1. PMID 8538334 DOI: 10.1016/S0140-6736(96)90261-5  0.04
1996 Stopa E, Vitek M, Rubin B, Schmechel D, Kuo-Leblanc. V, Wei Y, Song P, King J, Boteva K, Mitsuda N, Gilbert J, Roses A. 67 In-situ localization of S182 mRNA in sporadic Alzheimer's disease (AD) Neurobiology of Aging. 17: S17. DOI: 10.1016/S0197-4580(96)80069-8  0
1995 Kumar A, Kandt RS, Wolpert C, Roses AD, Pericak-Vance MA, Gilbert JR. Mutation analysis of the TSC2 gene in an African-American family. Human Molecular Genetics. 4: 2295-8. PMID 8634701 DOI: 10.1093/Hmg/4.12.2295  0.01
1995 Gilbert JR, Speer MC, Stajich J, Clancy R, Lewis K, Qiu H, Yamaoka L, Kumar A, Vance J, Stewart C. Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B. Journal of Medical Genetics. 32: 770-3. PMID 8558552 DOI: 10.1136/Jmg.32.10.770  0.16
1995 Kumar A, Wolpert C, Kandt RS, Segal J, Pufky J, Roses AD, Pericak-Vance MA, Gilbert JR. A de novo frame-shift mutation in the tuberin gene. Human Molecular Genetics. 4: 1471-2. PMID 7581393 DOI: 10.1093/Hmg/4.8.1471  0.01
1994 Strittmatter WJ, Weisgraber KH, Goedert M, Saunders AM, Huang D, Corder EH, Dong LM, Jakes R, Alberts MJ, Gilbert JR. Hypothesis: microtubule instability and paired helical filament formation in the Alzheimer disease brain are related to apolipoprotein E genotype. Experimental Neurology. 125: 163-71; discussion 1. PMID 8313935 DOI: 10.1006/Exnr.1994.1019  0.16
1994 Samson F, Mesnard L, Mihovilovic M, Potter TG, Mercadier JJ, Roses AD, Gilbert JR. A new human slow skeletal troponin T (TnTs) mRNA isoform derived from alternative splicing of a single gene. Biochemical and Biophysical Research Communications. 199: 841-7. PMID 8135831 DOI: 10.1006/bbrc.1994.1305  0.16
1992 Samson F, de Jong PJ, Trask BJ, Koza-Taylor P, Speer MC, Potter T, Roses AD, Gilbert JR. Assignment of the human slow skeletal troponin T gene to 19q13.4 using somatic cell hybrids and fluorescence in situ hybridization analysis. Genomics. 13: 1374-5. PMID 1505979 DOI: 10.1016/0888-7543(92)90077-6  0.16
1991 Samson F, Gilbert JR, Koza-Taylor P, Speer MC, Lee J, Roses AD. A PstI polymorphism detected by a genomic clone at the human slow troponin T (TNNT1) gene locus. Nucleic Acids Research. 19: 6058. PMID 1682896 DOI: 10.1093/Nar/19.21.6058  0.16
1990 Samson F, Lee JE, Hung WY, Potter TG, Herbstreith M, Roses AD, Gilbert JR. Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNA. Journal of Neuroscience Research. 27: 441-51. PMID 1706783 DOI: 10.1002/jnr.490270403  0.01
1988 Schmechel DE, Goldgaber D, Burkhart DS, Gilbert JR, Gajdusek DC, Roses AD. Cellular localization of messenger RNA encoding amyloid-beta-protein in normal tissue and in Alzheimer disease. Alzheimer Disease and Associated Disorders. 2: 96-111. PMID 3063300 DOI: 10.1097/00002093-198802020-00002  0.16
1987 Bartlett RJ, Pericak-Vance MA, Lanman JT, Killam AP, Gilbert JR, Stajick JM, Chen JC, Siddique T, Kandt RS, Sirotkin-Roses M. Prenatal detection of an inherited Duchenne muscular dystrophy deletion allele. Neurology. 37: 355-6. PMID 3808324 DOI: 10.1212/Wnl.37.2.355  0.04
1987 Koh J, Bartlett RJ, Pericak-Vance MA, Speer MC, Yamaoka LH, Phillips K, Hung WY, Ray PN, Worton RG, Gilbert JR. Inherited deletion at Duchenne dystrophy locus in normal male. Lancet. 2: 1154-5. PMID 2890056 DOI: 10.1016/S0140-6736(87)91590-X  0.16
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