Leach RJ - Search Results

1

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication.

Timmerman V, Nelis E, Van Hul W, Nieuwenhuijsen BW, Chen KL, Wang S, Ben Othman K, Cullen B, Leach RJ, Hanemann CO, et al. Timmerman V, et al. Among authors: leach rj. Nat Genet. 1992 Jun;1(3):171-5. doi: 10.1038/ng0692-171. Nat Genet. 1992. PMID: 1303230

2

Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.

Wang A, Shen J, Rodriguez AA, Saunders EJ, Chen F, Janivara R, Darst BF, Sheng X, Xu Y, Chou AJ, Benlloch S, Dadaev T, Brook MN, Plym A, Sahimi A, Hoffman TJ, Takahashi A, Matsuda K, Momozawa Y, Fujita M, Laisk T, Figuerêdo J, Muir K, Ito S, Liu X; Biobank Japan Project; Uchio Y, Kubo M, Kamatani Y, Lophatananon A, Wan P, Andrews C, Lori A, Choudhury PP, Schleutker J, Tammela TLJ, Sipeky C, Auvinen A, Giles GG, Southey MC, MacInnis RJ, Cybulski C, Wokolorczyk D, Lubinski J, Rentsch CT, Cho K, Mcmahon BH, Neal DE, Donovan JL, Hamdy FC, Martin RM, Nordestgaard BG, Nielsen SF, Weischer M, Bojesen SE, Røder A, Stroomberg HV, Batra J, Chambers S, Horvath L, Clements JA, Tilly W, Risbridger GP, Gronberg H, Aly M, Szulkin R, Eklund M, Nordstrom T, Pashayan N, Dunning AM, Ghoussaini M, Travis RC, Key TJ, Riboli E, Park JY, Sellers TA, Lin HY, Albanes D, Weinstein S, Cook MB, Mucci LA, Giovannucci E, Lindstrom S, Kraft P, Hunter DJ, Penney KL, Turman C, Tangen CM, Goodman PJ, Thompson IM Jr, Hamilton RJ, Fleshner NE, Finelli A, Parent MÉ, Stanford JL, Ostrander EA, Koutros S, Beane Freeman LE, Stampfer M, Wolk A, Håkansson N, Andriole GL, Hoover RN, Machiela MJ, Sørensen KD, Borre M, Blot … See abstract for full author list ➔ Wang A, et al. Among authors: leach rj. Nat Genet. 2023 Dec;55(12):2065-2074. doi: 10.1038/s41588-023-01534-4. Epub 2023 Nov 9. Nat Genet. 2023. PMID: 37945903 Free PMC article.

3

Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p.

Whitney M, Thayer M, Reifsteck C, Olson S, Smith L, Jakobs PM, Leach R, Naylor S, Joenje H, Grompe M. Whitney M, et al. Nat Genet. 1995 Nov;11(3):341-3. doi: 10.1038/ng1195-341. Nat Genet. 1995. PMID: 7581463

4

Growth hormone insufficiency associated with haploinsufficiency at 18q23.

Cody JD, Hale DE, Brkanac Z, Kaye CI, Leach RJ. Cody JD, et al. Among authors: leach rj. Am J Med Genet. 1997 Sep 5;71(4):420-5. Am J Med Genet. 1997. PMID: 9286448

5

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.

Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, Ronen GM, Bjerre I, Quattlebaum T, Murphy JV, McHarg ML, Gagnon D, Rosales TO, Peiffer A, Anderson VE, Leppert M. Singh NA, et al. Among authors: leach rj. Nat Genet. 1998 Jan;18(1):25-9. doi: 10.1038/ng0198-25. Nat Genet. 1998. PMID: 9425895

6

Linkage of high-density lipoprotein-cholesterol concentrations to a locus on chromosome 9p in Mexican Americans.

Arya R, Duggirala R, Almasy L, Rainwater DL, Mahaney MC, Cole S, Dyer TD, Williams K, Leach RJ, Hixson JE, MacCluer JW, O'Connell P, Stern MP, Blangero J. Arya R, et al. Among authors: leach rj. Nat Genet. 2002 Jan;30(1):102-5. doi: 10.1038/ng810. Epub 2001 Dec 17. Nat Genet. 2002. PMID: 11743583

7

Linkage disequilibrium analyses in the Costa Rican population suggests discrete gene loci for schizophrenia at 8p23.1 and 8q13.3.

Walss-Bass C, Montero AP, Armas R, Dassori A, Contreras SA, Liu W, Medina R, Levinson D, Pereira M, Atmella I, NeSmith L, Leach R, Almasy L, Raventos H, Escamilla MA. Walss-Bass C, et al. Psychiatr Genet. 2006 Aug;16(4):159-68. doi: 10.1097/01.ypg.0000218616.27515.67. Psychiatr Genet. 2006. PMID: 16829783

8

Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiency.

Gay CT, Hardies LJ, Rauch RA, Lancaster JL, Plaetke R, DuPont BR, Cody JD, Cornell JE, Herndon RC, Ghidoni PD, Schiff JM, Kaye CI, Leach RJ, Fox PT. Gay CT, et al. Among authors: leach rj. Am J Med Genet. 1997 Jul 25;74(4):422-31. doi: 10.1002/(sici)1096-8628(19970725)74:4<422::aid-ajmg14>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9259379

9

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.

Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, Leppert M. Charlier C, et al. Among authors: leach rj. Nat Genet. 1998 Jan;18(1):53-5. doi: 10.1038/ng0198-53. Nat Genet. 1998. PMID: 9425900

10

Evidence for a novel osteosarcoma tumor-suppressor gene in the chromosome 18 region genetically linked with Paget disease of bone.

Nellissery MJ, Padalecki SS, Brkanac Z, Singer FR, Roodman GD, Unni KK, Leach RJ, Hansen MF. Nellissery MJ, et al. Among authors: leach rj. Am J Hum Genet. 1998 Sep;63(3):817-24. doi: 10.1086/302019. Am J Hum Genet. 1998. PMID: 9718349 Free PMC article.

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