Genomic analyses : A neonatology perspectiveGOTTEN, C. Michael; GINSBURG, Geoffrey S; GOLDBERG, Ronald N et al.The Journal of pediatrics. 2006, Vol 148, Num 6, pp 720-726, issn 0022-3476, 7 p.Article

Candidate gene analysis in human neural tube defectsBOYLES, Abee L; HAMMOCK, Preston; SPEER, Marcy C et al.American journal of medical genetics. 2005, Vol 135C, Num 1, pp 9-23, issn 0148-7299, 15 p.Conference Paper

Genetic Association Analyses of Nitric Oxide Synthase Genes and Neural Tube Defects Vary by PhenotypeSOLDANO, Karen L; GARRETT, Melanie E; COPE, Heidi L et al.Birth defects research. Part B. Developmental and reproductive toxicology. 2013, Vol 98, Num 5, pp 364-372, issn 1542-9733, 9 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

Clinical and pathologic features of familial interstitial pneumoniaSTEELE, Mark P; SPEER, Marcy C; MCADAMS, H. Page et al.American journal of respiratory and critical care medicine. 2005, Vol 172, Num 9, pp 1146-1152, issn 1073-449X, 7 p.Article

Human neural tube defects : Developmental biology, epidemiology, and geneticsDETRAIT, Eric R; GEORGE, Timothy M; ETCHEVERS, Heather C et al.Neurotoxicology and teratology. 2005, Vol 27, Num 3, pp 515-524, issn 0892-0362, 10 p.Article

Folate metabolism genes, dietary folate and response to antidepressant medications in late-life depressionJAMERSON, Brenda D; PAYNE, Martha E; GARRETT, Melanie E et al.International journal of geriatric psychiatry. 2013, Vol 28, Num 9, pp 925-932, issn 0885-6230, 8 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

T Locus shows no evidence for linkage disequilibrium or mutation in American caucasian neural tube defect familiesSPEER, Marcy C; MELVIN, Elizabeth C; GILBERT, John R et al.American journal of medical genetics. 2002, Vol 110, Num 3, pp 215-218, issn 0148-7299Article

Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432SPEER, Marcy C; GRAHAM, Felicia Lennon; BONNER, Erin et al.Neurogenetics (Oxford. Print). 2002, Vol 4, Num 2, pp 83-85, issn 1364-6745, 3 p.Article

Familial pulmonary fibrosis in the United StatesWAHIDI, Momen M; SPEER, Marcy C; STEELE, Mark P et al.Chest. 2002, Vol 121, Num 3, issn 0012-3692, p. 30S, SUPConference Paper

Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations: Clinical articleMARKUNAS, Christina A; SHANE TUBBS, R; MOFTAKHAR, Roham et al.Journal of neurosurgery. Pediatrics. 2012, Vol 9, Num 4, pp 372-378, issn 1933-0707, 7 p.Article

Native American Myopathy : Congenital Myopathy With Cleft Palate, Skeletal Anomalies, and Susceptibility to Malignant HyperthermiaSTAMM, Demetra S; AYLSWORTH, Arthur S; STAJICH, Jeffrey M et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 14, pp 1832-1841, issn 1552-4825, 10 p.Article

Estimated Fumonisin Exposure in Guatemala Is Greatest in Consumers of Lowland MaizeTORRES, Olga A; PALENCIA, Edwin; RILEY, Ronald T et al.The Journal of nutrition. 2007, Vol 137, Num 12, pp 2723-2729, issn 0022-3166, 7 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

A Common MUC5B Promoter Polymorphism and Pulmonary FibrosisSEIBOLD, Max A; WISE, Anastasia L; EVANS, Christopher M et al.The New England journal of medicine. 2011, Vol 364, Num 16, pp 1503-1512, issn 0028-4793, 10 p.Article

Human neural crest cells display molecular and phenotypic hallmarks of stem cellsTHOMAS, Sophie; THOMAS, Marie; WINCKER, Patrick et al.Human molecular genetics (Print). 2008, Vol 17, Num 21, pp 3411-3425, issn 0964-6906, 15 p.Article

Gene expression profiling of familial and sporadic interstitial pneumoniaYANG, Ivana V; BURCH, Lauranell H; SCHWARZ, Marvin I et al.American journal of respiratory and critical care medicine. 2007, Vol 175, Num 1, pp 45-54, issn 1073-449X, 10 p.Article

SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defectsDEAK, Kristen L; BOYLES, Abee L; MCCLAY, David et al.Human genetics. 2005, Vol 117, Num 2-3, pp 133-142, issn 0340-6717, 10 p.Article

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth diseaseZÜCHNER, Stephan; NOUREDDINE, Maher; WALIZADA, Gina et al.Nature genetics. 2005, Vol 37, Num 3, pp 289-294, issn 1061-4036, 6 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

Myotilin Mutation found in second pedigree with LGMD1AHAUSER, Michael A; CONDE, Cecilia B; KOWALJOW, Valeria et al.American journal of human genetics. 2002, Vol 71, Num 6, pp 1428-1432, issn 0002-9297, 5 p.Article

Investigation of Notch3 as a candidate gene for bipolar disorder using brain hyperintensities as an endophenotypeAHEARN, Eileen P; SPEER, Marcy C; CHEN, Y. T et al.American journal of medical genetics. 2002, Vol 114, Num 6, pp 652-658, issn 0148-7299Article