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Results: 1 to 20 of 181

1.

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.

J Med Genet. 2005 Dec;42(12):940-6. Epub 2005 Apr 14.

PMID:
15831595
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Refinement of 2q and 7p loci in a large multiplex NTD family.

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; NTD Collaborative Group.

Birth Defects Res A Clin Mol Teratol. 2008 Jun;82(6):441-52. doi: 10.1002/bdra.20462.

PMID:
18452155
[PubMed - indexed for MEDLINE]
3.

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.

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; NTD Collaborative Group.

Birth Defects Res A Clin Mol Teratol. 2006 Jun;76(6):499-505.

PMID:
16933213
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X.

Stine OC, McMahon FJ, Chen L, Xu J, Meyers DA, MacKinnon DF, Simpson S, McInnis MG, Rice JP, Goate A, Reich T, Edenberg HJ, Foroud T, Nurnberger JI Jr, Detera-Wadleigh SD, Goldin LR, Guroff J, Gershon ES, Blehar MC, DePaulo JR.

Am J Med Genet. 1997 May 31;74(3):263-9.

PMID:
9184308
[PubMed - indexed for MEDLINE]
5.

Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects.

Volcik KA, Blanton SH, Kruzel MC, Townsend IT, Tyerman GH, Mier RJ, Northrup H.

Am J Med Genet. 2002 Jul 1;110(3):203-7.

PMID:
12116226
[PubMed - indexed for MEDLINE]
6.

Absence of linkage between familial neural tube defects and PAX3 gene.

Chatkupt S, Hol FA, Shugart YY, Geurds MP, Stenroos ES, Koenigsberger MR, Hamel BC, Johnson WG, Mariman EC.

J Med Genet. 1995 Mar;32(3):200-4.

PMID:
7783169
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Methionine synthase: high-resolution mapping of the human gene and evaluation as a candidate locus for neural tube defects.

Brody LC, Baker PJ, Chines PS, Musick A, Molloy AM, Swanson DA, Kirke PN, Ghosh S, Scott JM, Mills JL.

Mol Genet Metab. 1999 Aug;67(4):324-33.

PMID:
10444343
[PubMed - indexed for MEDLINE]
8.

Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12.

Rice JP, Goate A, Williams JT, Bierut L, Dorr D, Wu W, Shears S, Gopalakrishnan G, Edenberg HJ, Foroud T, Nurnberger J Jr, Gershon ES, Detera-Wadleigh SD, Goldin LR, Guroff JJ, McMahon FJ, Simpson S, MacKinnon D, McInnis M, Stine OC, DePaulo JR, Blehar MC, Reich T.

Am J Med Genet. 1997 May 31;74(3):247-53.

PMID:
9184306
[PubMed - indexed for MEDLINE]
9.

Modifier locus for exencephaly in Cecr2 mutant mice is syntenic to the 10q25.3 region associated with neural tube defects in humans.

Davidson CE, Li Q, Churchill GA, Osborne LR, McDermid HE.

Physiol Genomics. 2007 Oct 22;31(2):244-51. Epub 2007 Jul 10.

PMID:
17623803
[PubMed - indexed for MEDLINE]
Free Article
10.

[Epidemiological study on reduced folate carrier gene(RFC1 A80G) polymorphism and other risk factors of neural tube defects].

Pei LJ, Li ZW, Zhang W, Ren AG, Zhu HP, Hao L, Zhu JH, Li Z.

Beijing Da Xue Xue Bao. 2005 Aug 18;37(4):341-5. Chinese.

PMID:
16086047
[PubMed - indexed for MEDLINE]
Free Article
11.

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.

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, Mueller D, Oro' JJ, Iskandar BJ, George TM, Milhorat TH, Speer MC.

Am J Med Genet A. 2006 Dec 15;140(24):2776-85.

PMID:
17103432
[PubMed - indexed for MEDLINE]
12.

A full genome scan for age-related maculopathy.

Weeks DE, Conley YP, Mah TS, Paul TO, Morse L, Ngo-Chang J, Dailey JP, Ferrell RE, Gorin MB.

Hum Mol Genet. 2000 May 22;9(9):1329-49.

PMID:
10814715
[PubMed - indexed for MEDLINE]
Free Article
13.

Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.

Mineharu Y, Inoue K, Inoue S, Yamada S, Nozaki K, Hashimoto N, Koizumi A.

Stroke. 2007 Apr;38(4):1174-8. Epub 2007 Feb 22.

PMID:
17322081
[PubMed - indexed for MEDLINE]
Free Article
14.

A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.

Hauser ER, Crossman DC, Granger CB, Haines JL, Jones CJ, Mooser V, McAdam B, Winkelmann BR, Wiseman AH, Muhlestein JB, Bartel AG, Dennis CA, Dowdy E, Estabrooks S, Eggleston K, Francis S, Roche K, Clevenger PW, Huang L, Pedersen B, Shah S, Schmidt S, Haynes C, West S, Asper D, Booze M, Sharma S, Sundseth S, Middleton L, Roses AD, Hauser MA, Vance JM, Pericak-Vance MA, Kraus WE.

Am J Hum Genet. 2004 Sep;75(3):436-47. Epub 2004 Jul 22.

PMID:
15272420
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.

Wilson SG, Adam G, Langdown M, Reneland R, Braun A, Andrew T, Surdulescu GL, Norberg M, Dudbridge F, Reed PW, Sambrook PN, Kleyn PW, Spector TD.

Eur J Hum Genet. 2006 Mar;14(3):340-8.

PMID:
16391564
[PubMed - indexed for MEDLINE]
Free Article
16.

Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study.

Sutton BS, Langefeld CD, Campbell JK, Haffner SM, Norris JM, Scherzinger AL, Wagenknecht LE, Bowden DW.

Int J Obes (Lond). 2006 Sep;30(9):1433-41. Epub 2006 Mar 7.

PMID:
16520807
[PubMed - indexed for MEDLINE]
17.

Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.

Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, Medrano M, Arriaga A, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R.

Arch Neurol. 2006 Nov;63(11):1591-8.

PMID:
17101828
[PubMed - indexed for MEDLINE]
18.

Two-stage genome-wide linkage scan in keratoconus sib pair families.

Li X, Rabinowitz YS, Tang YG, Picornell Y, Taylor KD, Hu M, Yang H.

Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3791-5.

PMID:
16936089
[PubMed - indexed for MEDLINE]
Free Article
19.

Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree.

Panhuysen CI, Karban A, Knodle Manning A, Bayless TM, Duerr RH, Bailey-Wilson JE, Epstein EH Jr, Brant SR.

Hum Genet. 2006 Aug;120(1):31-41. Epub 2006 May 30.

PMID:
16733713
[PubMed - indexed for MEDLINE]
20.

Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.

Chapman NH, Igo RP, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Berninger VW, Wijsman EM, Raskind WH.

Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):67-75.

PMID:
15389770
[PubMed - indexed for MEDLINE]
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