| 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 |