Knapp M - Search Results

1

Strong association of variants around FOXE1 and orofacial clefting.

Ludwig KU, Böhmer AC, Rubini M, Mossey PA, Herms S, Nowak S, Reutter H, Alblas MA, Lippke B, Barth S, Paredes-Zenteno M, Muñoz-Jimenez SG, Ortiz-Lopez R, Kreusch T, Hemprich A, Martini M, Braumann B, Jäger A, Pötzsch B, Molloy A, Peterlin B, Hoffmann P, Nöthen MM, Rojas-Martinez A, Knapp M, Steegers-Theunissen RP, Mangold E. Ludwig KU, et al. Among authors: knapp m. J Dent Res. 2014 Apr;93(4):376-81. doi: 10.1177/0022034514523987. Epub 2014 Feb 21. J Dent Res. 2014. PMID: 24563486

2

Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing.

Hoebel AK, Drichel D, van de Vorst M, Böhmer AC, Sivalingam S, Ishorst N, Klamt J, Gölz L, Alblas M, Maaser A, Keppler K, Zink AM, Dixon MJ, Dixon J, Hemprich A, Kruse T, Graf I, Dunsche A, Schmidt G, Daratsianos N, Nowak S, Aldhorae KA, Nöthen MM, Knapp M, Thiele H, Gilissen C, Reutter H, Hoischen A, Mangold E, Ludwig KU. Hoebel AK, et al. Among authors: knapp m. J Dent Res. 2017 Oct;96(11):1314-1321. doi: 10.1177/0022034517722761. Epub 2017 Aug 2. J Dent Res. 2017. PMID: 28767323

3

MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration.

Stüssel LG, Hollstein R, Laugsch M, Hochfeld LM, Welzenbach J, Schröder J, Thieme F, Ishorst N, Romero RO, Weinhold L, Hess T, Gehlen J, Mostowska A, Heilmann-Heimbach S, Mangold E, Rada-Iglesias A, Knapp M, Schaaf CP, Ludwig KU. Stüssel LG, et al. Among authors: knapp m. J Dent Res. 2022 Mar;101(3):323-330. doi: 10.1177/00220345211038203. Epub 2021 Sep 16. J Dent Res. 2022. PMID: 34528480

4

TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palate.

Reutter H, Birnbaum S, Mende M, Lauster C, Schmidt G, Henschke H, Saffar M, Martini M, Lauster R, Schiefke F, Reich RH, Braumann B, Scheer M, Knapp M, Nöthen MM, Kramer FJ, Mangold E. Reutter H, et al. Among authors: knapp m. J Hum Genet. 2008;53(7):656-661. doi: 10.1007/s10038-008-0296-9. Epub 2008 May 15. J Hum Genet. 2008. PMID: 18480962

5

Evidence for a polygenic contribution to androgenetic alopecia.

Heilmann S, Brockschmidt FF, Hillmer AM, Hanneken S, Eigelshoven S, Ludwig KU, Herold C, Mangold E, Becker T, Kruse R, Knapp M, Nöthen MM. Heilmann S, et al. Among authors: knapp m. Br J Dermatol. 2013 Oct;169(4):927-30. doi: 10.1111/bjd.12443. Br J Dermatol. 2013. PMID: 23701444

6

Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate.

Mostowska A, Gaczkowska A, Żukowski K, Ludwig KU, Hozyasz KK, Wójcicki P, Mangold E, Böhmer AC, Heilmann-Heimbach S, Knapp M, Zadurska M, Biedziak B, Budner M, Lasota A, Daktera-Micker A, Jagodziński PP. Mostowska A, et al. Among authors: knapp m. Clin Genet. 2018 Apr;93(4):784-793. doi: 10.1111/cge.13141. Epub 2018 Feb 11. Clin Genet. 2018. PMID: 28926086

7

Human 5-HT5A receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5' untranslated region.

Shimron-Abarbanell D, Erdmann J, Vogt IR, Bryant SP, Spurr NK, Knapp M, Propping P, Nöthen MM. Shimron-Abarbanell D, et al. Among authors: knapp m. Biochem Biophys Res Commun. 1997 Apr 7;233(1):6-9. doi: 10.1006/bbrc.1997.6390. Biochem Biophys Res Commun. 1997. PMID: 9144385

8

Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophrenia.

Erdmann J, Shimron-Abarbanell D, Rietschel M, Albus M, Maier W, Körner J, Bondy B, Chen K, Shih JC, Knapp M, Propping P, Nöthen MM. Erdmann J, et al. Among authors: knapp m. Hum Genet. 1996 May;97(5):614-9. doi: 10.1007/BF02281871. Hum Genet. 1996. PMID: 8655141

9

DRD4 exon III VNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach.

Franke P, Nöthen MM, Wang T, Knapp M, Lichtermann D, Neidt H, Sander T, Propping P, Maier W. Franke P, et al. Among authors: knapp m. Mol Psychiatry. 2000 Jan;5(1):101-4. doi: 10.1038/sj.mp.4000583. Mol Psychiatry. 2000. PMID: 10673776

10

Investigation of the human serotonin 6 [5-HT6] receptor gene in bipolar affective disorder and schizophrenia.

Vogt IR, Shimron-Abarbanell D, Neidt H, Erdmann J, Cichon S, Schulze TG, Müller DJ, Maier W, Albus M, Borrmann-Hassenbach M, Knapp M, Rietschel M, Propping P, Nöthen MM. Vogt IR, et al. Among authors: knapp m. Am J Med Genet. 2000 Apr 3;96(2):217-21. Am J Med Genet. 2000. PMID: 10893499

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