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	Title	Authors / Editors	Date
unige:145886	Usefulness of genetic testing in sudden cardiac arrest survivors with or without previous clinical evidence of heart disease	Asatryan, Babken; Schaller, André; Seiler, Jens; Servatius, Helge; ... Medeiros-Domingo, Argelia	2019
unige:128287	De novo variants in neurodevelopmental disorders with epilepsy	Heyne, Henrike O; Singh, Tarjinder; Stamberger, Hannah; Abou Jamra, Rami; ... Lemke, Johannes R	2018
unige:111193	The forensic use of behavioral genetics in criminal proceedings: Case of the MAOA-L genotype	McSwiggan, Sally; Elger, Bernice Simone; Appelbaum, Paul S	2017
unige:112167	Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa	Duncan, Laramie; Yilmaz, Zeynep; Gaspar, Helena; Walters, Raymond; ... Bulik, Cynthia M	2017
unige:142388	A novel recessive RPGRIP1 mutation causing leber congenital amaurosis	Abouzeid, Hana; Othman, I S; Schorderet, D F	2016
unige:90584	Genetic studies of body mass index yield new insights for obesity biology	Locke, Adam E; Kahali, Bratati; Berndt, Sonja I; Justice, Anne E; ... Mach, François	2015
unige:89750	Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration	van der Zee, Julie	2014
unige:55188	Towards the identification of a genetic basis for Landau-Kleffner syndrome	Conroy, Judith; McGettigan, Paul A; McCreary, Dara; Shah, Naisha; ... King, Mary D	2014
unige:42274	Guidelines for investigating causality of sequence variants in human disease	MacArthur, D G; Manolio, T A; Dimmock, D P; Rehm, H L; ... Gunter, C	2014
unige:89773	ANKRD26-related thrombocytopenia and myeloid malignancies	Noris, Patrizia; Favier, Remi; Alessi, Marie-Christine; Geddis, Amy E; ... Balduini, Carlo L	2013
unige:43122	Influence of CRTC1 polymorphisms on body mass index and fat mass in psychiatric patients and the general adult population	Choong, Eva; Quteineh, Lina; Cardinaux, Jean-René; Gholam-Rezaee, Mehdi; ... Eap, Chin Bin	2013
unige:34839	Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers	Weckhuysen, Sarah; Holmgren, Philip; Hendrickx, Rik; Jansen, Anna C; ... Suls, Arvid	2013
unige:34516	Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome	Nikolaev, Sergey Igorievich; Santoni, Federico; Vannier, Anne; Falconnet, Emilie; ... Antonarakis, Stylianos	2013
unige:37947	Mutations of DEPDC5 cause autosomal dominant focal epilepsies	Ishida, Saeko; Picard, Fabienne; Rudolf, Gabrielle; Noé, Eric; ... Baulac, Stéphanie	2013
unige:45192	EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?	Lesage, Suzanne; Condroyer, Christel; Klebe, Stephan; Lohmann, Ebba; ... Brice, Alexis	2012
unige:29824	Psoriasis	Boehncke, Wolf-Henning; Mrowietz, Ulrich	2012
unige:32242	Genome-wide profiling of blood pressure in adults and children	Taal, Hendrik R; Verwoert, Germaine C; Demirkan, Ayse; Janssens, A Cecile J W; ... van Duijn, Cornelia	2012
unige:32308	Fibrinogen Gdansk: hypofibrinogenemia associated with a novel missense mutation in FGA (Ser112Pro)	Mital, Andrzej; Undas, Anetta; Neerman Arbez, Marguerite; Hellmann, Andrzej	2012
unige:37818	An integrated encyclopedia of DNA elements in the human genome	ENCODE Project Consortium	2012
unige:31209	Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus	Anderson, Beverley H; Kasher, Paul R; Mayer, Josephine	2012

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