B. Grisart

发表

L. Morando, D. Kahila, A. Vénisse, 2011, Pediatric Nephrology.

Deletion of KDM6A, a histone demethylase interacting with MLL2, in three patients with Kabuki syndrome.

M. Digilio, B. Grisart, B. Dallapiccola, 2012, American journal of human genetics.

Cinematographic analysis of bovine embryo development in serum-free oviduct-conditioned medium.

B. Grisart, F. Dessy, A. Massip, 1994, Journal of reproduction and fertility.

Simultaneous mining of linkage and linkage disequilibrium to fine map quantitative trait loci in outbred half-sib pedigrees: revisiting the location of a quantitative trait locus with major effect on milk production on bovine chromosome 14.

M. Mni, M. Georges, B. Grisart, 2002, Genetics.

Intron 22 homologous regions are implicated in exons 1–22 duplications of the F8 gene

M. Vikkula, B. Grisart, C. Hermans, 2013, European Journal of Human Genetics.

Outcome of publicly funded nationwide first-tier noninvasive prenatal screening

K. Devriendt, B. Menten, J. Vermeesch, 2021, Genetics in Medicine.

Three year results of in vitro production of bovine embryos in serum-poor bovine oviduct conditioned medium. An overview.

B. Grisart, G. Brem, P. Mermillod, 1996, Reproduction, nutrition, development.

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.

T. de Ravel, K. Devriendt, B. Menten, 2014, European journal of medical genetics.

Identification of an NPHP1 deletion causing adult form of nephronophthisis

K. Dahan, B. Grisart, V. Benoit, 2016, Irish Journal of Medical Science (1971 -).

Spectrum of mutations in Gitelman syndrome.

D. Kahila, A. Vénisse, K. Dahan, 2011, Journal of the American Society of Nephrology : JASN.

Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A

M. Vikkula, B. Grisart, C. Hermans, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

Glucose metabolism during bovine preimplantation development: Analysis of gene expression in single oocytes and embryos

B. Grisart, F. Dessy, A. Massip, 1997, Molecular reproduction and development.

Positional candidate cloning of a QTL in dairy cattle: identification of a missense mutation in the bovine DGAT1 gene with major effect on milk yield and composition.

Michel Georges, Frédéric Farnir, Myriam Mni, 2002, Nature Reviews Genetics.

Molecular dissection of a quantitative trait locus: a phenylalanine-to-tyrosine substitution in the transmembrane domain of the bovine growth hormone receptor is associated with a major effect on milk yield and composition.

Michel Georges, Anne Schmidt-Küntzel, Frédéric Farnir, 2002, Genetics.

From phenotype to genotype : towards positional cloning of QTL in livestock?

M. Georges, B. Grisart, W. Coppieters, 1999 .

Fine-mapping of quantitative trait loci by identity by descent in outbred populations: application to milk production in dairy cattle.

M. Mni, M. Georges, B. Grisart, 1999, Proceedings of the National Academy of Sciences of the United States of America.

From Phenotype to Genotype : Towards Positional Cloning of Quantitative Trait Loci in Livestock ?

B. Grisart, F. Farnir, S. Blott, 1999 .

Genetic and functional confirmation of the causality of the DGAT1 K232A quantitative trait nucleotide in affecting milk yield and composition.

Michel Georges, Frédéric Farnir, Myriam Mni, 2004, Proceedings of the National Academy of Sciences of the United States of America.

17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction

J. Rosenfeld, T. de Ravel, J. Vermeesch, 2009, Journal of Medical Genetics.

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

L. Vissers, B. D. de Vries, E. Eichler, 2008, Journal of Medical Genetics.

Variants modulating the expression of a chromosome domain encompassing PLAG1 influence bovine stature

Tom Druet, Michel Georges, Frédéric Farnir, 2011, Nature Genetics.

Trisomy rescue mechanism: the case of concomitant mosaic trisomy 14 and maternal uniparental disomy 14 in a 15‐year‐old girl

B. Grisart, I. Maystadt, Urielle Ullmann, 2016, Clinical case reports.

POSITIONAL CANDIDATE CLONING OF A QTL IN DAIRY CATTLE: IDENTIFICATION OF A MISSENSE MUTATION IN THE BOVINE AND COMPOSITION

B. Grisart, W. Coppieters, F. Farnir, 2001 .

A QTL with major effect on milk yield and composition maps to bovine Chromosome 14

M. Georges, B. Grisart, J. Arranz, 1998, Mammalian Genome.

A QTL affecting milk yield and composition maps to bovine chromosome 20: a confirmation.

M. Georges, B. Grisart, J. Arranz, 1998, Animal genetics.

The sex ratio of bovine embryos produced in vitro in serum-free oviduct cell-conditioned medium is not altered.

L. Collette, B. Grisart, F. Dessy, 1995, Theriogenology.

Effects of co-culture and embryo number on the in vitro development of bovine embryos.

B. Grisart, F. Dessy, A. van Langendonckt, 1997, Theriogenology.

Extensive genome-wide linkage disequilibrium in cattle.

M. Mni, M. Georges, B. Grisart, 2000, Genome research.

Comparison of the effects of oviductal cell co-culture and oviductal cell-conditioned medium on the development and metabolic activity of cattle embryos.

B. Grisart, K. Betteridge, F. Dessy, 1995, Journal of reproduction and fertility.

Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene.

M. Vikkula, B. Grisart, C. Hermans, 2016, Thrombosis research.

Implementation of non‐invasive prenatal testing by semiconductor sequencing in a genetic laboratory

Tom Sante, Sarah Vergult, Björn Menten, 2016, Prenatal diagnosis.

Novel KDM6A (UTX) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (KS2)

B. Grisart, H. Stewart, G. Mancini, 2015, Clinical genetics.

NF1 microduplication first clinical report: association with mild mental retardation, early onset of baldness and dental enamel hypoplasia?

B. Grisart, A. Destrée, P. Deltenre, 2008, European Journal of Human Genetics.

Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan

Christian Gilissen, Han G. Brunner, Michael F. Buckley, 2012, Nature Genetics.

The great-grand-daughter design: a simple strategy to increase the power of a grand-daughter design for QTL mapping

M. Georges, B. Grisart, J. Arranz, 1999 .

Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1-q25.32: Genotype-phenotype correlations of chromosome 3q25 deletion syndrome.

B. Grisart, A. Destrée, I. Maystadt, 2011, European journal of medical genetics.

Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple Gestations

K. Devriendt, J. Vermeesch, J. Gatot, 2021, Obstetrics and gynecology.