Propping P - Search Results

1

Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease.

Betz RC, Schoser BG, Kasper D, Ricker K, Ramírez A, Stein V, Torbergsen T, Lee YA, Nöthen MM, Wienker TF, Malin JP, Propping P, Reis A, Mortier W, Jentsch TJ, Vorgerd M, Kubisch C. Betz RC, et al. Among authors: propping p. Nat Genet. 2001 Jul;28(3):218-9. doi: 10.1038/90050. Nat Genet. 2001. PMID: 11431690

2

Susceptibility variants for male-pattern baldness on chromosome 20p11.

Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms S, Becker T, Kortüm AK, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Mühleisen TW, Alblas MA, Moebus S, Jöckel KH, Bröcker-Preuss M, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Nöthen MM. Hillmer AM, et al. Among authors: propping p. Nat Genet. 2008 Nov;40(11):1279-81. doi: 10.1038/ng.228. Epub 2008 Oct 12. Nat Genet. 2008. PMID: 18849994

3

Association versus linkage studies in psychosis genetics.

Nöthen MM, Propping P, Fimmers R. Nöthen MM, et al. Among authors: propping p. J Med Genet. 1993 Aug;30(8):634-7. doi: 10.1136/jmg.30.8.634. J Med Genet. 1993. PMID: 8411047 Free PMC article. No abstract available.

4

A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.

Betz RC, Lee YA, Bygum A, Brandrup F, Bernal AI, Toribio J, Alvarez JI, Kukuk GM, Ibsen HH, Rasmussen HB, Wienker TF, Reis A, Propping P, Kruse R, Cichon S, Nöthen MM. Betz RC, et al. Among authors: propping p. Am J Hum Genet. 2000 Jun;66(6):1979-83. doi: 10.1086/302934. Epub 2000 May 2. Am J Hum Genet. 2000. PMID: 10793007 Free PMC article.

5

Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.

Bosse K, Betz RC, Lee YA, Wienker TF, Reis A, Kleen H, Propping P, Cichon S, Nöthen MM. Bosse K, et al. Among authors: propping p. Am J Hum Genet. 2000 Aug;67(2):492-7. doi: 10.1086/303028. Epub 2000 Jun 30. Am J Hum Genet. 2000. PMID: 10877983 Free PMC article.

6

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

Birnbaum S, Ludwig KU, Reutter H, Herms S, Steffens M, Rubini M, Baluardo C, Ferrian M, Almeida de Assis N, Alblas MA, Barth S, Freudenberg J, Lauster C, Schmidt G, Scheer M, Braumann B, Bergé SJ, Reich RH, Schiefke F, Hemprich A, Pötzsch S, Steegers-Theunissen RP, Pötzsch B, Moebus S, Horsthemke B, Kramer FJ, Wienker TF, Mossey PA, Propping P, Cichon S, Hoffmann P, Knapp M, Nöthen MM, Mangold E. Birnbaum S, et al. Among authors: propping p. Nat Genet. 2009 Apr;41(4):473-7. doi: 10.1038/ng.333. Epub 2009 Mar 8. Nat Genet. 2009. PMID: 19270707

7

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.

Haug K, Warnstedt M, Alekov AK, Sander T, Ramírez A, Poser B, Maljevic S, Hebeisen S, Kubisch C, Rebstock J, Horvath S, Hallmann K, Dullinger JS, Rau B, Haverkamp F, Beyenburg S, Schulz H, Janz D, Giese B, Müller-Newen G, Propping P, Elger CE, Fahlke C, Lerche H, Heils A. Haug K, et al. Among authors: propping p. Nat Genet. 2003 Apr;33(4):527-32. doi: 10.1038/ng1121. Epub 2003 Mar 3. Nat Genet. 2003. Retraction in: Nat Genet. 2009 Sep;41(9):1043. doi: 10.1038/ng0909-1043 PMID: 12612585 Retracted.

8

Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1).

Cichon S, Nöthen MM, Erdmann J, Propping P. Cichon S, et al. Among authors: propping p. Hum Mol Genet. 1994 Jan;3(1):209. doi: 10.1093/hmg/3.1.209. Hum Mol Genet. 1994. PMID: 8162032 No abstract available.

9

Genetic variation of CNS receptors--a new perspective for pharmacogenetics.

Propping P, Nöthen MM. Propping P, et al. Pharmacogenetics. 1995 Oct;5(5):318-25. doi: 10.1097/00008571-199510000-00008. Pharmacogenetics. 1995. PMID: 8563773 Review. No abstract available.

10

Lack of imprinting of the human dopamine D4 receptor (DRD4) gene.

Cichon S, Nöthen MM, Wolf HK, Propping P. Cichon S, et al. Among authors: propping p. Am J Med Genet. 1996 Apr 9;67(2):229-31. doi: 10.1002/(SICI)1096-8628(19960409)67:2<229::AID-AJMG17>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8723054

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