Frank Kooy

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Rudi D'HoogeFull professor, Biological Psychology, KU Leuven; visiting professor, VU BrusselsEmail verificata su kuleuven.be
Charlotte D'HulstOlfactory Neuroscientist / Biotechnology EntrepreneurEmail verificata su genectr.hunter.cuny.edu
Debby Van DamAssociated Professor at the University of Antwerp; Belgium and UMCG, The NetherlandsEmail verificata su uantwerpen.be
Céline HelsmoortelDepartment of Medical Genetics, University of Antwerp, Antwerp, BelgiumEmail verificata su uantwerpen.be
Lisenka VissersProfessor of Translational Genomics 🧬Email verificata su radboudumc.nl
Illana GozesProfessor Emerita, Former Lily & Avraham Gildor Chair, Head, Elton Lab. Molecular NeuroendocrinologyEmail verificata su tauex.tau.ac.il
Flora TassoneProfessorEmail verificata su ucdavis.edu
Charles SchwartzDirector of Research, Greenwood Genetic CenterEmail verificata su ggc.org
David KoolenRadboudumcEmail verificata su radboudumc.nl
Corrado RomanoAssociate Professor of Medical Genetics, University of CataniaEmail verificata su oasi.en.it
Erik SistermansHead of Genome Diagnostics, Amsterdam University Medical CentersEmail verificata su amsterdamumc.nl
Patrick CrasUniversity of AntwerpEmail verificata su uza.be
Annemie Van der LindenUniversity of AntwerpEmail verificata su uantwerpen.be
David R FitzPatrickProfessor & Consultant in Paediatric Genetics, MRC Human Genetics Unit, University of EdinburghEmail verificata su nhs.net
jean louis mandelprof. Collège de france (chaire génétique humaine), responsable labo. diagnostic génét. CHUEmail verificata su igbmc.fr
geert mortierUniversiteit AntwerpenEmail verificata su telenet.be
Jozef GeczThe University of AdelaideEmail verificata su adelaide.edu.au
Marleen VerhoyeBio-Imaging Lab, University of AntwerpEmail verificata su uantwerpen.be
Guy NagelsProfessor of Digital Medicine, Vrije Universiteit BrusselEmail verificata su vub.be
William Ted BrownInstitute for Basic ResearchEmail verificata su sydney.edu.au

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Frank Kooy

Professor in Cognitive Genetics

Email verificata su uantwerpen.be - Home page

Genetics of Intellectual disabitilty autism and related cognitive disorders


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
The Collaborative Cross, a community resource for the genetic analysis of complex traits Nature genetics 36 (11), 1133-1137, 2004	1218	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	912	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	800	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	626	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	574	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	555	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	531	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	366	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	330	2012
The GABAA receptor as a therapeutic target for neurodevelopmental disorders S Braat, RF Kooy Neuron 86 (5), 1119-1130, 2015	329	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	318	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	303	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	297	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	250	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	237	1996
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	232	2009
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
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	212	1996

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