Manfred Stuhrmann

Manfred Stuhrmann

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Manfred Stuhrmann

Manfred Stuhrmann

Publications by authors named "Manfred Stuhrmann"

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Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.

Am J Psychiatry 2019 Mar;176(3):217-227

The Psychiatric and Neurodevelopmental Genetics Unit, Center for Genomic Medicine, Department of Psychiatry, Massachusetts General Hospital, Boston (Yu, Illmann, Osiecki, Smoller, Pauls, Neale, Scharf); the Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Mass. (Yu, Neale, Scharf); the Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles (Sul, Huang, Zelaya, Ophoff, Freimer, Coppola); the Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles (Sul, Huang, Zelaya, Freimer, Coppola); the Department of Molecular Biology and Genetics, Democritus University of Thrace, Xanthi, Greece (Tsetsos); the Department of Biological Sciences, Purdue University, West Lafayette, Ind. (Tsetsos, Paschou); deCODE Genetics/Amgen, Reykjavik, Iceland (Nawaz, H. Stefansson, K. Stefansson); the Bioinformatics Interdepartmental Program, University of California, Los Angeles (Huang, Zelaya); the Department of Psychiatry, University of California, San Francisco (Darrow); the Department of Psychiatry, UCSF Weill Institute for Neurosciences, University of California, San Francisco (Hirschtritt, Willsey); the Department of Psychiatry, Massachusetts General Hospital, Boston (Greenberg, Roffman, Buckner); the Clinic of Psychiatry, Social Psychiatry, and Psychotherapy, Hannover Medical School, Hannover, Germany (Muller-Vahl); the Institute of Human Genetics, Hannover Medical School, Hannover, Germany (Stuhrmann); McGill University Health Center, University of Montreal, McGill University Health Centre, Montreal (Dion); the Montreal Neurological Institute, Department of Neurology and Neurosurgery, McGill University, Montreal (Rouleau); the Department of Psychiatry and Psychotherapy, Medical University Vienna, Vienna (Aschauer, Stamenkovic); Biopsychosocial Corporation, Vienna (Aschauer, Schlögelhofer); University Health Network, Youthdale Treatment Centres, and University of Toronto, Toronto (Sandor); the Krembil Research Institute, University Health Network, Hospital for Sick Children, and University of Toronto, Toronto (Barr); Johns Hopkins University School of Medicine, Baltimore (Grados, Singer); the Institute of Human Genetics, University Hospital Bonn, University of Bonn Medical School, Bonn, Germany (Nöthen); the Department of Child and Adolescent Psychiatry, Psychosomatics, and Psychotherapy, University Hospital Essen, University of Duisburg-Essen, Essen, Germany (Hebebrand, Hinney); the Yale Child Study Center and the Department of Psychiatry, Yale University School of Medicine, New Haven, Conn. (King, Fernandez); the Institute of Medical Chemistry, Molecular Biology, and Pathobiochemistry, Semmelweis University, Budapest, Hungary (Barta); Vadaskert Child and Adolescent Psychiatric Hospital, Budapest, Hungary (Tarnok, Nagy); the Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany (Depienne); Sorbonne Universités, UPMC Université Paris 06, UMR S 1127, CNRS UMR 7225, ICM, Paris (Depienne, Worbe, Hartmann); French Reference Centre for Gilles de la Tourette Syndrome, Groupe Hospitalier Pitié-Salpêtrière, Paris (Worbe, Hartmann); Assistance Publique-Hôpitaux de Paris, Department of Neurology, Groupe Hospitalier Pitié-Salpêtrière, Paris (Worbe, Hartmann); Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York (Budman); Child Neuropsychiatry, Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy (Rizzo); the Stanley Institute for Cognitive Genomics, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York (Lyon); the Department of Psychiatry, University of Utah, Salt Lake City (McMahon); Children's Mercy Hospital, Kansas City, Mo. (Batterson); the Department of Psychiatry, University Medical Center Groningen and Rijksuniversity Groningen, and Drenthe Mental Health Center, Groningen, the Netherlands (Cath); the Department of Neurology, Fixel Center for Neurological Diseases, McKnight Brain Institute, University of Florida, Gainesville (Malaty, Okun); Pennsylvania State University College of Medicine, Hershey (Berlin); Marquette University and University of Wisconsin-Milwaukee, Milwaukee (Woods); Tripler Army Medical Center and University of Hawaii John A. Burns School of Medicine, Honolulu (Lee); Parkinson's Disease Center and Movement Disorders Clinic, Department of Neurology, Baylor College of Medicine, Houston (Jankovic); the Division of Psychiatry, Department of Neuropsychiatry, University College London (Robertson); the Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati (Gilbert); Children's Hospital of Philadelphia, Philadelphia (Brown); the Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of Medicine, Miami (Coffey); the Department of Child and Adolescent Psychiatry, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands (Dietrich, Hoekstra); University of Iowa Carver College of Medicine, Iowa City (Kuperman); the Department of Pediatrics, University of Washington, Seattle (Zinner); the Department of Pediatrics, Landspitalinn University Hospital, Reykjavik, Iceland (Luðvigsson, Thorarensen); the Faculty of Medicine, University of Iceland, Reykjavík, Iceland (Sæmundsen, Stefansson); the State Diagnostic and Counselling Centre, Kópavogur, Iceland (Sæmundsen); the Department of Genetics and the Department of Medicine, Albert Einstein College of Medicine, Bronx, New York (Atzmon, Barzilai); the Department of Human Biology, Haifa University, Haifa, Israel (Atzmon); the Department of Psychiatry and Psychotherapy, University of Bonn, Bonn, Germany (Wagner); the Department of Psychiatry and Psychotherapy, University of Tübingen, Tübingen, Germany (Moessner); SUNY Downstate Medical Center Brooklyn, New York (C.M. Pato, M.T. Pato, Knowles); the Athinoula A. Martinos Center for Biomedical Research, Department of Radiology, Massachusetts General Hospital, Charlestown (Roffman, Buckner); the Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston (Smoller); the Center for Brain Science and Department of Psychology, Harvard University, Cambridge, Mass. (Buckner); the Institute for Neurodegenerative Diseases, UCSF Weill Institute for Neurosciences, University of California San Francisco, San Francisco (Willsey); the Department of Genetics and the Human Genetics Institute of New Jersey, Rutgers, the State University of New Jersey, Piscataway (Tischfield, Heiman); the Department of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, VU University Amsterdam, Amsterdam (Posthuma); the Division of Genetic Medicine, Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, Tenn. (Cox, Davis); the Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston (Neale); the Department of Psychiatry, Genetics Institute, University of Florida, Gainesville (Mathews); and the Department of Neurology, Brigham and Women's Hospital, and the Department of Neurology, Massachusetts General Hospital, Boston (Scharf).

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http://dx.doi.org/10.1176/appi.ajp.2018.18070857DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6677250PMC
March 2019

NCAM2 deletion in a boy with macrocephaly and autism: Cause, association or predisposition?

Eur J Med Genet 2016 Oct 2;59(10):493-8. Epub 2016 Sep 2.

Institute of Human Genetics, Hannover Medical School, Hannover, Germany.

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http://dx.doi.org/10.1016/j.ejmg.2016.08.006DOI Listing
October 2016

Blood-based microRNA signatures differentiate various forms of cardiac hypertrophy.

Int J Cardiol 2015 Oct 5;196:115-22. Epub 2015 Jun 5.

Institute of Molecular and Translational Therapeutic Strategies (IMTTS), IFB-Tx, Hannover Medical School, Hannover, Germany; Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany; National Heart and Lung Institute, Imperial College London, UK. Electronic address:

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http://dx.doi.org/10.1016/j.ijcard.2015.05.185DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936391PMC
October 2015

Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland.

Mol Cell Probes 2015 Feb 4;29(1):31-4. Epub 2014 Nov 4.

Institute for Human Genetics, Hannover Medical School, Carl-Neuberg Str.1, D-30625 Hannover, Germany.

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http://dx.doi.org/10.1016/j.mcp.2014.10.006DOI Listing
February 2015

CFTR, SPINK1, PRSS1, and CTRC mutations are not associated with pancreatic cancer in German patients.

Pancreas 2014 Oct;43(7):1078-82

From the Institutes of *Human Genetics and †Pathology, Hannover Medical School, Hannover, Germany; ‡Department of Andrology, University Hospital Hamburg-Eppendorf, Hamburg, Germany; and §Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.

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http://dx.doi.org/10.1097/MPA.0000000000000166DOI Listing
October 2014

1,25-Dihydroxyvitamin D decreases HTRA1 promoter activity in the rhesus monkey--a plausible explanation for the influence of vitamin D on age-related macular degeneration?

Exp Eye Res 2013 Nov 27;116:234-9. Epub 2013 Sep 27.

Institute of Human Genetics, Hannover Medical School, Hannover, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.exer.2013.09.012DOI Listing
November 2013

Improvement of interpretation in cystic fibrosis clinical laboratory reports: longitudinal analysis of external quality assessment data.

Eur J Hum Genet 2012 Dec 20;20(12):1209-15. Epub 2012 Jun 20.

Department of Public Health, Biomedical Quality Assurance Research Unit, Katholieke Universiteit Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2012.131DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499747PMC
December 2012

Diagnosis of hereditary hemochromatosis in the era of genetic testing.

Dig Dis Sci 2012 Nov 7;57(11):2988-94. Epub 2012 Jun 7.

Department of Internal Medicine I, University Hospital Ulm, Ulm, Germany.

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http://dx.doi.org/10.1007/s10620-012-2243-zDOI Listing
November 2012

A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?

Neuropediatrics 2012 Jun 19;43(3):159-61. Epub 2012 May 19.

Istanbul University, Cerrahpasa Medical Faculty, Department of Neurology, Division of Child Neurology, Istanbul, Turkey.

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http://dx.doi.org/10.1055/s-0032-1313912DOI Listing
June 2012

Characterization of the 10q26-orthologue in rhesus monkeys corroborates a functional connection between ARMS2 and HTRA1.

Exp Eye Res 2012 May 21;98:75-8. Epub 2012 Mar 21.

Institute of Human Genetics, Hannover Medical School, OE 6300, Carl-Neuberg-Str. 1, D-30625 Hannover, Germany.

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http://dx.doi.org/10.1016/j.exer.2012.03.007DOI Listing
May 2012

Are polymorphisms of molecules involved in bone healing correlated to aseptic femoral and tibial shaft non-unions?

J Orthop Res 2011 Nov 28;29(11):1724-31. Epub 2011 Apr 28.

Trauma Department, Hannover Medical School, Carl-Neuberg-Street 1, 30625 Hannover, Germany.

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http://dx.doi.org/10.1002/jor.21443DOI Listing
November 2011

Mutation nomenclature in practice: findings and recommendations from the cystic fibrosis external quality assessment scheme.

Hum Mutat 2011 Nov 17;32(11):1197-203. Epub 2011 Aug 17.

Center for Human Genetics, Biomedical Quality Assurance Research Unit, Katholieke Universiteit Leuven, Belgium.

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http://sefq.es/CFnomenclature2011.pdf
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http://doi.wiley.com/10.1002/humu.21569
Publisher Site
http://dx.doi.org/10.1002/humu.21569DOI Listing
November 2011

Clinical utility gene card for: Haemochromatosis [HFE].

Eur J Hum Genet 2010 Sep 3;18(9). Epub 2010 Feb 3.

Institute of Human Genetics, Medical School Hannover, Hannover, Germany.

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http://dx.doi.org/10.1038/ejhg.2009.245DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987432PMC
September 2010

Digenic mutations in severe congenital neutropenia.

Haematologica 2010 Jul 10;95(7):1207-10. Epub 2010 Mar 10.

Department of Pediatric Hematology and Oncology/Molecular Hematopoiesis, Medizinische Hochschule Hannover, Carl-Neuberg-Str. 1, D-30625 Hannover, Germany.

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http://dx.doi.org/10.3324/haematol.2009.017665DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2895047PMC
July 2010

No association between CALCA polymorphisms and clinical outcome or serum procalcitonin levels in German polytrauma patients.

Cytokine 2009 Jul 15;47(1):30-6. Epub 2009 May 15.

Trauma Department, Medical School Hannover, Carl Neuberg Strasse 1, 30625 Hannover, Germany.

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http://dx.doi.org/10.1016/j.cyto.2009.04.002DOI Listing
July 2009

A novel approach to CFTR mutation testing by pyrosequencing-based assay panels adapted to ethnicities.

Clin Chem 2009 Jun 16;55(6):1083-91. Epub 2009 Apr 16.

Department of Clinical Chemistry and Laboratory Medicine, Johannes Gutenberg University Mainz, Mainz, Germany.

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http://dx.doi.org/10.1373/clinchem.2008.120220DOI Listing
June 2009

No association of CNR1 gene variations with susceptibility to schizophrenia.

Neurosci Lett 2007 Oct 10;426(1):29-33. Epub 2007 Aug 10.

Department of Clinical Psychiatry and Psychotherapy, Medical School Hannover, Hannover, Germany.

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http://dx.doi.org/10.1016/j.neulet.2007.08.008DOI Listing
October 2007

Association of IL-8-251A/T polymorphism with incidence of Acute Respiratory Distress Syndrome (ARDS) and IL-8 synthesis after multiple trauma.

Cytokine 2007 Mar 10;37(3):192-9. Epub 2007 May 10.

Trauma Department, Medical School Hannover, Carl-Neuberg Strasse 1, 30625 Hannover, Germany.

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http://dx.doi.org/10.1016/j.cyto.2007.03.008DOI Listing
March 2007

Hereditary hemorrhagic telangiectasia. Genetics, pathogenesis, clinical manifestation and management.

Saudi Med J 2007 Jan;28(1):11-21

Institute of Human Genetics, Carl-Neuberg-Strasse 1, Medical University of Hannover, D-30625 Hannover, Federal Republic of Germany.

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January 2007

Genetic predisposition for a compromised immune system after multiple trauma.

Shock 2005 Dec;24(6):518-22

Trauma Department and Department of Human Genetics, Medical School Hannover, Carl-Neuberg Strasse 1, 30625 Hannover, Germany.

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http://dx.doi.org/10.1097/01.shk.0000184212.97488.4eDOI Listing
December 2005

Genotype-based screening for hereditary haemochromatosis. I: Technical performance, costs and clinical relevance of a German pilot study.

Eur J Hum Genet 2005 Jan;13(1):69-78

Institute of Human Genetics, Hannover Medical School, Hannover, Germany.

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http://dx.doi.org/10.1038/sj.ejhg.5201287DOI Listing
January 2005

Naxos disease in an Arab family is not caused by the Pk2157del2 mutation. Evidence for exclusion of the plakoglobin gene.

Saudi Med J 2004 Oct;25(10):1449-52

Institute of Human Genetics, Medical University Hannover, Hannover, Federal Republic of Germany.

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October 2004

Mutation at the SCA17 locus is not a common cause of primary dystonia.

J Neurol 2004 Oct;251(10):1232-4

Department of Medical Genetics, University Tübingen, Calwerstrasse 7, 72076 Tübingen, Germany.

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http://dx.doi.org/10.1007/s00415-004-0520-2DOI Listing
October 2004

Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene.

Am J Med Genet B Neuropsychiatr Genet 2004 May;127B(1):97-103

Institute of Human Genetics, Hannover Medical School, Hannover, Germany.

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http://dx.doi.org/10.1002/ajmg.b.20159DOI Listing
May 2004

CFTR gene mutations in sarcoidosis.

Eur J Hum Genet 2002 Nov;10(11):729-32

Institute of Human Genetics, Medical University Lübeck, Lübeck, Germany.

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http://dx.doi.org/10.1038/sj.ejhg.5200868DOI Listing
November 2002

PCR-based analysis of cystic fibrosis mutations specific for Saudi patients.

Saudi Med J 1998 Mar;19(2):148-152

Institute of Human Genetics, Medical School of Hannover, Hannover, Germany.

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March 1998