List of works - Guillaume Smits

The H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1r

scientific article

NOVOPlasty: de novo assembly of organelle genomes from whole genome data

scientific article

Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians

scientific article

Ovarian hyperstimulation syndrome due to a mutation in the follicle-stimulating hormone receptor.

scientific article published in August 2003

Glycoprotein hormone receptors: determinants in leucine-rich repeats responsible for ligand specificity

scientific article

Premature ovarian aging in mice deficient for Gpr3.

scientific article

Presence and absence of follicle-stimulating hormone receptor mutations provide some insights into spontaneous ovarian hyperstimulation syndrome physiopathology.

scientific article

A mutation in the follicle-stimulating hormone receptor as a cause of familial spontaneous ovarian hyperstimulation syndrome.

scientific article published on March 2004

DIDA: A curated and annotated digenic diseases database.

scientific article

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

scientific article published on 28 June 2013

High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.

scientific article

Modulation of ligand selectivity associated with activation of the transmembrane region of the human follitropin receptor.

scientific article published on 27 May 2004

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

scientific article published on 15 February 2014

The specificity of binding of glycoprotein hormones to their receptors

scientific article published on August 2008

Non-coding transcripts in the H19 imprinting control region mediate gene silencing in transgenic Drosophila

scientific article published on 19 October 2007

Understanding ovarian hyperstimulation syndrome

scientific article

LRRC8 extracellular domain is composed of 17 leucine-rich repeats.

scientific article published in July 2004

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

scientific article published on 12 September 2018

HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond

scientific article published on 01 November 2018

Genetic predictors of ovarian hyperstimulation syndrome in women undergoing in vitro fertilization

scientific article published on 01 November 2006

BCL11A frameshift mutation associated with dyspraxia and hypotonia affecting the fine, gross, oral, and speech motor systems

scientific article

Imprinting weaves its web.

scientific article published in November 2006

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

scientific article published on 01 August 2019

List of works by Guillaume Smits

The H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1r

NOVOPlasty: de novo assembly of organelle genomes from whole genome data

Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians

Ovarian hyperstimulation syndrome due to a mutation in the follicle-stimulating hormone receptor.

Glycoprotein hormone receptors: determinants in leucine-rich repeats responsible for ligand specificity

Premature ovarian aging in mice deficient for Gpr3.

Presence and absence of follicle-stimulating hormone receptor mutations provide some insights into spontaneous ovarian hyperstimulation syndrome physiopathology.

A mutation in the follicle-stimulating hormone receptor as a cause of familial spontaneous ovarian hyperstimulation syndrome.

DIDA: A curated and annotated digenic diseases database.

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.

Modulation of ligand selectivity associated with activation of the transmembrane region of the human follitropin receptor.

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

The specificity of binding of glycoprotein hormones to their receptors

Non-coding transcripts in the H19 imprinting control region mediate gene silencing in transgenic Drosophila

Understanding ovarian hyperstimulation syndrome

LRRC8 extracellular domain is composed of 17 leucine-rich repeats.

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond

Genetic predictors of ovarian hyperstimulation syndrome in women undergoing in vitro fertilization

BCL11A frameshift mutation associated with dyspraxia and hypotonia affecting the fine, gross, oral, and speech motor systems

Imprinting weaves its web.

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients