A note on the column elimination treeGILBERT, John R; GRIGORI, Laura.SIAM journal on matrix analysis and applications. 2003, Vol 25, Num 1, pp 143-151, issn 0895-4798, 9 p.Article

SYMBOLIC AND EXACT STRUCTURE PREDICTION FOR SPARSE GAUSSIAN ELIMINATION WITH PARTIAL PIVOTINGGRIGORI, Laura; GILBERT, John R; COSNARD, Michel et al.SIAM journal on matrix analysis and applications. 2009, Vol 30, Num 4, pp 1520-1545, issn 0895-4798, 26 p.Article

Exploring the Relationship Between Autism Spectrum Disorder and Epilepsy Using Latent Class Cluster AnalysisCUCCARO, Michael L; TUCHMAN, Roberto F; HAMILTON, Kara L et al.Journal of autism and developmental disorders. 2012, Vol 42, Num 8, pp 1630-1641, issn 0162-3257, 12 p.Article

Microduplications in an Autism Multiplex Family Narrow the Region of Susceptibility for Developmental Disorders on 15q24 and Implicate 7p21CUKIER, Holly N; SALYAKINA, Daria; HAINES, Jonathan L et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2011, Vol 156, Num 4, pp 493-501, issn 1552-4841, 9 p.Article

Genome-wide Association Study Implicates a Chromosome 12 Risk Locus for Late-Onset Alzheimer DiseaseBEECHAM, Gary W; MARTIN, Eden R; LI, Yi-Ju et al.American journal of human genetics. 2009, Vol 84, Num 1, pp 35-43, issn 0002-9297, 9 p.Article

TERC is not a major gene in human neural tube defectsBENZ, Lisa P; SWIFT, Frances E; GEORGE, Timothy M et al.Birth defects research. Clinical and molecular teratology. 2004, Vol 70, Num 8, pp 531-533, issn 1542-0752, 3 p.Article

Resolving the relationship between ApolipoproteinE and depressionSLIFER, Michael A; MARTIN, Eden R; GILBERT, John R et al.Neuroscience letters. 2009, Vol 455, Num 2, pp 116-119, issn 0304-3940, 4 p.Article

Association analysis of genetic polymorphisms in the CDC2 gene with late-onset Alzheimer diseaseXUEYING LIANG; SCHNETZ-BOUTAUD, Nathalie; BARTLETT, Jackie et al.Dementia and geriatric cognitive disorders. 2007, Vol 23, Num 2, pp 126-132, issn 1420-8008, 7 p.Article

Functional candidate genes in age-related macular degeneration : Significant association with VEGF, VLDLR, and LRP6HAINES, Jonathan L; SCHNETZ-BOUTAUD, Nathalie; PERICAK-VANCE, Margaret A et al.Investigative ophthalmology & visual science. 2006, Vol 47, Num 1, pp 329-335, issn 0146-0404, 7 p.Article

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 15BOYLES, Abee L; ENTERLINE, David S; BENZEL, Edward et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 24, pp 2776-2785, issn 1552-4825, 10 p.Article

Complement factor H variant increases the risk of age-related macular degenerationHAINES, Jonathan L; HAUSER, Michael A; SCHNETZ-BOUTAUD, Nathalie et al.Science (Washington, D.C.). 2005, Vol 308, Num 5720, pp 419-421, issn 0036-8075, 3 p.Article

Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West AfricansVELEZ, Digna Rosa; WEJSE, Christian; SIRUGO, Giorgio et al.Human genetics. 2010, Vol 127, Num 1, pp 65-73, issn 0340-6717, 9 p.Article

Factor analysis of the aberrant behavior checklist in individuals with autism spectrum disordersBRINKLEY, Jason; NATIONS, Laura; ABRAMSON, Ruth K et al.Journal of autism and developmental disorders. 2007, Vol 37, Num 10, pp 1949-1959, issn 0162-3257, 11 p.Article

Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2DEAK, Kristen L; DICKERSON, Margaret E; BASSUK, Alexander G et al.Birth defects research. Clinical and molecular teratology. 2005, Vol 73, Num 11, pp 868-875, issn 1542-0752, 8 p.Article

Detailed analysis of allelic variation in the ABCA4 gene in age-related maculopathySCHMIDT, Silke; POSTEL, Eric A; AGARWAL, Anita et al.Investigative ophthalmology & visual science. 2003, Vol 44, Num 7, pp 2868-2875, issn 0146-0404, 8 p.Article

Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson diseaseLI, Yi-Ju; OLIVEIRA, Sofia A; WATTS, Ray L et al.Human molecular genetics (Print). 2003, Vol 12, Num 24, pp 3259-3267, issn 0964-6906, 9 p.Article

Genomic screen and follow-up analysis for autistic disorderYUJUN SHAO; WOLPERT, Chantelle M; ABRAMSON, Ruth H et al.American journal of medical genetics. 2002, Vol 114, Num 1, pp 99-105, issn 0148-7299Article

Novel variants identified in methyl-CpG-binding domain genes in autistic individualsCUKIER, Holly N; RABIONET, Raquel; GILBERT, John R et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 3, pp 291-303, issn 1364-6745, 13 p.Article

Autism in African American Families : Clinical-Phenotypic FindingsCUCCARO, Michael L; BRINKLEY, Jason; ABRAMSON, Ruth K et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2007, Vol 144, Num 8, pp 1022-1026, issn 1552-4841, 5 p.Article

Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysisLIN, Ping-I; MARTIN, Eden R; BROWNING-LARGE, Carrie A et al.Neurogenetics (Oxford. Print). 2006, Vol 7, Num 3, pp 157-165, issn 1364-6745, 9 p.Article

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-q35STAMM, Demetra S; RAMPERSAUD, Evadnie; GILBERT, John R et al.Birth defects research. Clinical and molecular teratology. 2006, Vol 76, Num 6, pp 499-505, issn 1542-0752, 7 p.Conference Paper

Lack of association between autism and SLC25A12RABIONET, Raquel; MCCAULEY, Jacob L; CUCCARO, Michael L et al.The American journal of psychiatry. 2006, Vol 163, Num 5, pp 929-931, issn 0002-953X, 3 p.Article

Analysis of European mitochondrial haplogroups with Alzheimer disease riskVAN DER WALT, Joelle M; DEMENTIEVA, Yulia A; SCHMECHEL, Donald E et al.Neuroscience letters. 2004, Vol 365, Num 1, pp 28-32, issn 0304-3940, 5 p.Article

Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genesRABIONET, Raquel; JAWORSKI, James M; GILBERT, John R et al.Neuroscience letters. 2004, Vol 372, Num 3, pp 209-214, issn 0304-3940, 6 p.Article

No association between the WNT2 gene and autistic disorderMCCOY, Pinky A; YUJUN SHAO; CUCCARO, Michael L et al.American journal of medical genetics. 2002, Vol 114, Num 1, pp 106-109, issn 0148-7299Article