A Hackett - AI Profile | 人才画像

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论文共 11 篇作者统计合作学者相似作者

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X-exome Sequencing of 405 Unresolved Families Identifies Seven Novel Intellectual Disability Genes

H Hu,S A Haas,J Chelly,H Van Esch,M Raynaud,A P M de Brouwer,S Weinert,G Froyen,S G M Frints,F Laumonnier,T Zemojtel,M I Love,H Richard,A-K Emde,M Bienek,C Jensen,M Hambrock,U Fischer, C Langnick, M Feldkamp, W Wissink-Lindhout,N Lebrun,L Castelnau, J Rucci,R Montjean,O Dorseuil,P Billuart, T Stuhlmann,M Shaw,M A Corbett,A Gardner,S Willis-Owen,C Tan,K L Friend, S Belet,K E P van Roozendaal, M Jimenez-Pocquet,M-P Moizard,N Ronce,R Sun,S O'Keeffe, R Chenna,A van Bömmel,J Göke,A Hackett,M Field, L Christie,J Boyle,E Haan,J Nelson,G Turner,G Baynam,G Gillessen-Kaesbach,U Müller,D Steinberger,B Budny,M Badura-Stronka,A Latos-Bieleńska,L B Ousager,P Wieacker,G Rodríguez Criado,M-L Bondeson, G Annerén,A Dufke,M Cohen,L Van Maldergem,C Vincent-Delorme, B Echenne,B Simon-Bouy,T Kleefstra,M Willemsen,J-P Fryns,K Devriendt,R Ullmann,M Vingron,K Wrogemann,T F Wienker,A Tzschach,H van Bokhoven,J Gecz,T J Jentsch,W Chen,H-H Ropers,V M Kalscheuer

Molecular psychiatry（2015）

引用263浏览0WOSNATURE引用

263

Preliminary Evidence of an Effect of Cerebellar Volume on Postural Sway in FMR1 Premutation Males

R. C. Birch,D. R. Hocking,K. M. Cornish,J. C. Menant,N. Georgiou-Karistianis,D. E. Godler,W. Wen,A. Hackett,C. Rogers,J. N. Trollor

Genes Brain & Behavior（2015）

引用22浏览0WOS引用

Next‐generation sequencing in >450 families with X‐linked intellectual disability

user-5e8423bd4c775ee160ac3e1a（2013）

引用1浏览0引用

Screening and Cell-Based Assessment of Mutations in the Aristaless-Related Homeobox (arx) Gene

T. Fullston,M. Finnis,A. Hackett,B. Hodgson,L. Brueton,G. Baynam,A. Norman,O. Reish,C. Shoubridge,J. Gecz

Clinical genetics（2011）

引用25浏览0WOS引用

Massively parallel sequencing in >250 families with X linked intellectual disability

VM Kalscheuer,H Hu, SA Haas,J Chelly,Hilde Van Esch, M Rayknaud,A De Brouwer, T Zemotjel,S Weinert,Guy Froyen, Sgm Frynts,F Laumonnier, MI Love,H Richard,AK Emde,M Bienek,C Jensen,M Hambrock, C Langnick, M Feldkamp, W Wissink-Lindhout,N Lebrun,L Castelnau,M Shaw,MA Corbett,A Gardner,S Willis-Owen,C Tan, KL Friend, S Belet, Kep Van Roozendaal, M Jimenez-Pocquet,MP Moizard,N Ronce,R Sun, S O'Keeffef, R Chenna, A Mysickova,J Göke,A Hackett,M Field,E Haan,J Nelson,G Turner,G Baynam,G Gillessen-Kaesbach,U Müller,D Steinberger,B Budny,M Badura-Stronka,A Latos-Bielenska, LB Ousager,P Wieacker, GR Criado,ML Bondeson,A Dufke,M Cohen,L Van Maldergem, C Cincent-delorme, B Echenne,B Simon-Bouy,T Kleefstra,M Willemsen,Jean-Pierre Fryns,Koenraad Devriendt,M Vingron,K Wrogemann,R Ullmann,J Gecz,A Tzschach,H Van Bokhoven, J Jentsch,W Chen,HH Ropers

user-5e8423bd4c775ee160ac3e1a（2011）

引用1浏览0引用

Fine-scale Survey of X Chromosome Copy Number Variants Underlying Intellectual Disability

Lucy Raymond,A. C. Whibley,V. Plagnol,P. S. Tarpey,F. Abidi,T. Fullston,L. Willatt,M. Shaw,R. E. Stevenson,G. Turner,M. Field,A. Hackett,C. E. Schwartz,J. Gecz,M. R. Stratton

The American Journal of Human Genetics（2010）

引用112浏览0EIWOS引用

112

Clinical and Molecular Delineation of the 17q21.31 Microdeletion Syndrome

D. A. Koolen,A. J. Sharp,J. A. Hurst,H. V. Firth,S. J. L. Knight,A. Goldenberg,P. Saugier-Veber,R. Pfundt,L. E. L. M. Vissers,A. Destree,B. Grisart,L. Rooms,N. Van der Aa,M. Field,A. Hackett,K. Bell,M. J. M. Nowaczyk,G. M. S. Mancini,P. J. Poddighe,C. E. Schwartz,E. Rossi,M. De Gregori, L. L. Antonacci-Fulton,M. D. McLellan, J. M. Garrett, M. A. Wiechert, T. L. Miner,S. Crosby,R. Ciccone,L. Willatt,A. Rauch,M. Zenker,S. Aradhya, M. A. Manning,T. M. Strom, J. Wagenstaller, A. C. Krepischi-Santos,A. M. Vianna-Morgante,C. Rosenberg,S. M. Price,H. Stewart,C. Shaw-Smith,H. G. Brunner,A. O. M. Wilkie,J. A. Veltman,O. Zuffardi,E. E. Eichler,B. B. A. de Vries

Journal of medical genetics（2008）

引用196浏览0WOS引用

196

Significant association of haplotype blocks in the urokinase type plasminogen activator gene on chromosome 10 with A beta 42 and late onset Alzheimer's disease

N Ertekin-Taner,M Tucker,J Ronald,S Younkin,L Younkin,M Hella,S Jain,D Fadale,A Hackett, L Scanlin, J Kelly, M Kihiko-Ehman,S Edland, W Markesberry,R Petersen,N Graff-Radford,M Hutton,S Estus,SG Younkin

AMERICAN JOURNAL OF HUMAN GENETICS（2002）

引用0浏览0引用

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