Beckmann JS - Search Results

1

The Réunion paradox and the digenic model.

Beckmann JS. Beckmann JS. Am J Hum Genet. 1996 Dec;59(6):1400-2. Am J Hum Genet. 1996. PMID: 8940289 Free PMC article. No abstract available.

2

A highly significant association between a COMT haplotype and schizophrenia.

Shifman S, Bronstein M, Sternfeld M, Pisanté-Shalom A, Lev-Lehman E, Weizman A, Reznik I, Spivak B, Grisaru N, Karp L, Schiffer R, Kotler M, Strous RD, Swartz-Vanetik M, Knobler HY, Shinar E, Beckmann JS, Yakir B, Risch N, Zak NB, Darvasi A. Shifman S, et al. Among authors: beckmann js. Am J Hum Genet. 2002 Dec;71(6):1296-302. doi: 10.1086/344514. Epub 2002 Oct 25. Am J Hum Genet. 2002. PMID: 12402217 Free PMC article.

3

A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders.

Jacquemont S, Coe BP, Hersch M, Duyzend MH, Krumm N, Bergmann S, Beckmann JS, Rosenfeld JA, Eichler EE. Jacquemont S, et al. Among authors: beckmann js. Am J Hum Genet. 2014 Mar 6;94(3):415-25. doi: 10.1016/j.ajhg.2014.02.001. Epub 2014 Feb 27. Am J Hum Genet. 2014. PMID: 24581740 Free PMC article.

4

On the applicability of a haplotype map to un-assayed populations.

Pe'er I, Beckmann JS. Pe'er I, et al. Among authors: beckmann js. Hum Genet. 2004 Jan;114(2):214-7. doi: 10.1007/s00439-003-1046-x. Epub 2003 Oct 25. Hum Genet. 2004. PMID: 14579151 Review.

5

Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus.

Belal S, Panayides K, Sirugo G, Ben Hamida C, Ioannou P, Hentati F, Beckmann J, Koenig M, Mandel JL, Ben Hamida M, et al. Belal S, et al. Am J Hum Genet. 1992 Dec;51(6):1372-6. Am J Hum Genet. 1992. PMID: 1463017 Free PMC article.

6

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.

Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Crétien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rössler J, Le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H. Dgany O, et al. Among authors: beckmann js. Am J Hum Genet. 2002 Dec;71(6):1467-74. doi: 10.1086/344781. Epub 2002 Nov 14. Am J Hum Genet. 2002. PMID: 12434312 Free PMC article.

7

Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval.

Levi A, Kohn Y, Kanyas K, Amann D, Pae CU, Hamdan A, Segman RH, Avidan N, Karni O, Korner M, Jun TY, Beckmann JS, Macciardi F, Lerer B. Levi A, et al. Among authors: beckmann js. Eur J Hum Genet. 2005 Jun;13(6):763-71. doi: 10.1038/sj.ejhg.5201406. Eur J Hum Genet. 2005. PMID: 15812564

8

Recovering frequencies of known haplotype blocks from single-nucleotide polymorphism allele frequencies.

Pe'er I, Beckmann JS. Pe'er I, et al. Among authors: beckmann js. Genetics. 2004 Apr;166(4):2001-6. doi: 10.1534/genetics.166.4.2001. Genetics. 2004. PMID: 15126415 Free PMC article.

9

AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia.

Amann-Zalcenstein D, Avidan N, Kanyas K, Ebstein RP, Kohn Y, Hamdan A, Ben-Asher E, Karni O, Mujaheed M, Segman RH, Maier W, Macciardi F, Beckmann JS, Lancet D, Lerer B. Amann-Zalcenstein D, et al. Among authors: beckmann js. Eur J Hum Genet. 2006 Oct;14(10):1111-9. doi: 10.1038/sj.ejhg.5201675. Epub 2006 Jun 14. Eur J Hum Genet. 2006. PMID: 16773125

10

The association of DNA sequence variation at the MAOA genetic locus with quantitative behavioural traits in normal males.

Rosenberg S, Templeton AR, Feigin PD, Lancet D, Beckmann JS, Selig S, Hamer DH, Skorecki K. Rosenberg S, et al. Among authors: beckmann js. Hum Genet. 2006 Nov;120(4):447-59. doi: 10.1007/s00439-006-0198-x. Epub 2006 Aug 2. Hum Genet. 2006. PMID: 16896926

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