Frank Kooy

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Rudi D'HoogeFull professor, Biological Psychology, KU Leuven; visiting professor, VU BrusselsE-mail confirmado em kuleuven.be
Charlotte D'HulstOlfactory Neuroscientist / Biotechnology EntrepreneurE-mail confirmado em genectr.hunter.cuny.edu
Debby Van DamAssociated Professor at the University of Antwerp; Belgium and UMCG, The NetherlandsE-mail confirmado em uantwerpen.be
Céline HelsmoortelDepartment of Medical Genetics, University of Antwerp, Antwerp, BelgiumE-mail confirmado em uantwerpen.be
Lisenka VissersProfessor of Translational Genomics 🧬E-mail confirmado em radboudumc.nl
Illana GozesProfessor Emerita, Former Lily & Avraham Gildor Chair, Head, Elton Lab. Molecular NeuroendocrinologyE-mail confirmado em tauex.tau.ac.il
Flora TassoneProfessorE-mail confirmado em ucdavis.edu
Charles SchwartzDirector of Research, Greenwood Genetic CenterE-mail confirmado em ggc.org
David KoolenRadboudumcE-mail confirmado em radboudumc.nl
Corrado RomanoAssociate Professor of Medical Genetics, University of CataniaE-mail confirmado em oasi.en.it
Patrick CrasUniversity of AntwerpE-mail confirmado em uza.be
Erik SistermansHead of Genome Diagnostics, Amsterdam University Medical CentersE-mail confirmado em amsterdamumc.nl
David R FitzPatrickProfessor & Consultant in Paediatric Genetics, MRC Human Genetics Unit, University of EdinburghE-mail confirmado em nhs.net
Annemie Van der LindenUniversity of AntwerpE-mail confirmado em uantwerpen.be
jean louis mandelprof. Collège de france (chaire génétique humaine), responsable labo. diagnostic génét. CHUE-mail confirmado em igbmc.fr
geert mortierUniversiteit AntwerpenE-mail confirmado em telenet.be
Jozef GeczThe University of AdelaideE-mail confirmado em adelaide.edu.au
Marleen VerhoyeBio-Imaging Lab, University of AntwerpE-mail confirmado em uantwerpen.be
Guy NagelsProfessor of Digital Medicine, Vrije Universiteit BrusselE-mail confirmado em vub.be
William Ted BrownInstitute for Basic ResearchE-mail confirmado em sydney.edu.au

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Frank Kooy

Professor in Cognitive Genetics

E-mail confirmado em uantwerpen.be - Página inicial

Genetics of Intellectual disabitilty autism and related cognitive disorders


Título Ordenar por citações Ordenar por ano Ordenar por título	Citado por Citado por	Ano
The Collaborative Cross, a community resource for the genetic analysis of complex traits Nature genetics 36 (11), 1133-1137, 2004	1216	2004
Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile‐X syndrome: a quantitative examination SA Irwin, B Patel, M Idupulapati, JB Harris, RA Crisostomo, BP Larsen, ... American journal of medical genetics 98 (2), 161-167, 2001	927	2001
Fragile X syndrome RJ Hagerman, E Berry-Kravis, HC Hazlett, DB Bailey, H Moine, RF Kooy, ... Nature reviews Disease primers 3 (1), 1-19, 2017	791	2017
A new highly penetrant form of obesity due to deletions on chromosome 16p11. 2 RG Walters, S Jacquemont, A Valsesia, AJ De Smith, D Martinet, ... Nature 463 (7281), 671-675, 2010	632	2010
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases HAF Stessman, BO Xiong, BP Coe, T Wang, K Hoekzema, M Fenckova, ... Nature genetics 49 (4), 515-526, 2017	580	2017
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11. 2 locus S Jacquemont, A Reymond, F Zufferey, L Harewood, RG Walters, ... Nature 478 (7367), 97-102, 2011	559	2011
A new chromosome 17q21. 31 microdeletion syndrome associated with a common inversion polymorphism DA Koolen, LELM Vissers, R Pfundt, N De Leeuw, SJL Knight, R Regan, ... Nature genetics 38 (9), 999-1001, 2006	524	2006
Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles SL Nolin, WT Brown, A Glicksman, GE Houck Jr, AD Gargano, A Sullivan, ... The American Journal of Human Genetics 72 (2), 454-464, 2003	473	2003
A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP C Helsmoortel, AT Vulto-van Silfhout, BP Coe, G Vandeweyer, L Rooms, ... Nature genetics 46 (4), 380-384, 2014	378	2014
Decreased expression of the GABAA receptor in fragile X syndrome C d'Hulst, N De Geest, SP Reeve, D Van Dam, PP De Deyn, BA Hassan, ... Brain research 1121 (1), 238-245, 2006	369	2006
A 600 kb deletion syndrome at 16p11. 2 leads to energy imbalance and neuropsychiatric disorders F Zufferey, EH Sherr, ND Beckmann, E Hanson, AM Maillard, L Hippolyte, ... Journal of medical genetics 49 (10), 660-668, 2012	331	2012
The GABAA receptor as a therapeutic target for neurodevelopmental disorders S Braat, RF Kooy Neuron 86 (5), 1119-1130, 2015	328	2015
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome BWM Van Bon, HC Mefford, B Menten, DA Koolen, AJ Sharp, ... Journal of medical genetics 46 (8), 511-523, 2009	319	2009
Mutations in DDX3X are a common cause of unexplained intellectual disability with gender-specific effects on Wnt signaling LS Blok, E Madsen, J Juusola, C Gilissen, D Baralle, MRF Reijnders, ... The American Journal of Human Genetics 97 (2), 343-352, 2015	307	2015
L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patterns E Fransen, R d'Hooge, G Van Camp, M Verhoye, J Sijbers, E Reyniers, ... Human molecular genetics 7 (6), 999-1009, 1998	295	1998
Mildly impaired water maze performance in maleFmr1 knockout mice R D'Hooge, G Nagels, F Franck, CE Bakker, E Reyniers, K Storm, ... Neuroscience 76 (2), 367-376, 1997	252	1997
Transgenic mouse model for the fragile X syndrome RF Kooy, R D'Hooge, E Reyniers, CE Bakker, G Nagels, K De Boulle, ... American journal of medical genetics 64 (2), 241-245, 1996	239	1996
The complexity of the GABAA receptor shapes unique pharmacological profiles C D’Hulst, JR Atack, RF Kooy Drug discovery today 14 (17-18), 866-875, 2009	231	2009
Fourteen new cases contribute to the characterization of the 7q11. 23 microduplication syndrome N Van der Aa, L Rooms, G Vandeweyer, J van den Ende, E Reyniers, ... European journal of medical genetics 52 (2-3), 94-100, 2009	228	2009
Long‐term potentiation in the hippocampus of fragile X knockout mice JM Godfraind, E Reyniers, K De Boulle, R D'hooge, PP De Deyn, ... American journal of medical genetics 64 (2), 246-251, 1996	214	1996

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