Jean-Baptiste Cazier


Ontology type: schema:Person     


Person Info

NAME

Jean-Baptiste

SURNAME

Cazier

Publications in SciGraph latest 50 shown

  • 2021-06-14 Identification of maternal continuous glucose monitoring metrics related to newborn birth weight in pregnant women with gestational diabetes in ENDOCRINE
  • 2020-12-10 Severity of COVID-19 in children with cancer: Report from the United Kingdom Paediatric Coronavirus Cancer Monitoring Project in BRITISH JOURNAL OF CANCER
  • 2019-06-04 Robust hematopoietic specification requires the ubiquitous Sp1 and Sp3 transcription factors in EPIGENETICS & CHROMATIN
  • 2019-03-06 Systems Genetics of Hepatic Metabolome Reveals Octopamine as a Target for Non-Alcoholic Fatty Liver Disease Treatment in SCIENTIFIC REPORTS
  • 2018-05-08 Translational study identifies XPF and MUS81 as predictive biomarkers for oxaliplatin-based peri-operative chemotherapy in patients with esophageal adenocarcinoma in SCIENTIFIC REPORTS
  • 2017-11-01 NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease in MUCOSAL IMMUNOLOGY
  • 2016-09-30 Topological analysis of metabolic networks integrating co-segregating transcriptomes and metabolomes in type 2 diabetic rat congenic series in GENOME MEDICINE
  • 2016-04-05 Differential clonal evolution in oesophageal cancers in response to neo-adjuvant chemotherapy in NATURE COMMUNICATIONS
  • 2015-05-18 Factors influencing success of clinical genome sequencing across a broad spectrum of disorders in NATURE GENETICS
  • 2014-05-01 Circulating lipid levels and risk of coronary artery disease in a large group of patients undergoing coronary angiography in JOURNAL OF THROMBOSIS AND THROMBOLYSIS
  • 2014-04-29 Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden in NATURE COMMUNICATIONS
  • 2014-03-31 Choice of transcripts and software has a large effect on variant annotation in GENOME MEDICINE
  • 2013-11-12 A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer in HUMAN GENETICS
  • 2013-07-25 Technical and implementation issues in using next-generation sequencing of cancers in clinical practice in BRITISH JOURNAL OF CANCER
  • 2013-01-26 A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12 in BMC GENOMICS
  • 2013-01-03 Analysis of colorectal cancers in British Bangladeshi identifies early onset, frequent mucinous histotype and a high prevalence of RBFOX1 deletion in MOLECULAR CANCER
  • 2012-12-23 Germline mutations in the proof-reading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas in NATURE GENETICS
  • 2012-12-02 Large-scale association analysis identifies new risk loci for coronary artery disease in NATURE GENETICS
  • 2012-09-09 Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett’s esophagus in NATURE GENETICS
  • 2012-05-02 CNVs leading to fusion transcripts in individuals with autism spectrum disorder in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2012-02-07 Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration in THE PHARMACOGENOMICS JOURNAL
  • 2012-01-19 Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemia in LEUKEMIA
  • 2011-01-19 Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2010-10-24 Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33 in NATURE GENETICS
  • 2010-03-16 High-resolution genomic profiling of human papillomavirus-associated vulval neoplasia in BRITISH JOURNAL OF CANCER
  • 2008-07-16 Deciphering the genetics of hereditary non-syndromic colorectal cancer in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2008-03-30 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3 in NATURE GENETICS
  • 2007-12-16 Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk in NATURE GENETICS
  • 2007-10-14 A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk in NATURE GENETICS
  • 2007-07-08 A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21 in NATURE GENETICS
  • 2006-05-07 A common variant associated with prostate cancer in European and African populations in NATURE GENETICS
  • 2005-01-16 A common inversion under selection in Europeans in NATURE GENETICS
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