Publications by authors named "Marc Hooghe"

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Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophy.
Richard J L F Lemmers, Russell Butterfield, Patrick J van der Vliet, Jan L de Bleecker, Ludo van der Pol, Marc D'Hooghe

Brain· February 2024

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Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with .
Giulia Coarelli, Rebecca Schule, Bart P C van de Warrenburg, Peter De Jonghe, Claire Ewenczyk, Marc D'Hooghe

Neurology· June 2019

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Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1.
Stefanie Brock, Katrien Stouffs, Emmanuel Scalais, Marc D'Hooghe, Kathelijn Keymolen

Eur J Hum Genet· August 2018

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A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy.
Cas Simons, David Dyment, Stephen J Bent, Joanna Crawford, Marc D'Hooghe

Brain· December 2017

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Partisan strength, political trust and generalized trust in the United States: An analysis of the General Social Survey, 1972-2014.
Marc Hooghe, Jennifer Oser

Soc Sci Res· November 2017

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Extending trust to immigrants: Generalized trust, cross-group friendship and anti-immigrant sentiments in 21 European societies.
Meta van der Linden, Marc Hooghe, Thomas de Vroome, Colette Van Laar

PLoS One· September 2017

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The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.
Claire Redin, Harrison Brand, Ryan L Collins, Tammy Kammin, Elyse Mitchell, Marc D'Hooghe

Nat Genet· January 2017

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Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutations.
Chantal Depondt, Simona Donatello, Nicolas Simonis, Myriam Rai, Roxane van Heurck, Marc D'Hooghe

Neurology· May 2014

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Variant ataxia telangiectasia: clinical and molecular findings and evaluation of radiosensitive phenotypes in a patient and relatives.
Kathleen Claes, Julie Depuydt, A Malcolm R Taylor, James I Last, Annelot Baert, Marc D'Hooghe

Neuromolecular Med· September 2013

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X-linked sideroblastic anemia and ataxia: a new family with identification of a fourth ABCB7 gene mutation.
Marc D'Hooghe, Dominik Selleslag, Geert Mortier, Rudy Van Coster, Pieter Vermeersch

Eur J Paediatr Neurol· November 2012

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Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction.
Benedetta Izzi, Inge Francois, Veerle Labarque, Chantal Thys, Christine Wittevrongel, Marc D'Hooghe

PLoS One· October 2012

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Homophobia and the transition to adulthood: a three year panel study among Belgian late adolescents and young adults, 2008-2011.
Marc Hooghe, Cecil Meeusen

J Youth Adolesc· September 2012

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Is sexual well-being part of subjective well-being? An empirical analysis of Belgian (Flemish) survey data using an extended well-being scale.
Marc Hooghe

J Sex Res· July 2012

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Characteristics of early MRI in children and adolescents with vanishing white matter.
Hannemieke D van der Lei, Marjan E Steenweg, Frederik Barkhof, Ton de Grauw, Marc d'Hooghe

Neuropediatrics· February 2012

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The impact of gendered friendship patterns on the prevalence of homophobia among belgian late adolescents.
Marc Hooghe

Arch Sex Behav· June 2011

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Anti-gay sentiment among adolescents in Belgium and Canada: a comparative investigation into the role of gender and religion.
Marc Hooghe, Ellen Claes, Allison Harell, Ellen Quintelier, Yves Dejaeghere

J Homosex· September 2010

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Treatment and long term outcome in West syndrome: the clinical reality. A multicentre follow up study.
Lieven Lagae, Helène Verhelst, Berten Ceulemans, Linda De Meirleir, Marie-Cécile Nassogne, Marc D'Hooghe

Seizure· April 2010

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Brief report: Citizenship concepts among adolescents. Evidence from a survey among Belgian 16-year olds.
Yves Dejaeghere, Marc Hooghe

J Adolesc· June 2009

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CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.
Francesco Brancati, Giuseppe Barrano, Jennifer L Silhavy, Sarah E Marsh, Lorena Travaglini, Marc D'Hooghe

Am J Hum Genet· July 2007

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Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy.
Albena Jordanova, Joy Irobi, Florian P Thomas, Patrick Van Dijck, Kris Meerschaert, Marc D'Hooghe

Nat Genet· February 2006

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Steroids in intractable childhood epilepsy: clinical experience and review of the literature.
Helene Verhelst, Paul Boon, Gunnar Buyse, Berten Ceulemans, Marc D'Hooghe

Seizure· September 2005

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Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease.
Rong Li, Anne B Johnson, Gajja Salomons, James E Goldman, Sakkubai Naidu, Marc D'Hooghe

Ann Neurol· March 2005

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