Barrett T - Search Results

1

The relationship between Y chromosome DNA haplotypes and Y chromosome deletions leading to male infertility.

Quintana-Murci L, Krausz C, Heyer E, Gromoll J, Seifer I, Barton DE, Barrett T, Skakkebaek NE, Rajpert-De Meyts E, Mitchell M, Lee AC, Jobling MA, McElreavey K. Quintana-Murci L, et al. Among authors: barrett t. Hum Genet. 2001 Jan;108(1):55-8. doi: 10.1007/s004390000424. Hum Genet. 2001. PMID: 11214908

2

Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility.

Rovio AT, Marchington DR, Donat S, Schuppe HC, Abel J, Fritsche E, Elliott DJ, Laippala P, Ahola AL, McNay D, Harrison RF, Hughes B, Barrett T, Bailey DM, Mehmet D, Jequier AM, Hargreave TB, Kao SH, Cummins JM, Barton DE, Cooke HJ, Wei YH, Wichmann L, Poulton J, Jacobs HT. Rovio AT, et al. Among authors: barrett t. Nat Genet. 2001 Nov;29(3):261-2. doi: 10.1038/ng759. Nat Genet. 2001. PMID: 11687794

3

Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping.

Neufeld EJ, Mandel H, Raz T, Szargel R, Yandava CN, Stagg A, Fauré S, Barrett T, Buist N, Cohen N. Neufeld EJ, et al. Among authors: barrett t. Am J Hum Genet. 1997 Dec;61(6):1335-41. doi: 10.1086/301642. Am J Hum Genet. 1997. PMID: 9399900 Free PMC article.

4

Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneity.

Raz T, Barrett T, Szargel R, Mandel H, Neufeld EJ, Nosaka K, Viana MB, Cohen N. Raz T, et al. Among authors: barrett t. Hum Genet. 1998 Oct;103(4):455-61. doi: 10.1007/s004390050850. Hum Genet. 1998. PMID: 9856490

5

EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome.

Delépine M, Nicolino M, Barrett T, Golamaully M, Lathrop GM, Julier C. Delépine M, et al. Among authors: barrett t. Nat Genet. 2000 Aug;25(4):406-9. doi: 10.1038/78085. Nat Genet. 2000. PMID: 10932183

6

Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity.

Senée V, Vattem KM, Delépine M, Rainbow LA, Haton C, Lecoq A, Shaw NJ, Robert JJ, Rooman R, Diatloff-Zito C, Michaud JL, Bin-Abbas B, Taha D, Zabel B, Franceschini P, Topaloglu AK, Lathrop GM, Barrett TG, Nicolino M, Wek RC, Julier C. Senée V, et al. Diabetes. 2004 Jul;53(7):1876-83. doi: 10.2337/diabetes.53.7.1876. Diabetes. 2004. PMID: 15220213

7

Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness.

Labay V, Raz T, Baron D, Mandel H, Williams H, Barrett T, Szargel R, McDonald L, Shalata A, Nosaka K, Gregory S, Cohen N. Labay V, et al. Among authors: barrett t. Nat Genet. 1999 Jul;22(3):300-4. doi: 10.1038/10372. Nat Genet. 1999. PMID: 10391221

8

Genetic predictors of cardiovascular morbidity in Bardet-Biedl syndrome.

Forsythe E, Sparks K, Hoskins BE, Bagkeris E, McGowan BM, Carroll PV, Huda MS, Mujahid S, Peters C, Barrett T, Mohammed S, Beales PL. Forsythe E, et al. Among authors: barrett t. Clin Genet. 2015 Apr;87(4):343-9. doi: 10.1111/cge.12373. Epub 2014 Apr 8. Clin Genet. 2015. PMID: 24611735 Free PMC article.

9

The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight families.

Raz T, Labay V, Baron D, Szargel R, Anbinder Y, Barrett T, Rabl W, Viana MB, Mandel H, Baruchel A, Cayuela JM, Cohen N. Raz T, et al. Among authors: barrett t. Hum Mutat. 2000;16(1):37-42. doi: 10.1002/1098-1004(200007)16:1<37::AID-HUMU7>3.0.CO;2-9. Hum Mutat. 2000. PMID: 10874303

10

Prader-Willi Syndrome: guidance for children and transition into adulthood.

Shaikh MG, Barrett T, Bridges N, Chung R, Gevers E, Goldstone AP, Holland A, Kanumakala S, Krone RE, Kyriakou A, Livesey EA, Lucas-Herald A, Meade C, Passmore S, Roche E, Smith C, Soni S. Shaikh MG, et al. Among authors: barrett t. Endocr Connect. 2024 Jun 1:EC-24-0091. doi: 10.1530/EC-24-0091. Online ahead of print. Endocr Connect. 2024. PMID: 38838713 Review.

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