Weiss B - Search Results

1

A human pseudoautosomal gene, ADP/ATP translocase, escapes X-inactivation whereas a homologue on Xq is subject to X-inactivation.

Schiebel K, Weiss B, Wöhrle D, Rappold G. Schiebel K, et al. Among authors: weiss b. Nat Genet. 1993 Jan;3(1):82-7. doi: 10.1038/ng0193-82. Nat Genet. 1993. PMID: 8490661

2

DXYS161 detects a VNTR locus in the pseudoautosomal region.

Weiss B, Rappold G. Weiss B, et al. Hum Mol Genet. 1994 Nov;3(11):2084. Hum Mol Genet. 1994. PMID: 7874142 No abstract available.

3

Double crossover in the human Xp/Yp pseudoautosomal region and its bearing on interference.

Rappold GA, Klink A, Weiss B, Fischer C. Rappold GA, et al. Among authors: weiss b. Hum Mol Genet. 1994 Aug;3(8):1337-40. doi: 10.1093/hmg/3.8.1337. Hum Mol Genet. 1994. PMID: 7987311

4

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome.

Rao E, Weiss B, Fukami M, Rump A, Niesler B, Mertz A, Muroya K, Binder G, Kirsch S, Winkelmann M, Nordsiek G, Heinrich U, Breuning MH, Ranke MB, Rosenthal A, Ogata T, Rappold GA. Rao E, et al. Among authors: weiss b. Nat Genet. 1997 May;16(1):54-63. doi: 10.1038/ng0597-54. Nat Genet. 1997. PMID: 9140395

5

FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomes.

Rao E, Weiss B, Fukami M, Mertz A, Meder J, Ogata T, Heinrich U, Garcia-Heras J, Schiebel K, Rappold GA. Rao E, et al. Among authors: weiss b. Hum Genet. 1997 Aug;100(2):236-9. doi: 10.1007/s004390050497. Hum Genet. 1997. PMID: 9254856

6

Molecular and evolutionary analysis of the growth-controlling region on the human Y chromosome.

Kirsch S, Weiss B, Zumbach K, Rappold G. Kirsch S, et al. Among authors: weiss b. Hum Genet. 2004 Jan;114(2):173-81. doi: 10.1007/s00439-003-1028-z. Epub 2003 Oct 25. Hum Genet. 2004. PMID: 14579146

7

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.

Berkel S, Marshall CR, Weiss B, Howe J, Roeth R, Moog U, Endris V, Roberts W, Szatmari P, Pinto D, Bonin M, Riess A, Engels H, Sprengel R, Scherer SW, Rappold GA. Berkel S, et al. Among authors: weiss b. Nat Genet. 2010 Jun;42(6):489-91. doi: 10.1038/ng.589. Epub 2010 May 16. Nat Genet. 2010. PMID: 20473310

8

Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain.

Chen J, Wildhardt G, Zhong Z, Röth R, Weiss B, Steinberger D, Decker J, Blum WF, Rappold G. Chen J, et al. Among authors: weiss b. J Med Genet. 2009 Dec;46(12):834-9. doi: 10.1136/jmg.2009.067785. Epub 2009 Jul 2. J Med Genet. 2009. PMID: 19578035 Free PMC article.

9

Assignment of a human homolog of the mouse Htr3 receptor gene to chromosome 11q23.1-q23.2.

Weiss B, Mertz A, Schröck E, Koenen M, Rappold G. Weiss B, et al. Genomics. 1995 Sep 1;29(1):304-5. doi: 10.1006/geno.1995.1254. Genomics. 1995. PMID: 8530095 No abstract available.

10

FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY.

Kirsch S, Weiss B, De Rosa M, Ogata T, Lombardi G, Rappold GA. Kirsch S, et al. Among authors: weiss b. J Med Genet. 2000 Aug;37(8):593-9. doi: 10.1136/jmg.37.8.593. J Med Genet. 2000. PMID: 10922386 Free PMC article.

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