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Van Bokhoven H
Van Bokhoven H
Biology
Genetics
X chromosome
Gene
Paresis
4
Papers
2
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0
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Human neuronal networks on micro-electrode arrays are a highly robust tool to study disease-specific genotype-phenotype correlations in vitro
2021
bioRxiv
Mossink B
Anouk H.A. Verboven
van Hugte E
Teun Klein Gunnewiek
Parodi G
Katrin Linda
Chantal Schoenmaker
Tjitske Kleefstra
Tamas Kozicz
Van Bokhoven H
Dirk Schubert
Nael Nadif Kasri
Monica Frega
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Loss-of-function variants in the schizophrenia risk gene SETD1A alter neuronal network activity in human neurons through cAMP/PKA pathway
2021
bioRxiv
Shan Wang
van der Geest, , R.J.
Ibrahim A. Akkouh
Kogo N
Maas N
Bleeck A
Lewerissa E
Wu Km
Chantal Schoenmaker
Srdjan Djurovic
Van Bokhoven H
Tjitske Kleefstra
Nael Nadif Kasri
Dirk Schubert
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Rare genetic variants in MEPE cause congenital facial paresis with stapes fixation, and are associated with otosclerosis
2018
H Valgaeren
I Schrauwen
L. Tomas-Roca
U. Altunoglu
M Wesdorp
Manou Sommen
M. Rahmouni
van Beusekom, , E.
M. J. Huentelman
E.E. Offeciers
I. Dhooghe
R Vincent
A. Huber
Van de Heyning P
D. Zanetti
de Leenheer, , E.M.R.
C. Gilissen
Cor Cremers
B. Verbist
de Brouwer, , A.P.M.
G W Padberg
H. Kremer
Van Camp G
Van Bokhoven H
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Identification and characterization of new mental retardation genes linked to the X chromosome
2005
Aline Dubos
Olivier Hagens
Abvidi F
Claude Moraine
Fryns Jean-Pierre
Jamel Chelly
Van Bokhoven H
Jozef Gecz
Hans-Hilger Ropers
Charles E. Schwartz
De Cassia Stocco Dos Santos R
Kalscheuer
André Hanauer
Jla
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