Researcher
Carolien Gf de Kovel
Max-Planck-Institut für Psycholinguistik
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47 papers found
All papers authored by Carolien Gf de Kovel
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Clyde Francks
The molecular genetics of hand preference revisited
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,
Steven N. Lisgo,
Clyde Francks
Transcriptomic analysis of left-right differences in human embryonic forebrain and midbrain
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,
Amaia Carrion-Castillo ,
Clyde Francks
A large-scale population study of early life factors influencing left-handedness
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Steven N. Lisgo ,
Simon E. Fisher ,
Clyde Francks
Subtle left-right asymmetry of gene expression profiles in embryonic and foetal human brains
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Flip Mulder,
Jessica van Setten,
Ruben van ‘t Slot,
Ruben van 't Slot,
Abdullah Al-Rubaish,
Abdullah M. Alshehri,
Khalid Al Faraidy,
Khalid Al Faraidy,
Abdullah Al-Ali,
Mohammed Al-Madan,
Issa Al Aqaili,
Issa Al Aqaili,
Emmanuel Larbi,
Rudaynah Al-Ali
and 4 other authors
Exome-Wide Association Analysis of Coronary Artery Disease in the Kingdom of Saudi Arabia Population
Download from dx.doi.org
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Carolien G. F. de Kovel ,
Felix Rosenow,
Bobby P. C. Koeleman,
Gregor Kuhlenbäumer,
Liron Sheintuch,
Ronel Veksler,
Alon Friedman,
Zaid Afawi,
Ingo Helbig
Download from pubman.mpdl.mpg.de
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Sarah Weckhuysen,
Bob Asselbergh,
Thomas Geuens,
Tine Deconinck,
Abdelkrim Azmi,
Patrick May ,
Eva Brilstra,
Felicitas Becker,
Nina Barisic,
Dana Craiu,
Kees P. J. Braun,
Dennis Lal,
Holger Thiele
and 11 other authors
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Loretta van Iterson,
Robert J. Lamberts,
Josemir W. Sander,
Dick Lindhout ,
Bobby P. C. Koeleman
Complex SCN8A DNA-abnormalities in an individual with therapy resistant absence epilepsy
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Marjan van Kempen,
Maartje Boon,
Joost Nicolai,
Carolien G. de Kovel ,
Eva H. Brilstra,
Bobby P. C. Koeleman
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Maartje Boon,
Joost Nicolai,
Carolien G. de Kovel ,
G. De Kovel,
Eva H. Brilstra
and 1 other authors
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,
Hans Stroink
and 12 other authors
Effect of vaccinations on seizure risk and disease course in Dravet syndrome
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Bobby P. C. Koeleman,
Désirée M. F. M. van der Heijde,
Tom W. J. Huizinga,
René E. M. Toes,
Jeanine J. Houwing-Duistermaat ,
Caroline Ospelt,
Björn Svensson,
Annette H. M. van der Helm-Van Mil
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Clinical and genetic analysis of a family with two rare reflex epilepsies
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Miriam H. Meisler,
Eva H. Brilstra,
Frederique M. C. van Berkestijn,
Ruben van ‘t Slot,
Stef van Lieshout,
Isaac J. Nijman,
Janelle E. O’Brien,
Michael F. Hammer,
Mark Estacion,
Stephen G. Waxman,
Sulayman D. Dib-Hajj,
Bobby P. C. Koeleman
Characterization of a de novo SCN8A mutation in a patient with epileptic encephalopathy
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,
Jansen Fe,
Vermeer de Bondt Pe,
Marjan J. A. van Kempen,
de Kovel Cg,
van Kempen Mj,
Dick Lindhout ,
Nicoline A. T. van der Maas,
Nine V. A. M. Knoers,
Knoers Nv,
van der Maas Na
and 2 other authors
Etiologies for Seizures Around the Time of Vaccination
Download from pediatrics.aappublications.org
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Carolien G. F. de Kovel ,
Rima Nabbout,
Brilstra Eh,
Claude Cancès,
Dorothée Ville,
Eva H. Brilstra,
Giuseppe Gobbi,
Emmanuel Raffo,
Delphine Bouteiller,
Yannick Marie
and 63 other authors
De novo mutations in HCN1 cause early infantile epileptic encephalopathy
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Clément Huneau,
Felicitas Becker,
Hiltrud Muhle,
Arvid Suls,
Johannes R. Lemke,
Carolien G. F. de Kovel ,
Holger Thiele,
Kathryn Konrad,
Amit Kawalia,
Mohammad R. Toliat,
Thomas Sander
and 33 other authors
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes
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The canonical equation of adaptive dynamics for Mendelian diploids and haplo-diploids
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