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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

Molecular psychiatry, 2008-02, Vol.13 (2), p.197-207

2008

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A similarity-based method for genome-wide prediction of disease-relevant human genes

Bioinformatics (Oxford, England), 2002-10, Vol.18 Suppl 2 (suppl_2), p.S110-S115

2002

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Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder

Molecular psychiatry, 2009-05, Vol.14 (5), p.487-491

2009

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Chromocolonoscopy detects more adenomas than white light colonoscopy or narrow band imaging colonoscopy in hereditary nonpolyposis colorectal cancer screening

Endoscopy, 2009-04, Vol.41 (4), p.316-322

2009

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Genetische Testung in der Onkologie – contra

Deutsche medizinische Wochenschrift, 2008-10, Vol.133 (41), p.2085-2085

Propping, P

2008

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Genetic analysis in oncology--contra

Deutsche medizinische Wochenschrift (1946), 2008-10, Vol.133 (41), p.2085

Propping, P

2008

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Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder

Molecular psychiatry, 2004-02, Vol.9 (2), p.203-207

2004

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High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome

Journal of medical genetics, 2007-11, Vol.44 (11), p.702-709

2007

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DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation

Neurology, 2007-03, Vol.68 (10), p.743-750

2007

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Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

Molecular psychiatry, 2012-04, Vol.17 (4), p.421-432

2012

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A Potassium Channel Mutation in Neonatal Human Epilepsy

Science (American Association for the Advancement of Science), 1998-01, Vol.279 (5349), p.403-406

1998

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Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder

Human molecular genetics, 1999-04, Vol.8 (4), p.621-624

1999

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Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease

Human molecular genetics, 2008-04, Vol.17 (8), p.1137-1146

2008

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A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome

Journal of medical genetics, 2004-07, Vol.41 (7), p.567-572

2004

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Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome

The Journal of pathology, 2008-01, Vol.214 (1), p.10-16

2008

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Small bowel cancer risk in Lynch syndrome

Gut, 2008-11, Vol.57 (11), p.1629-1630

2008

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Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers

Molecular psychiatry, 1999-05, Vol.4 (3), p.290-296

1999

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Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families

Gut, 2001-04, Vol.48 (4), p.515-521

2001

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S3 guidelines for colorectal carcinoma: results of an evidence-based consensus conference on February 6/7, 2004 and June 8/9, 2007 (for the topics IV, VI and VII)

Zeitschrift fur Gastroenterologie, 2010-01, Vol.48 (1), p.65

2010

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Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis

Journal of medical genetics, 2005-02, Vol.42 (2), p.185-192

2005

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Ileorectal anastomosis is appropriate for a subset of patients with familial adenomatous polyposis

Gastroenterology (New York, N.Y. 1943), 2001-08, Vol.121 (2), p.503-504

2001

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Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder

Molecular psychiatry, 2008-03, Vol.13 (3), p.277-284

2008

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MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?

British journal of dermatology (1951), 2007-01, Vol.156 (1), p.158-162

2007

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Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1)

Molecular psychiatry, 2000-05, Vol.5 (3), p.275-282

2000

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Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families

Molecular psychiatry, 1999, Vol.4 (1), p.76-84

1999

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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

A similarity-based method for genome-wide prediction of disease-relevant human genes

Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder

Chromocolonoscopy detects more adenomas than white light colonoscopy or narrow band imaging colonoscopy in hereditary nonpolyposis colorectal cancer screening

Genetische Testung in der Onkologie – contra

Genetic analysis in oncology--contra

Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder

High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome

DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

A Potassium Channel Mutation in Neonatal Human Epilepsy

Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder

Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease

A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome

Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome

Small bowel cancer risk in Lynch syndrome

Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families

S3 guidelines for colorectal carcinoma: results of an evidence-based consensus conference on February 6/7, 2004 and June 8/9, 2007 (for the topics IV, VI and VII)

Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis

Ileorectal anastomosis is appropriate for a subset of patients with familial adenomatous polyposis

Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder

MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?

Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1)

Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families

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