F. Hannes

发表

Nuclear speckles and nucleoli targeting by PIP2–PDZ domain interactions

P. Zimmermann, G. David, E. Mortier, 2005, The EMBO journal.

Telomere healing following DNA polymerase arrest‐induced breakages is likely the main mechanism generating chromosome 4p terminal deletions

R. Hochstenbach, M. Poot, J. Vermeesch, 2010, Human mutation.

A microdeletion proximal of the critical deletion region is associated with mild Wolf–Hirschhorn syndrome

K. Devriendt, J. Vermeesch, P. Hammond, 2012, American journal of medical genetics. Part A.

Characterizing the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf-Hirschhorn syndrome.

J. Vermeesch, M. O’Driscoll, C. Kerzendorfer, 2012, Human molecular genetics.

Fine-grained facial phenotype–genotype analysis in Wolf–Hirschhorn syndrome

Peter Hammond, Francesca Forzano, Oliver Quarrell, 2011, European Journal of Human Genetics.

The Molecular Dissection of Contiguous Gene Syndromes with a Focus on 4p16 Deletion Syndrome

F. Hannes, 2011 .

Benign and pathogenic copy number variation on the short arm of chromosome 4

J. Vermeesch, F. Hannes, 2009, Cytogenetic and Genome Research.

Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)

K. Devriendt, J. Vermeesch, K. Kok, 2007, Journal of Medical Genetics.

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant

H. Mefford, E. Eichler, R. Regan, 2008, Journal of Medical Genetics.

Molecular karyotyping of patients with MCA/MR: the blurred boundary between normal and pathogenic variation

T. de Ravel, K. Devriendt, J. Vermeesch, 2006, Cytogenetic and Genome Research.

Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delay.

J. Vermeesch, O. Haus, F. Hannes, 2010, European journal of medical genetics.

Pathogenic significance of deletions distal to the currently described Wolf–Hirschhorn syndrome critical regions on 4p16.3

S. South, J. Vermeesch, G. Fisch, 2008, American journal of medical genetics. Part C, Seminars in medical genetics.

An experimental loop design for the detection of constitutional chromosomal aberrations by array CGH

Bart De Moor, Yves Moreau, Joris Robert Vermeesch, 2009, BMC Bioinformatics.

The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at random.

S. van Vooren, Y. Moreau, K. Devriendt, 2007, Genetic counseling.

Optimizing health and nutrition status of migrant construction workers consuming multiple micronutrient fortified rice in Singapore

F. Hannes, Kevin Moon, Regina Moench Pfanner, 2023, PloS one.

Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)

K. Devriendt, J. Vermeesch, K. Kok, 2007, Journal of Medical Genetics.

A microdeletion proximal of the critical deletion region is associated with mild Wolf–Hirschhorn syndrome

K. Devriendt, J. Vermeesch, P. Hammond, 2012, American journal of medical genetics. Part A.