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CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT).
Nephrol Dial Transplant. 2012 Jun;27(6):2355-64. doi: 10.1093/ndt/gfr649. Epub 2011 Dec 6.
Nephrol Dial Transplant. 2012.
PMID: 22146311
Free article.
Neurologic and ocular phenotype in Pitt-Hopkins syndrome and a zebrafish model.
Brockschmidt A, Filippi A, Charbel Issa P, Nelles M, Urbach H, Eter N, Driever W, Weber RG.
Brockschmidt A, et al.
Hum Genet. 2011 Nov;130(5):645-55. doi: 10.1007/s00439-011-0999-4. Epub 2011 May 5.
Hum Genet. 2011.
PMID: 21544580
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DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation.
Engels H, Brockschmidt A, Hoischen A, Landwehr C, Bosse K, Walldorf C, Toedt G, Radlwimmer B, Propping P, Lichter P, Weber RG.
Engels H, et al. Among authors: brockschmidt a.
Neurology. 2007 Mar 6;68(10):743-50. doi: 10.1212/01.wnl.0000256367.70365.e0.
Neurology. 2007.
PMID: 17339581
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KIAA1797/FOCAD encodes a novel focal adhesion protein with tumour suppressor function in gliomas.
Brockschmidt A, Trost D, Peterziel H, Zimmermann K, Ehrler M, Grassmann H, Pfenning PN, Waha A, Wohlleber D, Brockschmidt FF, Jugold M, Hoischen A, Kalla C, Waha A, Seifert G, Knolle PA, Latz E, Hans VH, Wick W, Pfeifer A, Angel P, Weber RG.
Brockschmidt A, et al.
Brain. 2012 Apr;135(Pt 4):1027-41. doi: 10.1093/brain/aws045. Epub 2012 Mar 16.
Brain. 2012.
PMID: 22427331
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Severe mental retardation with breathing abnormalities (Pitt-Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4.
Brockschmidt A, Todt U, Ryu S, Hoischen A, Landwehr C, Birnbaum S, Frenck W, Radlwimmer B, Lichter P, Engels H, Driever W, Kubisch C, Weber RG.
Brockschmidt A, et al.
Hum Mol Genet. 2007 Jun 15;16(12):1488-94. doi: 10.1093/hmg/ddm099. Epub 2007 May 3.
Hum Mol Genet. 2007.
PMID: 17478476
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A phenotype map for 14q32.3 terminal deletions.
Engels H, Schüler HM, Zink AM, Wohlleber E, Brockschmidt A, Hoischen A, Drechsler M, Lee JA, Ludwig KU, Kubisch C, Schwanitz G, Weber RG, Leube B, Hennekam RC, Rudnik-Schöneborn S, Kreiss-Nachtsheim M, Reutter H.
Engels H, et al. Among authors: brockschmidt a.
Am J Med Genet A. 2012 Apr;158A(4):695-706. doi: 10.1002/ajmg.a.35256. Epub 2012 Feb 24.
Am J Med Genet A. 2012.
PMID: 22367666
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Precision oncology for intrahepatic cholangiocarcinoma in clinical practice.
Tomczak A, Springfeld C, Dill MT, Chang DH, Kazdal D, Wagner U, Mehrabi A, Brockschmidt A, Luedde T, Naumann P, Stenzinger A, Schirmacher P, Longerich T.
Tomczak A, et al. Among authors: brockschmidt a.
Br J Cancer. 2022 Nov;127(9):1701-1708. doi: 10.1038/s41416-022-01932-1. Epub 2022 Aug 19.
Br J Cancer. 2022.
PMID: 35986087
Free PMC article.
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