Detalles de la búsqueda
1.
GWAS meta-analysis of 16 790 patients with Barrett's oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology beyond the single marker level.
Gut
; 72(4): 612-623, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35882562
2.
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis.
Gut
; 71(6): 1053-1061, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-34187846
3.
Germline variation in the insulin-like growth factor pathway and risk of Barrett's esophagus and esophageal adenocarcinoma.
Carcinogenesis
; 42(3): 369-377, 2021 04 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-33300568
4.
Sex-Specific Genetic Associations for Barrett's Esophagus and Esophageal Adenocarcinoma.
Gastroenterology
; 159(6): 2065-2076.e1, 2020 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-32918910
5.
[Support for innovation at the BfArM-experiences from the consultations on digital health applications (DiGA)]. / Innovationsunterstützung im BfArM Erfahrungen aus den Beratungen zu digitalen Gesundheitsanwendungen (DiGA).
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz
; 64(10): 1241-1248, 2021 Oct.
Artículo
en Alemán
| MEDLINE | ID: mdl-34519834
6.
Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.
Hum Mol Genet
; 26(4): 829-842, 2017 02 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-28087736
7.
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.
Am J Hum Genet
; 98(4): 755-62, 2016 Apr 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-27018475
8.
No Association Between Vitamin D Status and Risk of Barrett's Esophagus or Esophageal Adenocarcinoma: A Mendelian Randomization Study.
Clin Gastroenterol Hepatol
; 17(11): 2227-2235.e1, 2019 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-30716477
9.
Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.
PLoS Genet
; 12(3): e1005914, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26968009
10.
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome.
Am J Hum Genet
; 95(6): 698-707, 2014 Dec 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-25434003
11.
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.
Lancet Oncol
; 17(10): 1363-1373, 2016 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-27527254
12.
Replication analysis of 15 susceptibility loci for nonsyndromic cleft lip with or without cleft palate in an italian population.
Birth Defects Res A Clin Mol Teratol
; 106(2): 81-7, 2016 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-26648166
13.
Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.
Birth Defects Res A Clin Mol Teratol
; 106(9): 767-72, 2016 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-27384521
14.
Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia.
J Psychiatry Neurosci
; 39(6): 386-96, 2014 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-24936775
15.
Nonsyndromic cleft lip with or without cleft palate in arab populations: genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen.
Birth Defects Res A Clin Mol Teratol
; 100(4): 307-13, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-24634360
16.
Evaluating eight newly identified susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population.
Birth Defects Res A Clin Mol Teratol
; 100(1): 43-7, 2014 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24382704
17.
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway.
Birth Defects Res A Clin Mol Teratol
; 100(6): 493-8, 2014 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-24706492
18.
Analysis of susceptibility loci for nonsyndromic orofacial clefting in a European trio sample.
Am J Med Genet A
; 161A(10): 2545-9, 2013 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-24038802
19.
eQTL Set-Based Association Analysis Identifies Novel Susceptibility Loci for Barrett Esophagus and Esophageal Adenocarcinoma.
Cancer Epidemiol Biomarkers Prev
; 31(9): 1735-1745, 2022 09 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-35709760
20.
Strengthening regulatory science in academia: STARS, an EU initiative to bridge the translational gap.
Drug Discov Today
; 26(2): 283-288, 2021 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33127567