Publications by authors named "Thomas F Wienker"

91Publications

An intronic splice site alteration in combination with a large deletion affecting VPS13B (COH1) causes Cohen syndrome.

Eur J Med Genet 2020 Sep 4;63(9):103973. Epub 2020 Jun 4.

Charité - Universitätsmedizin Berlin, Institut für Medizinische Genetik und Humangenetik, Augustenburger Platz 1, 13353, Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2020.103973DOI Listing
September 2020

Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family-The Role of Next Generation Sequencing in Neuromuscular Disorders.

Neuropediatrics 2020 02 18;51(1):72-75. Epub 2019 Oct 18.

Charité-Universitätsmedizin Berlin, Klinik für Pädiatrie mit Schwerpunkt Neurologie, Augustenburger Platz 1, Berlin, Germany.

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http://dx.doi.org/10.1055/s-0039-1695787DOI Listing
February 2020

VarWatch-A stand-alone software tool for variant matching.

PLoS One 2019 25;14(4):e0215618. Epub 2019 Apr 25.

Institute of Medical Informatics and Statistics, Kiel University, University Hospital Schleswig-Holstein, Kiel, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0215618PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6483337PMC
February 2020

[From phenotype to genotype: a glimpse behind the scenes of an unending story].

Dtsch Med Wochenschr 2015 Dec 16;140(25):1920-3. Epub 2015 Dec 16.

Institut Experimental and Clinical Research Center (ECRC), eine gemeinsame Einrichtung des Max-Delbrück-Centrums für Molekulare Medizin (MDC) und der Charité Medizinischen Fakultät, Berlin.

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http://dx.doi.org/10.1055/s-0041-107586DOI Listing
December 2015

Replication of the association between CHRNA4 rs1044396 and harm avoidance in a large population-based sample.

Eur Neuropsychopharmacol 2016 Jan 14;26(1):150-155. Epub 2015 Nov 14.

Department of Psychiatry and Psychotherapy, University of Bonn, Germany; DZNE, German Center for Neurodegenerative Diseases, Bonn, Germany.

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http://dx.doi.org/10.1016/j.euroneuro.2015.11.007DOI Listing
January 2016

Evaluating information content of SNPs for sample-tagging in re-sequencing projects.

Sci Rep 2015 May 15;5:10247. Epub 2015 May 15.

Department of human molecular genetics, Max-Planck Institute for Molecular Genetics, Berlin, 14195, Germany.

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http://dx.doi.org/10.1038/srep10247DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4432563PMC
May 2015

Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems.

Am J Hum Genet 2015 Mar 19;96(3):386-96. Epub 2015 Feb 19.

Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud university medical center, Nijmegen 6500 HB, the Netherlands; Department of Cognitive Neurosciences, Donders Institute for Brain, Cognition, and Behavior, Radboud university medical center, Nijmegen 6500 HB, the Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.01.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375531PMC
March 2015

NDST1 missense mutations in autosomal recessive intellectual disability.

Am J Med Genet A 2014 Nov 14;164A(11):2753-63. Epub 2014 Aug 14.

Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.

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http://dx.doi.org/10.1002/ajmg.a.36723DOI Listing
November 2014

Previously reported new type of autosomal recessive primary microcephaly is caused by compound heterozygous ASPM gene mutations.

Cell Cycle 2014 1;13(10):1650-1. Epub 2014 Apr 1.

Department of Pediatric Neurology; Charité University Medicine Berlin; Berlin, Germany; Institute of Cell Biology and Neurobiology; Charité University Medicine Berlin; Berlin, Germany.

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http://dx.doi.org/10.4161/cc.28706DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4050170PMC
February 2016

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.

Authors:
S Hong Lee Stephan Ripke Benjamin M Neale Stephen V Faraone Shaun M Purcell Roy H Perlis Bryan J Mowry Anita Thapar Michael E Goddard John S Witte Devin Absher Ingrid Agartz Huda Akil Farooq Amin Ole A Andreassen Adebayo Anjorin Richard Anney Verneri Anttila Dan E Arking Philip Asherson Maria H Azevedo Lena Backlund Judith A Badner Anthony J Bailey Tobias Banaschewski Jack D Barchas Michael R Barnes Thomas B Barrett Nicholas Bass Agatino Battaglia Michael Bauer Mònica Bayés Frank Bellivier Sarah E Bergen Wade Berrettini Catalina Betancur Thomas Bettecken Joseph Biederman Elisabeth B Binder Donald W Black Douglas H R Blackwood Cinnamon S Bloss Michael Boehnke Dorret I Boomsma Gerome Breen René Breuer Richard Bruggeman Paul Cormican Nancy G Buccola Jan K Buitelaar William E Bunney Joseph D Buxbaum William F Byerley Enda M Byrne Sian Caesar Wiepke Cahn Rita M Cantor Miguel Casas Aravinda Chakravarti Kimberly Chambert Khalid Choudhury Sven Cichon C Robert Cloninger David A Collier Edwin H Cook Hilary Coon Bru Cormand Aiden Corvin William H Coryell David W Craig Ian W Craig Jennifer Crosbie Michael L Cuccaro David Curtis Darina Czamara Susmita Datta Geraldine Dawson Richard Day Eco J De Geus Franziska Degenhardt Srdjan Djurovic Gary J Donohoe Alysa E Doyle Jubao Duan Frank Dudbridge Eftichia Duketis Richard P Ebstein Howard J Edenberg Josephine Elia Sean Ennis Bruno Etain Ayman Fanous Anne E Farmer I Nicol Ferrier Matthew Flickinger Eric Fombonne Tatiana Foroud Josef Frank Barbara Franke Christine Fraser Robert Freedman Nelson B Freimer Christine M Freitag Marion Friedl Louise Frisén Louise Gallagher Pablo V Gejman Lyudmila Georgieva Elliot S Gershon Daniel H Geschwind Ina Giegling Michael Gill Scott D Gordon Katherine Gordon-Smith Elaine K Green Tiffany A Greenwood Dorothy E Grice Magdalena Gross Detelina Grozeva Weihua Guan Hugh Gurling Lieuwe De Haan Jonathan L Haines Hakon Hakonarson Joachim Hallmayer Steven P Hamilton Marian L Hamshere Thomas F Hansen Annette M Hartmann Martin Hautzinger Andrew C Heath Anjali K Henders Stefan Herms Ian B Hickie Maria Hipolito Susanne Hoefels Peter A Holmans Florian Holsboer Witte J Hoogendijk Jouke-Jan Hottenga Christina M Hultman Vanessa Hus Andrés Ingason Marcus Ising Stéphane Jamain Edward G Jones Ian Jones Lisa Jones Jung-Ying Tzeng Anna K Kähler René S Kahn Radhika Kandaswamy Matthew C Keller James L Kennedy Elaine Kenny Lindsey Kent Yunjung Kim George K Kirov Sabine M Klauck Lambertus Klei James A Knowles Martin A Kohli Daniel L Koller Bettina Konte Ania Korszun Lydia Krabbendam Robert Krasucki Jonna Kuntsi Phoenix Kwan Mikael Landén Niklas Långström Mark Lathrop Jacob Lawrence William B Lawson Marion Leboyer David H Ledbetter Phil H Lee Todd Lencz Klaus-Peter Lesch Douglas F Levinson Cathryn M Lewis Jun Li Paul Lichtenstein Jeffrey A Lieberman Dan-Yu Lin Don H Linszen Chunyu Liu Falk W Lohoff Sandra K Loo Catherine Lord Jennifer K Lowe Susanne Lucae Donald J MacIntyre Pamela A F Madden Elena Maestrini Patrik K E Magnusson Pamela B Mahon Wolfgang Maier Anil K Malhotra Shrikant M Mane Christa L Martin Nicholas G Martin Manuel Mattheisen Keith Matthews Morten Mattingsdal Steven A McCarroll Kevin A McGhee James J McGough Patrick J McGrath Peter McGuffin Melvin G McInnis Andrew McIntosh Rebecca McKinney Alan W McLean Francis J McMahon William M McMahon Andrew McQuillin Helena Medeiros Sarah E Medland Sandra Meier Ingrid Melle Fan Meng Jobst Meyer Christel M Middeldorp Lefkos Middleton Vihra Milanova Ana Miranda Anthony P Monaco Grant W Montgomery Jennifer L Moran Daniel Moreno-De-Luca Gunnar Morken Derek W Morris Eric M Morrow Valentina Moskvina Pierandrea Muglia Thomas W Mühleisen Walter J Muir Bertram Müller-Myhsok Michael Murtha Richard M Myers Inez Myin-Germeys Michael C Neale Stan F Nelson Caroline M Nievergelt Ivan Nikolov Vishwajit Nimgaonkar Willem A Nolen Markus M Nöthen John I Nurnberger Evaristus A Nwulia Dale R Nyholt Colm O'Dushlaine Robert D Oades Ann Olincy Guiomar Oliveira Line Olsen Roel A Ophoff Urban Osby Michael J Owen Aarno Palotie Jeremy R Parr Andrew D Paterson Carlos N Pato Michele T Pato Brenda W Penninx Michele L Pergadia Margaret A Pericak-Vance Benjamin S Pickard Jonathan Pimm Joseph Piven Danielle Posthuma James B Potash Fritz Poustka Peter Propping Vinay Puri Digby J Quested Emma M Quinn Josep Antoni Ramos-Quiroga Henrik B Rasmussen Soumya Raychaudhuri Karola Rehnström Andreas Reif Marta Ribasés John P Rice Marcella Rietschel Kathryn Roeder Herbert Roeyers Lizzy Rossin Aribert Rothenberger Guy Rouleau Douglas Ruderfer Dan Rujescu Alan R Sanders Stephan J Sanders Susan L Santangelo Joseph A Sergeant Russell Schachar Martin Schalling Alan F Schatzberg William A Scheftner Gerard D Schellenberg Stephen W Scherer Nicholas J Schork Thomas G Schulze Johannes Schumacher Markus Schwarz Edward Scolnick Laura J Scott Jianxin Shi Paul D Shilling Stanley I Shyn Jeremy M Silverman Susan L Slager Susan L Smalley Johannes H Smit Erin N Smith Edmund J S Sonuga-Barke David St Clair Matthew State Michael Steffens Hans-Christoph Steinhausen John S Strauss Jana Strohmaier T Scott Stroup James S Sutcliffe Peter Szatmari Szabocls Szelinger Srinivasa Thirumalai Robert C Thompson Alexandre A Todorov Federica Tozzi Jens Treutlein Manfred Uhr Edwin J C G van den Oord Gerard Van Grootheest Jim Van Os Astrid M Vicente Veronica J Vieland John B Vincent Peter M Visscher Christopher A Walsh Thomas H Wassink Stanley J Watson Myrna M Weissman Thomas Werge Thomas F Wienker Ellen M Wijsman Gonneke Willemsen Nigel Williams A Jeremy Willsey Stephanie H Witt Wei Xu Allan H Young Timothy W Yu Stanley Zammit Peter P Zandi Peng Zhang Frans G Zitman Sebastian Zöllner Bernie Devlin John R Kelsoe Pamela Sklar Mark J Daly Michael C O'Donovan Nicholas Craddock Patrick F Sullivan Jordan W Smoller Kenneth S Kendler Naomi R Wray

Nat Genet 2013 Sep 11;45(9):984-94. Epub 2013 Aug 11.

The University of Queensland, Queensland Brain Institute, Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1038/ng.2711DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800159PMC
September 2013

A newly recognized autosomal recessive syndrome affecting neurologic function and vision.

Am J Med Genet A 2013 Jun 30;161A(6):1207-13. Epub 2013 Apr 30.

Division of Pediatric Neurology, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1002/ajmg.a.35850DOI Listing
June 2013

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

Hum Mol Genet 2012 Dec 4;21(24):5359-72. Epub 2012 Sep 4.

Institute for Medical Biometry, Informatic and Epidemiology, University of Bonn, Bonn, Germany.

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http://hmg.oxfordjournals.org/content/21/24/5359.full.pdf
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http://www.hmg.oxfordjournals.org/cgi/doi/10.1093/hmg/dds373
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http://dx.doi.org/10.1093/hmg/dds373DOI Listing
December 2012

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.

Am J Hum Genet 2011 Mar 25;88(3):372-81. Epub 2011 Feb 25.

Institute of Neuroscience and Medicine (INM-1), Structural and Functional Organization of the Brain, Genomic Imaging, Research Center Juelich, Juelich, Germany.

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http://dx.doi.org/10.1016/j.ajhg.2011.01.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3059436PMC
March 2011

Geostatistical inference of main Y-STR-haplotype groups in Europe.

Forensic Sci Int Genet 2011 Mar;5(2):91-4

Institute for Medical Biometry, Informatics and Epidemiology, University of Bonn, Sigmund-Freud-Str. 25, 53105 Bonn, Germany.

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http://dx.doi.org/10.1016/j.fsigen.2010.09.010DOI Listing
March 2011

Spatial assessment of Argentinean genetic admixture with geographical information systems.

Forensic Sci Int Genet 2011 Aug 19;5(4):297-302. Epub 2010 Jun 19.

Institute for Medical Biometry, Informatics and Epidemiology (IMBIE), University of Bonn, Sigmund-Freud Str. 25, 53105 Bonn, Germany.

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http://dx.doi.org/10.1016/j.fsigen.2010.05.003DOI Listing
August 2011

VEGF gene haplotypes are associated with sarcoidosis.

Chest 2010 Jan 9;137(1):156-63. Epub 2009 Sep 9.

Department of Internal Medicine II, Division of Pneumology, University of Bonn, Sigmund-Freud-Str. 25, D-53105 Bonn, Germany.

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http://dx.doi.org/10.1378/chest.09-1003DOI Listing
January 2010

A new sex-specific genetic map of the human pseudoautosomal regions (PAR1 and PAR2).

Hum Hered 2009 11;68(3):192-200. Epub 2009 Jun 11.

Institute for Medical Biometry, Informatics and Epidemiology, University of Bonn, Bonn, Germany.

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https://www.karger.com/Article/FullText/224639
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http://dx.doi.org/10.1159/000224639DOI Listing
September 2009

Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes.

Cerebrovasc Dis 2008 17;26(2):113-9. Epub 2008 Jun 17.

Department of Neurology, Klinikum Mannheim, University of Heidelberg, Mannheim, Germany.

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http://dx.doi.org/10.1159/000139657DOI Listing
October 2008

The human pseudoautosomal regions: a review for genetic epidemiologists.

Eur J Hum Genet 2008 Jul 9;16(7):771-9. Epub 2008 Apr 9.

Institute for Medical Biometry, Informatics, and Epidemiology, University of Bonn, Bonn, Germany.

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http://www.nature.com/articles/ejhg200863
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http://dx.doi.org/10.1038/ejhg.2008.63DOI Listing
July 2008

Increased gallstone risk in humans conferred by common variant of hepatic ATP-binding cassette transporter for cholesterol.

Hepatology 2007 Sep;46(3):793-801

Department of Internal Medicine I, University Hospital Bonn, Bonner Forum Biomedizin, Germany.

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http://dx.doi.org/10.1002/hep.21847DOI Listing
September 2007

Transmission ratio distortion and maternal effects confound the analysis of modulators of cystic fibrosis disease severity on 19q13.

Eur J Hum Genet 2007 Jul 4;15(7):774-8. Epub 2007 Apr 4.

Institute of Medical Biometrics, Informatics and Genetics (IMBIE), University of Bonn, Bonn, Germany.

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http://dx.doi.org/10.1038/sj.ejhg.5201825DOI Listing
July 2007

Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE.

Bioinformatics 2007 Jan 23;23(1):64-70. Epub 2006 Oct 23.

Institute of Medical Biometry and Epidemiology, Philipps University Marburg, 35032 Marburg, Germany.

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http://dx.doi.org/10.1093/bioinformatics/btl539DOI Listing
January 2007

A common origin of the 4143insA ADAMTS13 mutation.

Thromb Haemost 2006 Jul;96(1):3-6

University Medical Center Hamburg-Eppendorf, Department of Pediatric Hematology and Oncology, Martinistrasse 52, D-20246 Hamburg, Germany.

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http://dx.doi.org/10.1160/TH05-12-0817DOI Listing
July 2006

Familial aggregation of alopecia areata.

J Am Acad Dermatol 2006 Apr 23;54(4):627-32. Epub 2006 Jan 23.

Department of Medical Genetics, University Hospital of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1016/j.jaad.2005.12.007DOI Listing
April 2006

Linkage analysis of alcohol dependence using MOD scores.

BMC Genet 2005 Dec 30;6 Suppl 1:S162. Epub 2005 Dec 30.

Institute for Medical Biometry, Informatics, and Epidemiology, University of Bonn, Sigmund-Freud-Strasse 25, 53105 Bonn, Germany.

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http://dx.doi.org/10.1186/1471-2156-6-S1-S162DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866771PMC
December 2005

VKORC1 haplotypes and their impact on the inter-individual and inter-ethnical variability of oral anticoagulation.

Thromb Haemost 2005 Oct;94(4):773-9

Institute of Transfusion Medicine and Immunohaematology, Department of Molecular Haemostasis, DRK Blood Donor Service Baden Wuerttemberg, Hessen, Frankfurt am Main, Germany.

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http://dx.doi.org/10.1160/TH05-04-0290DOI Listing
October 2005

Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder.

Int J Neuropsychopharmacol 2005 Dec 5;8(4):495-504. Epub 2005 Aug 5.

Clinical and Molecular Psychobiology, Department of Psychiatry and Psychotherapy, University of Wuerzburg, Germany.

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http://dx.doi.org/10.1017/S1461145705005821DOI Listing
December 2005

gammaAla82Gly represents a common fibrinogen gamma-chain variant in Caucasians.

Blood Coagul Fibrinolysis 2005 Apr;16(3):205-8

Institute for Transfusion Medicine and Immune Haematology, DRK Blood Donor Service Baden-Württemberg/Hessen, Sandhofstrasse 1, D-60528 Frankfurt am Main, Germany.

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http://dx.doi.org/10.1097/01.mbc.0000164430.98169.c6DOI Listing
April 2005

A recoding scheme for X-linked and pseudoautosomal loci to be used with computer programs for autosomal LOD-score analysis.

Hum Hered 2004 ;58(1):55-8

Institute for Medical Biometry, Informatics, and Epidemiology, University of Bonn, Bonn, Germany.

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https://www.karger.com/Article/FullText/81457
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http://dx.doi.org/10.1159/000081457DOI Listing
December 2005

Multilocus haplotype analyses reveal association between 5 novel IL-15 polymorphisms and asthma.

J Allergy Clin Immunol 2004 May;113(5):896-901

University Children's Hospital, University of Freiburg, Mathildenstrasse 1, 79106 Freiburg, Germany.

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http://dx.doi.org/10.1016/j.jaci.2004.03.004DOI Listing
May 2004

How to model a complex trait. 2. Analysis with two disease loci.

Hum Hered 2003 ;56(4):200-11

Institute for Medical Biometry, Informatics, and Epidemiology, University of Bonn, Sigmund-Freud-Strasse 25, DE-53105 Bonn, Germany.

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http://dx.doi.org/10.1159/000076394DOI Listing
November 2004

How to model a complex trait. 1. General considerations and suggestions.

Hum Hered 2003 ;55(4):202-10

Institute for Medical Biometry, Informatics, and Epidemiology, University of Bonn, Bonn, Germany.

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https://www.karger.com/Article/FullText/73204
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http://dx.doi.org/10.1159/000073204DOI Listing
June 2004

No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.

Hum Genet 2003 Dec 25;114(1):115-7. Epub 2003 Sep 25.

Institute of Human Genetics, University of Bonn, Wilhelmstrasse 31, 53111 Bonn, Germany.

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http://dx.doi.org/10.1007/s00439-003-1022-5DOI Listing
December 2003

Quantitative analyses of SMN1 and SMN2 based on real-time lightCycler PCR: fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy.

Am J Hum Genet 2002 Feb 21;70(2):358-68. Epub 2001 Dec 21.

Institute of Human Genetics, University Clinic, Rheinische Friedrich-Wilhelms University Bonn, Bonn, Germany.

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http://dx.doi.org/10.1086/338627DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC419987PMC
February 2002

Dermatoglyphic patterns and pattern intensities of the genus Cacajao (Cebidae, platyrrhini) with observations on interspecific and subspecific differentiation.

Am J Primatol 1989 ;19(1):25-37

Publications Editor, Regional Primate Research Center SJ-50, University of Washington, Seattle, WA 98195.

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http://dx.doi.org/10.1002/ajp.1350190104DOI Listing
January 1989