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1.
Identification of loci associated with schizophrenia by genome-wide association and follow-up.
Nat Genet
; 40(9): 1053-5, 2008 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-18677311
2.
Activating ERBB2/HER2 mutations indicate susceptibility to pan-HER inhibitors in Lynch and Lynch-like colorectal cancer.
Gut
; 65(8): 1296-305, 2016 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-26001389
3.
Embryo screening: update German view of genetic testing.
Nature
; 510(7506): 473, 2014 Jun 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-24965640
4.
Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.
Carcinogenesis
; 35(2): 315-23, 2014 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-24127187
5.
Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: a comprehensive analysis of 3,671 families.
Int J Cancer
; 135(1): 69-77, 2014 Jul 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-24493211
6.
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.
Nat Genet
; 33(4): 527-32, 2003 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-12612585
7.
FHL2 expression in peritumoural fibroblasts correlates with lymphatic metastasis in sporadic but not in HNPCC-associated colon cancer.
Lab Invest
; 91(12): 1695-705, 2011 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-21826055
8.
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
Hum Mol Genet
; 18(14): 2719-27, 2009 Jul 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-19414483
9.
Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21.
Am J Med Genet B Neuropsychiatr Genet
; 156B(1): 36-43, 2011 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-21184582
10.
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.
Carcinogenesis
; 31(9): 1612-9, 2010 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-20610541
11.
Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease.
Hum Mol Genet
; 17(8): 1137-46, 2008 Apr 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-18192679
12.
Expanded extracolonic tumor spectrum in MUTYH-associated polyposis.
Gastroenterology
; 137(6): 1976-85.e1-10, 2009 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-19732775
13.
Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer.
Clin Gastroenterol Hepatol
; 8(2): 174-82, 2010 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-19835992
14.
Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study.
BMC Gastroenterol
; 10: 112, 2010 Sep 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-20920174
15.
A systematic association mapping on chromosome 6q in bipolar affective disorder--evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar affective disorder.
Am J Med Genet B Neuropsychiatr Genet
; 153B(4): 878-84, 2010 Jun 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-19927306
16.
European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset.
Am J Med Genet B Neuropsychiatr Genet
; 153B(8): 1425-33, 2010 Dec 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-20886542
17.
Analysis of rare APC variants at the mRNA level: six pathogenic mutations and literature review.
J Mol Diagn
; 11(2): 131-9, 2009 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-19196998
18.
Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.
Bipolar Disord
; 11(6): 610-20, 2009 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-19689503
19.
Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes.
Am J Med Genet B Neuropsychiatr Genet
; 150B(7): 1013-6, 2009 Oct 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-19105200
20.
Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples.
Am J Med Genet B Neuropsychiatr Genet
; 150B(7): 1017-21, 2009 Oct 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-19330776