Müller-Myhsok B - Search Results

1

Robustness and power of the maximum-likelihood-binomial and maximum-likelihood-score methods, in multipoint linkage analysis of affected-sibship data.

Abel L, Müller-Myhsok B. Abel L, et al. Am J Hum Genet. 1998 Aug;63(2):638-47. doi: 10.1086/301958. Am J Hum Genet. 1998. PMID: 9683590 Free PMC article.

2

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

Gasser T, Müller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V, Bereznai B, Fabrizio E, Vieregge P, Horstmann RD. Gasser T, et al. Nat Genet. 1998 Mar;18(3):262-5. doi: 10.1038/ng0398-262. Nat Genet. 1998. PMID: 9500549

3

hSKCa3: a candidate gene for schizophrenia?

Meissner B, Purmann S, Schürmann M, Zühlke C, Lencer R, Arolt V, Müller-Myhsok B, Morris-Rosendahl DJ, Schwinger E. Meissner B, et al. Psychiatr Genet. 1999 Jun;9(2):91-6. Psychiatr Genet. 1999. PMID: 10412188

4

An extensive comparison of quantitative trait Loci mapping methods.

Kleensang A, Franke D, Alcaïs A, Abel L, Müller-Myhsok B, Ziegler A. Kleensang A, et al. Hum Hered. 2010;69(3):202-11. doi: 10.1159/000289596. Epub 2010 Mar 5. Hum Hered. 2010. PMID: 20203525

5

Rapid simulation of P values for product methods and multiple-testing adjustment in association studies.

Seaman SR, Müller-Myhsok B. Seaman SR, et al. Am J Hum Genet. 2005 Mar;76(3):399-408. doi: 10.1086/428140. Epub 2005 Jan 11. Am J Hum Genet. 2005. PMID: 15645388 Free PMC article.

6

A cholesterol-lowering gene maps to chromosome 13q.

Knoblauch H, Müller-Myhsok B, Busjahn A, Ben Avi L, Bähring S, Baron H, Heath SC, Uhlmann R, Faulhaber HD, Shpitzen S, Aydin A, Reshef A, Rosenthal M, Eliav O, Mühl A, Lowe A, Schurr D, Harats D, Jeschke E, Friedlander Y, Schuster H, Luft FC, Leitersdorf E. Knoblauch H, et al. Am J Hum Genet. 2000 Jan;66(1):157-66. doi: 10.1086/302704. Am J Hum Genet. 2000. PMID: 10631147 Free PMC article.

7

Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia.

Arolt V, Lencer R, Purmann S, Schürmann M, Müller-Myhsok B, Krecker K, Schwinger E. Arolt V, et al. Am J Med Genet. 1999 Dec 15;88(6):603-6. Am J Med Genet. 1999. PMID: 10581476 No abstract available.

8

Maximum-likelihood expression of the transmission/disequilibrium test and power considerations.

Abel L, Müller-Myhsok B. Abel L, et al. Am J Hum Genet. 1998 Aug;63(2):664-7. doi: 10.1086/301975. Am J Hum Genet. 1998. PMID: 9683606 Free PMC article. No abstract available.

9

Further evidence suggesting the presence of a locus, on human chromosome 5q31-q33, influencing the intensity of infection with Schistosoma mansoni.

Müller-Myhsok B, Stelma FF, Guissé-Sow F, Muntau B, Thye T, Burchard GD, Gryseels B, Horstmann RD. Müller-Myhsok B, et al. Am J Hum Genet. 1997 Aug;61(2):452-4. doi: 10.1016/S0002-9297(07)64073-7. Am J Hum Genet. 1997. PMID: 9311752 Free PMC article. No abstract available.

10

Evidence for linkage of spelling disability to chromosome 15.

Schulte-Körne G, Grimm T, Nöthen MM, Müller-Myhsok B, Cichon S, Vogt IR, Propping P, Remschmidt H. Schulte-Körne G, et al. Am J Hum Genet. 1998 Jul;63(1):279-82. doi: 10.1086/301919. Am J Hum Genet. 1998. PMID: 9634517 Free PMC article. No abstract available.

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