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Authors whose works are in public domain in at least one jurisdiction

List of works by Jean-Baptiste Cazier

1-50 of 54 results

Genetic studies of body mass index yield new insights for obesity biology

scientific article

Large-scale association analysis identifies new risk loci for coronary artery disease

scientific article published on 02 December 2012

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21

article

New genetic loci link adipose and insulin biology to body fat distribution

scientific article

Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas

scientific article

A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3

article

Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer

scientific article

A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk

article

Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33

scientific article

Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk

scientific article published on 16 December 2007

Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

scientific article

Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer

scientific article

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain

scientific article

Linkage of osteoporosis to chromosome 20p12 and association to BMP2

scientific article

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

scientific article

A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12

scientific article published on 05 February 2009

Congenital myasthenic syndromes due to mutations in ALG2 and ALG14.

scientific article

Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes

scientific article

Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden

scientific article

Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer

article

Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia

article published in 2008

Technical and implementation issues in using next-generation sequencing of cancers in clinical practice

scientific article published on July 25, 2013

Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor development

scientific article (publication date: 2012)

Recurrent chromosomal gains and heterogeneous driver mutations characterise papillary renal cancer evolution

scientific article

Large scale association analysis identifies three susceptibility loci for coronary artery disease

scientific article (publication date: 2011)

Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemia

scientific article published on January 19, 2012

Differential clonal evolution in oesophageal cancers in response to neo-adjuvant chemotherapy

scientific article published on 5 April 2016

Single nucleotide polymorphism array analysis defines a specific genetic fingerprint for well-differentiated cutaneous SCCs

scientific article published on 8 January 2009

Analysis of colorectal cancers in British Bangladeshi identifies early onset, frequent mucinous histotype and a high prevalence of RBFOX1 deletion

scientific article published on 3 January 2013

A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.

scientific article

Deciphering the genetics of hereditary non-syndromic colorectal cancer

scientific article published on 16 July 2008

Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis

scientific article

Nutrigenomics of high fat diet induced obesity in mice suggests relationships between susceptibility to fatty liver disease and the proteasome

scientific article

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population

scientific article

Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13

scientific article published on 10 November 2011

CNVs leading to fusion transcripts in individuals with autism spectrum disorder

scientific article (publication date: November 2012)

Germline deletions in the tumour suppressor gene FOCAD are associated with polyposis and colorectal cancer development.

scientific article published on 26 March 2015

Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment

scientific article

mQTL.NMR: an integrated suite for genetic mapping of quantitative variations of (1)H NMR-based metabolic profiles

scientific article published on 2 April 2015

SNP rs6457327 in the HLA region on chromosome 6p is predictive of the transformation of follicular lymphoma

scientific article

Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment

scientific article

Broad-Ranging Natural Metabotype Variation Drives Physiological Plasticity in Healthy Control Inbred Rat Strains

scientific article published on 15 March 2011

Multiple Segmental Uniparental Disomy Associated with Abnormal DNA Methylation of Imprinted Loci in Silver-Russell Syndrome

scientific article published on August 31, 2012

Identification of genomic changes associated with cisplatin resistance in testicular germ cell tumor cell lines

scientific article published on 01 July 2008

GREVE: Genomic Recurrent Event ViEwer to assist the identification of patterns across individual cancer samples

scientific article published on September 8, 2012

Topological analysis of metabolic networks integrating co-segregating transcriptomes and metabolomes in type 2 diabetic rat congenic series

scientific article published on 30 September 2016

High-resolution genomic profiling of human papillomavirus-associated vulval neoplasia

scientific article

Development and Validation of a Combined Hypoxia and Immune Prognostic Classifier for Head and Neck Cancer

scientific article published on 10 June 2019

A novel test for gene-ancestry interactions in genome-wide association data

scientific article

Novel putative drugs and key initiating genes for neurodegenerative disease determined using network-based genetic integrative analysis

article