Klauck SM - Search Results

1

A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations.

Mikati MA, Maguire H, Barlow CF, Ozelius L, Breakefield XO, Klauck SM, Korf B, O'Tuama SL, Dangond F. Mikati MA, et al. Among authors: klauck sm. Neurology. 1992 Dec;42(12):2251-7. doi: 10.1212/wnl.42.12.2251. Neurology. 1992. PMID: 1361034

2

Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease.

Seizinger BR, Smith DI, Filling-Katz MR, Neumann H, Green JS, Choyke PL, Anderson KM, Freiman RN, Klauck SM, Whaley J, et al. Seizinger BR, et al. Among authors: klauck sm. Proc Natl Acad Sci U S A. 1991 Apr 1;88(7):2864-8. doi: 10.1073/pnas.88.7.2864. Proc Natl Acad Sci U S A. 1991. PMID: 2011596 Free PMC article.

3

Cytogenetic and fluorescence in situ hybridization studies on sporadic and hereditary tumors associated with von Hippel-Lindau syndrome (VHL).

Decker HJ, Klauck SM, Lawrence JB, McNeil J, Smith D, Gemmill RM, Sandberg AA, Neumann HH, Simon B, Green J, et al. Decker HJ, et al. Among authors: klauck sm. Cancer Genet Cytogenet. 1994 Oct;77(1):1-13. doi: 10.1016/0165-4608(94)90141-4. Cancer Genet Cytogenet. 1994. PMID: 7923076

4

A genome-wide linkage and association scan reveals novel loci for autism.

Weiss LA, Arking DE; Gene Discovery Project of Johns Hopkins & the Autism Consortium; Daly MJ, Chakravarti A. Weiss LA, et al. Nature. 2009 Oct 8;461(7265):802-8. doi: 10.1038/nature08490. Nature. 2009. PMID: 19812673 Free PMC article.

5

Cytogenetic and molecular studies of a familial renal cell carcinoma.

Decker HJ, Wullich B, Whaley JM, Herrera G, Klauck SM, Sandberg AA, Yandell DW, Seizinger BR. Decker HJ, et al. Among authors: klauck sm. Cancer Genet Cytogenet. 1992 Oct 1;63(1):25-31. doi: 10.1016/0165-4608(92)90059-h. Cancer Genet Cytogenet. 1992. PMID: 1423222

6

Dinucleotide repeat polymorphism at the D3S1255 locus.

Klauck SM, Whisenant E, Wood M, Drabkin HA, Seizinger BR. Klauck SM, et al. Hum Mol Genet. 1994 May;3(5):840. Hum Mol Genet. 1994. PMID: 8081378 No abstract available.

7

Dinucleotide repeat polymorphism at the D3S666 locus.

Klauck SM, Yamakawa K, Seizinger BR. Klauck SM, et al. Hum Mol Genet. 1994 May;3(5):840. Hum Mol Genet. 1994. PMID: 8081379 No abstract available.

8

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.

Weiner DJ, Wigdor EM, Ripke S, Walters RK, Kosmicki JA, Grove J, Samocha KE, Goldstein JI, Okbay A, Bybjerg-Grauholm J, Werge T, Hougaard DM, Taylor J; iPSYCH-Broad Autism Group; Psychiatric Genomics Consortium Autism Group; Skuse D, Devlin B, Anney R, Sanders SJ, Bishop S, Mortensen PB, Børglum AD, Smith GD, Daly MJ, Robinson EB. Weiner DJ, et al. Nat Genet. 2017 Jul;49(7):978-985. doi: 10.1038/ng.3863. Epub 2017 May 15. Nat Genet. 2017. PMID: 28504703 Free PMC article.

9

Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.

Liu XQ, Paterson AD, Szatmari P; Autism Genome Project Consortium. Liu XQ, et al. Biol Psychiatry. 2008 Oct 1;64(7):561-70. doi: 10.1016/j.biopsych.2008.05.023. Epub 2008 Jul 16. Biol Psychiatry. 2008. PMID: 18632090 Free PMC article.

10

Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder.

Maier R, Moser G, Chen GB, Ripke S; Cross-Disorder Working Group of the Psychiatric Genomics Consortium; Coryell W, Potash JB, Scheftner WA, Shi J, Weissman MM, Hultman CM, Landén M, Levinson DF, Kendler KS, Smoller JW, Wray NR, Lee SH. Maier R, et al. Am J Hum Genet. 2015 Feb 5;96(2):283-94. doi: 10.1016/j.ajhg.2014.12.006. Epub 2015 Jan 29. Am J Hum Genet. 2015. PMID: 25640677 Free PMC article.

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