Nye J - Search Results

1

Genetic studies in neural tube defects. NTD Collaborative Group.

Melvin EC, George TM, Worley G, Franklin A, Mackey J, Viles K, Shah N, Drake CR, Enterline DS, McLone D, Nye J, Oakes WJ, McLaughlin C, Walker ML, Peterson P, Brei T, Buran C, Aben J, Ohm B, Bermans I, Qumsiyeh M, Vance J, Pericak-Vance MA, Speer MC. Melvin EC, et al. Among authors: nye j. Pediatr Neurosurg. 2000 Jan;32(1):1-9. doi: 10.1159/000028889. Pediatr Neurosurg. 2000. PMID: 10765131 Review.

2

Recurrence risks for neural tube defects in siblings of patients with lipomyelomeningocele.

Sebold CD, Melvin EC, Siegel D, Mehltretter L, Enterline DS, Nye JS, Kessler J, Bassuk A, Speer MC, George TM; NTD Collaborative Group. Sebold CD, et al. Among authors: nye js. Genet Med. 2005 Jan;7(1):64-7. doi: 10.1097/01.gim.0000151158.09278.2b. Genet Med. 2005. PMID: 15654231

3

T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families.

Speer MC, Melvin EC, Viles KD, Bauer KA, Rampersaud E, Drake C, George TM, Enterline DS, Mackey JF, Worley G, Gilbert JR, Nye JS; NTD Collaborative Group. Neural Tube Defects. Speer MC, et al. Am J Med Genet. 2002 Jul 1;110(3):215-8. doi: 10.1002/ajmg.10436. Am J Med Genet. 2002. PMID: 12116228

4

A novel mutation in the gene encoding noggin is not causative in human neural tube defects.

Bauer KA, George TM, Enterline DS, Stottmann RW, Melvin EC, Siegel D, Samal S, Hauser MA, Klingensmith J, Nye JS, Speer MC; Neural Tube Defects Collaborative Group. Bauer KA, et al. Among authors: nye js. J Neurogenet. 2002 Jan-Mar;16(1):65-71. J Neurogenet. 2002. PMID: 12420790

5

Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative Group.

Speer MC, Nye J, McLone D, Worley G, Melvin EC, Viles KD, Franklin A, Drake C, Mackey J, George TM. Speer MC, et al. Among authors: nye j. Clin Genet. 1999 Aug;56(2):142-4. doi: 10.1034/j.1399-0004.1999.560208.x. Clin Genet. 1999. PMID: 10517251

6

Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10.

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, Ito J, Kessler JA, Lasarsky N, Mack P, Mackey J, McLone D, Meeropol E, Mehltretter L, Mitchell LE, Oakes WJ, Nye JS, Powell C, Sawin K, Stevenson R, Walker M, West SG, Worley G, Gilbert JR, Speer MC. Rampersaud E, et al. Among authors: nye js. J Med Genet. 2005 Dec;42(12):940-6. doi: 10.1136/jmg.2005.031658. Epub 2005 Apr 14. J Med Genet. 2005. PMID: 15831595 Free PMC article.

7

Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects.

Rampersaud E, Melvin EC, Siegel D, Mehltretter L, Dickerson ME, George TM, Enterline D, Nye JS, Speer MC; NTD Collaborative Group. Rampersaud E, et al. Among authors: nye js. Clin Genet. 2003 Mar;63(3):210-4. doi: 10.1034/j.1399-0004.2003.00043.x. Clin Genet. 2003. PMID: 12694231

8

Neural crest anomaly syndromes in children with spina bifida.

Nye JS, McLone DG, Charrow J, Hayes EA. Nye JS, et al. Teratology. 1999 Oct;60(4):179-89. doi: 10.1002/(SICI)1096-9926(199910)60:4<179::AID-TERA2>3.0.CO;2-U. Teratology. 1999. PMID: 10508971

9

Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: possible digenic inheritance of a neural tube defect.

Nye JS, Balkin N, Lucas H, Knepper PA, McLone DG, Charrow J. Nye JS, et al. Am J Med Genet. 1998 Feb 3;75(4):401-8. Am J Med Genet. 1998. PMID: 9482647

10

Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomalies.

Nye JS, Hayes EA, Amendola M, Vaughn D, Charrow J, McLone DG, Speer MC, Nance WE, Pandya A. Nye JS, et al. Teratology. 2000 Mar;61(3):165-71. doi: 10.1002/(SICI)1096-9926(200003)61:3<165::AID-TERA3>3.0.CO;2-E. Teratology. 2000. PMID: 10661905

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