S
She'era Medad
Publications - 6
Citations - 1085
She'era Medad is an academic researcher. The author has contributed to research in topics: Attention deficit hyperactivity disorder & Twin study. The author has an hindex of 6, co-authored 6 publications receiving 1044 citations.
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The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes.
Keeley J. Brookes,Xiaohui Xu,Wei J. Chen,Kaixin Zhou,Benjamin M. Neale,N. Lowe,R. Aneey,Barbara Franke,Michael Gill,Richard P. Ebstein,Jan K. Buitelaar,Pak C. Sham,Desmond Campbell,Joanne Knight,Penny Andreou,Marieke E. Altink,Raoul Arnold,Frits Boer,Cathelijne J. M. Buschgens,Louise Butler,Hanna Christiansen,Leonard C. Feldman,K. Fleischman,Ellen A. Fliers,Raoul Howe-Forbes,A. Goldfarb,Alexander Heise,Isabel Gabriëls,Isabelle Korn-Lubetzki,Rafaela Marco,She'era Medad,Rudolf Minderaa,Fernando Mulas,Ueli C Müller,Aisling Mulligan,K. Rabin,Nanda Rommelse,Vaheshta Sethna,J. Sorohan,Henrik Uebel,Lamprini Psychogiou,Anne Weeks,R. Barrett,Ian W. Craig,Tobias Banaschewski,Edmund J.S. Sonuga-Barke,J. Eisenberg,Jonna Kuntsi,Iris Manor,Peter McGuffin,Ana Miranda,Robert D. Oades,Robert Plomin,Herbert Roeyers,Aribert Rothenberger,Joseph A. Sergeant,Hans-Christoph Steinhausen,Eric Taylor,Margaret Thompson,Stephen V. Faraone,Philip Asherson,Lena Johansson +61 more
TL;DR: In this article, the authors examined 1038 single-nucleotide polymorphisms (SNPs) spanning 51 candidate genes involved in the regulation of neurotransmitter pathways, particularly dopamine, norepinephrine and serotonin pathways, in addition to circadian rhythm genes.
Journal ArticleDOI
Delay and reward choice in ADHD: an experimental test of the role of delay aversion.
Rafaela Marco,Ana Miranda,Wolff Schlotz,Amanda Meliá,Aisling Mulligan,Ueli C Müller,Penny Andreou,Louise Butler,Hanna Christiansen,Isabel Gabriëls,She'era Medad,Björn Albrecht,Henrik Uebel,P. Asherson,Tobias Banaschewski,Michael Gill,Jonna Kuntsi,Fernando Mulas,Robert D. Oades,Herbert Roeyers,Hans-Christoph Steinhausen,Aribert Rothenberger,Stephen V. Faraone,Edmund J.S. Sonuga-Barke +23 more
TL;DR: The results support a dual component model in which both IDIR and DAv contribute to SS choice in ADHD, and suggest SS choice may be a marker of an ADHD motivational subtype.
Journal ArticleDOI
DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage.
Wai Chen,Kaixin Zhou,Pak C. Sham,Barbara Franke,Jonna Kuntsi,Desmond Campbell,K. Fleischman,Jo Knight,Penny Andreou,Renée Arnold,Marieke E. Altink,Frits Boer,Mary Jane Boholst,Cathelijne J. M. Buschgens,Louise Butler,Hanna Christiansen,Ellen A. Fliers,Raoul Howe-Forbes,Isabel Gabriëls,Alexander Heise,Isabelle Korn-Lubetzki,Rafaela Marco,She'era Medad,Ruud B. Minderaa,Ueli C Müller,Aisling Mulligan,Lamprini Psychogiou,Nanda Rommelse,Vaheshta Sethna,Henrik Uebel,Peter McGuffin,Robert Plomin,Tobias Banaschewski,Jan K. Buitelaar,Richard P. Ebstein,Jacques Eisenberg,Michael Gill,Iris Manor,Ana Miranda,Fernando Mulas,Robert D. Oades,Herbert Roeyers,Aribert Rothenberger,Joseph A. Sergeant,Edmund J.S. Sonuga-Barke,Hans-Christoph Steinhausen,Eric Taylor,Margaret Thompson,Stephen V. Faraone,Philip Asherson +49 more
TL;DR: Data confirm the main requirement for QTL mapping of ADHD by demonstrating that narrowly defined DSM‐IV combined type probands show familial association with dimensional ADHD symptom scores amongst their siblings.
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes
Keeley J. Brookes,Xiaohui Xu,Wai Chen,Kaixin Zhou,Benjamin M. Neale,N. Lowe,R. Aneey,Barbara Franke,Michael Gill,Jan K. Buitelaar,Pak C. Sham,Desmond Campbell,Jo Knight,Penny Andreou,Marieke E. Altink,Renée Arnold,Frits Boer,Cathelijne J. M. Buschgens,Louise Butler,Hanna Christiansen,Liat Feldman,K. Fleischman,Ellen A. Fliers,Raoul Howe-Forbes,Abigail Goldfarb,Alexander Heise,Isabel Gabriëls,Isabelle Korn-Lubetzki,Rafaela Marco,She'era Medad,Ruud B. Minderaa,Fernando Mulas,Ueli C Müller,Aisling Mulligan,Karina Rabin,Nanda Rommelse,Vaheshta Sethna,Jean Sorohan,Henrik Uebel,Lamprini Psychogiou,Anne Weeks,Rebecca Barrett,Ian W. Craig,Tobias Banaschewski,Edmund J.S. Sonuga-Barke,Jacques Eisenberg,Jonna Kuntsi,Iris Manor,Peter McGuffin,Ana Miranda,Robert D. Oades,Robert Plomin,Herbert Roeyers,Aribert Rothenberger,Joseph A. Sergeant,Hans-Christoph Steinhausen,Eric Taylor,Margaret Thompson,Stephen V. Faraone,Philip Asherson,Lena Johansson +60 more
TL;DR: Examining single-nucleotide polymorphisms spanning 51 candidate genes involved in the regulation of neurotransmitter pathways, particularly dopamine, norepinephrine and serotonin pathways, found nominal significance with one or more SNPs in 18 genes, including the two most replicated findings in the literature: DRD4 and DAT1.
Journal ArticleDOI
A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.
Philip Asherson,Kaixin Zhou,Richard Anney,Barbara Franke,Barbara Franke,Jan K. Buitelaar,Richard P. Ebstein,Michael Gill,Marieke E. Altink,Raoul Arnold,Frits Boer,Keeley J. Brookes,Cathelijne J. M. Buschgens,Louise Butler,D. Cambell,Wai Chen,Hanna Christiansen,Leonard C. Feldman,K. Fleischman,Ellen A. Fliers,Raoul Howe-Forbes,A. Goldfarb,Alexander Heise,Isabel Gabriëls,Lena Johansson,I. Lubetzki,Rafaela Marco,She'era Medad,Ruud B. Minderaa,Fernando Mulas,Ulrike Müller,Aisling Mulligan,Benjamin M. Neale,Fruhling Rijsdijk,K. Rabin,Nanda Rommelse,Vaheshta Sethna,J. Sorohan,Henrik Uebel,Lamprini Psychogiou,Anne Weeks,R. Barrett,Xiaohui Xu,Tobias Banaschewski,Edmund J.S. Sonuga-Barke,J. Eisenberg,Iris Manor,Ana Miranda,Robert D. Oades,Herbert Roeyers,Aribert Rothenberger,Joseph A. Sergeant,Hans-Christoph Steinhausen,Eric Taylor,Margaret Thompson,Stephen V. Faraone +55 more
TL;DR: An affected sibling pair study of 142 narrowly defined Diagnostic and Statistical Manual of Mental Disorders, fourth edition combined type attention deficit hyperactivity disorder (ADHD) proband–sibling pairs found suggestive linkage signals on chromosomes 9 and 16, respectively.