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DEFINE_ME
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Osman El-Maarri, Alexander Olek, Basak Balaban, Markus Montag, Hans van der Ven, Bulent Urman, Klaus Olek, S. Hande Caglayan, Jörn Walter, Johannes Oldenburg
Education
De novo variants in neurodevelopmental disorders with epilepsy -...
kclpure.kcl.ac.uk
... Rami and Hande Caglayan and Dana Craiu and {De Jonghe}, Peter and Renzo Guerrini and Helbig, {Katherine L.} and Koeleman, {Bobby P.C.} and Kosmicki, ... › portal › publications › export
Books & Literature
Les pierres de notre bien-être selon Hildegarde de Bingen
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Hande Caglayan marked it as to-read. Mar 11, · Erine is currently reading it. Oct 09, · new topic · Discuss This Book. There are no discussion ... › book › show ›
Related Documents
Genome-wide association analysis of genetic generalized epilepsies...
academic.oup.com
by EPICURE Consortium · · Cited by 137 — Hande Caglayan Department of Molecular Biology and Genetics. ,. Bogazici University. ,. Istanbul. ,. Turkey. Search for other works by this author on:. › hmg › article-abstract
KCNQ2-POLYMORPHISM-ANALYSIS-IN-IDIOPATHIC ...
www.aesnet.org
7 Dec — Kadriye Agan, Hande Caglayan, Canan Aykut- Bingol. Neurology, Marmara University, Faculty of Medicine, Istanbul, Turkey; Molecular Genetics, ... › abstractslisting › kcnq2-polym...
Scientific Publications
DFG GEPRIS - Professor Dr. Hande Caglayan
gepris.dfg.de
Professor Dr. Hande Caglayan, Bogazici University, Bebek, Istanbul, Türkei.
Gene family information facilitates variant interpretation and...
genomemedicine.biomedcentral.com
by D Lal · · Cited by 18 — Members of the EuroEPINOMICS-RES Consortium: Rudi Balling, Nina Barisic, Stéphanie Baulac, Hande Caglayan, Dana C. Craiu, Peter De Jonghe, ... › articles
Familial and sporadic 15q13.3 microdeletions in idiopathic...
www.ikmb.uni-kiel.de
ikmb - Institut für ... sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: ... Obermeier, Michael Wittig, Andre Franke, Hande Caglayan ...
Genome-wide association analysis of genetic generalized epilepsies...
www.ikmb.uni-kiel.de
... Arvid Suls, Katrin Smets, Peter De Jonghe, Albena Jordanova, Hande Caglayan, Zuhal Yapici, Destina A Yalcin, Betul Baykan, Nerses Bebek, Ugur Ozbek, ...
Publications
Familial and sporadic 15q13.3 microdeletions in idiopathic...
www.biomedsearch.com
10 Jul Marta A Bayly; Susannah Bellows; Costin Leu; Holger Trucks; Tanja Obermeier; Michael Wittig; Andre Franke; Hande Caglayan; Zuhal Yapici; ...
Video & Audio
hande caglayan - YouTube
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Reports & Statements
Application of rare variant transmission disequilibrium tests to...
www.nature.com
Rudi Balling, Nina Barisic, Stéphanie Baulac, Hande Caglayan, Dana Craiu, Peter De Jonghe, Christel Depienne, Renzo Guerrini, Ingo Helbig, ...
De novo variants in neurodevelopmental disorders with epilepsy |...
www.nature.com
25 Jun — Hande Caglayan. 'Carol Davila' University of Medicine Bucharest, Department of Clinical Neurosciences (No. 6), Pediatric Neurology Clinic, ... › ... › nature genetics › analyses
Miscellaneous
https://www.linkedin.com › pub › hande-caglayanhande caglayan - Turkey | Professional Profile | LinkedIn
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View hande caglayan's profile on LinkedIn, the world's largest professional community. hande's education is listed on their profile. See the complete profile on ...
Hande Caglayan | LinkedIn
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View Hande Caglayan's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Hande Caglayan discover ...
Hande Caglayan Lab - Groups - Yahoo
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#111. This message has attachments. View First Topic Go to View Last Topic. Loading of total 111 messages. Hande Caglayan Lab - Yahoo Groups.
Hande Caglayan Lab - Yahoo Groups
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Hande Caglayan Lab is a Public Group with 6 members. Hande Caglayan Lab. Public Group,; 6 members. Primary Navigation. Conversations; Photos; Files ...
Search Results - Caglayan, S. Hande - Katalog K.UTB
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Authors: El-Maarri, Osman; Olek, Alexander; Balaban, Basak; Montag, Markus; van der Ven, Hans; Urman, Bulent; Olek, Klaus; Hande Caglayan, S.; Walter, Jörn; ... › EDS › Search
De novo variants in neurodevelopmental disorders with epilepsy -...
go.gale.com
Author(s): Henrike O. Heyne , Tarjinder Singh 2 4 , Hannah Stamberger , Rami Abou Jamra 1 , Hande Caglayan 8 , Dana Craiu 9 , Peter De Jonghe ...
De novo variants in neurodevelopmental disorders with epilepsy —...
researchportal.helsinki.fi
EuroEPINOMICS- RES Consortium, Henrike O. Heyne, Tarjinder Singh, Hannah Stamberger, Rami Abou Jamra, Hande Caglayan, Dana Craiu, Peter De ...
Altmetric – De Novo Mutations in Synaptic Transmission Genes...
www.altmetric.com
Silke Appenzeller, Rudi Balling, Nina Barisic, Stéphanie Baulac, Hande Caglayan, Dana Craiu, Peter De Jonghe, Christel Depienne, Petia Dimova, Tania ...
Erratum: De Novo Mutations in Synaptic Transmission Genes Including...
profiles.wustl.edu
by S Appenzeller · · Cited by 252 — Silke Appenzeller, Rudi Balling, Nina Barisic, Stéphanie Baulac, Hande Caglayan, Dana Craiu, Peter De Jonghe, Christel Depienne, ... › publications › erratum-de-no...
De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause...
findanexpert.unimelb.edu.au
Silke Appenzeller, Rudi Balling, Nina Barisic, Stephanie Baulac, Hande Caglayan, Dana Craiu, Peter De Jonghe, Christel Depienne, Petia Dimova, Tania Djemie, ... › Scholarlywork
International Small Hands Academy (Fees & Reviews) Istanbul, Turkey,...
www.edarabia.com
Why International Small Hands Academy? 25,000+ Parent Reviews, Tuition Fees, Ratings, Curriculum | Kaleağası Sokak No:8 Rumelihisarı | At Small Hands Academy...
Internet Scientific Publications
ispub.com
Hande Caglayan, Ph.D Professor, Department of Molecular Biology and Genetics, Bogazici University. Ergul Berber, PhD Department of Molecular Biology and ...
De novo variants in neurodevelopmental disorders with epilepsy —...
portal.findresearcher.sdu.dk
by HO Heyne · · Cited by 155 — Henrike O. Heyne*, Tarjinder Singh, Hannah Stamberger, Rami Abou Jamra, Hande Caglayan, Dana Craiu, Peter De Jonghe, Renzo Guerrini, Katherine L. Helbig, ... › publications › de-...
Familial and sporadic 15q13.3 microdeletions in idiopathic...
researchportal.helsinki.fi
by LM Dibbens · · Cited by 233 — ... Tanja Obermeier, Michael Wittig, Andre Franke, Hande Caglayan, Zuhal Yapici, Consortium EPICURE, Thomas Sander, Evan E Eichler, Ingrid E Scheffer, ... › publications
M.S. Program in Molecular Biology and Genetics - Beşiktaş - İstanbul...
www.educaedu-turkiye.com
Yüksek lisans programları - beşiktaş biyoloji. I Head of department koyas bilge professors nazli basak nese bilgin koyas bilge...
Functional characterisation of the type 1 von Willebrand Scilit
www.scilit.net
Christine Brown, Zafer Baslar, S Hande Caglayan, David Lillicrap. Published: 1 January by. in Blood transfusion = Trasfusione del sangue. › article
Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort...
journals.plos.org
... Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada; Hande Caglayan, Department of Molecular Biology and Genetics, ...
Ph.D. Program in Molecular Biology and Genetics - Beşiktaş - İstanbul...
www.educaedu-turkiye.com
Doktora programları - beşiktaş biyoloji. I Head of department koyas bilge professors nazli basak nese bilgin koyas bilge hande...
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