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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population.

Authors :Ganna A , Genovese G , Howrigan DP , Byrnes A , Kurki M , Zekavat SM , Whelan CW , Kals M , Nivard MG , Bloemendal A , Bloom JM , Goldstein JI , Poterba T , Seed C , Handsaker RE , Natarajan P , Mägi R , Gage D , Robinson EB , Metspalu A , Salomaa V , Suvisaari J , Purcell SM , Sklar P , Kathiresan S , Daly MJ , McCarroll SA , Sullivan PF , Palotie A , Esko T , Hultman C , Neale BM
Published On :2016 Dec
Journal Article


Recombinant human bone morphogenetic protein 2 outcomes for maxillary sinus floor augmentation: a systematic review and meta-analysis.

Authors :Lin GH , Lim G , Chan HL , Giannobile WV , Wang HL
Published On :2016 Nov
Journal Article Meta-Analysis


Complete mitochondrial genomes of living and extinct pigeons revise the timing of the columbiform radiation.

Authors :Soares AE , Novak BJ , Haile J , Heupink TH , Fjeldså J , Gilbert MT , Poinar H , Church GM , Shapiro B
Published On :2016 Oct 26
Journal Article



High-Efficiency Transduction of Primary Human Hematopoietic Stem/Progenitor Cells by AAV6 Vectors: Strategies for Overcoming Donor-Variation and Implications in Genome Editing.

Authors :Ling C , Bhukhai K , Yin Z , Tan M , Yoder MC , Leboulch P , Payen E , Srivastava A
Published On :2016 Oct 19
Journal Article


Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis.

Authors :Ordulu Z , Kammin T , Brand H , Pillalamarri V , Redin CE , Collins RL , Blumenthal I , Hanscom C , Pereira S , Bradley I , Crandall BF , Gerrol P , Hayden MA , Hussain N , Kanengisser-Pines B , Kantarci S , Levy B , Macera MJ , Quintero-Rivera F , Spiegel E , Stevens B , Ulm JE , Warburton D , Wilkins-Haug LE , Yachelevich N , Gusella JF , Talkowski ME , Morton CC
Published On :2016 Nov 3
Journal Article


The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes.

Authors :Mao Q , Ciotlos S , Zhang RY , Ball MP , Chin R , Carnevali P , Barua N , Nguyen S , Agarwal MR , Clegg T , Connelly A , Vandewege W , Zaranek AW , Estep PW , Church GM , Drmanac R , Peters BA
Published On :2016 Oct 11
Journal Article


Discovering MicroRNA-Regulatory Modules in Multi-Dimensional Cancer Genomic Data: A Survey of Computational Methods.

Authors :Walsh CJ , Hu P , Batt J , Dos Santos CC
Published On :2016
Review Journal Article


Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.

Authors :Gormley P , Anttila V , Winsvold BS , Palta P , Esko T , Pers TH , Farh KH , Cuenca-Leon E , Muona M , Furlotte NA , Kurth T , Ingason A , McMahon G , Ligthart L , Terwindt GM , Kallela M , Freilinger TM , Ran C , Gordon SG , Stam AH , Steinberg S , Borck G , Koiranen M , Quaye L , Adams HH , Lehtimäki T , Sarin AP , Wedenoja J , Hinds DA , Buring JE , Schürks M , Ridker PM , Hrafnsdottir MG , Stefansson H , Ring SM , Hottenga JJ , Penninx BW , Färkkilä M , Artto V , Kaunisto M , Vepsäläinen S , Malik R , Heath AC , Madden PA , Martin NG , Montgomery GW , Kurki MI , Kals M , Mägi R , Pärn K , Hämäläinen E , Huang H , Byrnes AE , Franke L , Huang J , Stergiakouli E , Lee PH , Sandor C , Webber C , Cader Z , Muller-Myhsok B , Schreiber S , Meitinger T , Eriksson JG , Salomaa V , Heikkilä K , Loehrer E , Uitterlinden AG , Hofman A , van Duijn CM , Cherkas L , Pedersen LM , Stubhaug A , Nielsen CS , Männikkö M , Mihailov E , Milani L , Göbel H , Esserlind AL , Christensen AF , Hansen TF , Werge T , International Headache Genetics Consortium , Kaprio J , Aromaa AJ , Raitakari O , Ikram MA , Spector T , Järvelin MR , Metspalu A , Kubisch C , Strachan DP , Ferrari MD , Belin AC , Dichgans M , Wessman M , van den Maagdenberg AM , Zwart JA , Boomsma DI , Smith GD , Stefansson K , Eriksson N , Daly MJ , Neale BM , Olesen J , Chasman DI , Nyholt DR , Palotie A
Published On :2016 Sep 28
Journal Article Published Erratum


Rare variant association test in family-based sequencing studies.

Authors :Wang X , Zhang Z , Morris N , Cai T , Lee S , Wang C , Yu TW , Walsh CA , Lin X
Published On :2017 Nov 1
Journal Article


Characterization of candidate genes in inflammatory bowel disease-associated risk loci.

Authors :Peloquin JM , Goel G , Kong L , Huang H , Haritunians T , Sartor RB , Daly MJ , Newberry RD , McGovern DP , Yajnik V , Lira SA , Xavier RJ
Published On :2016 Aug 18
Journal Article


Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior.

Authors :Doan RN , Bae BI , Cubelos B , Chang C , Hossain AA , Al-Saad S , Mukaddes NM , Oner O , Al-Saffar M , Balkhy S , Gascon GG , Homozygosity Mapping Consortium for Autism , Nieto M , Walsh CA
Published On :2016 Oct 6
Journal Article


Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees.

Authors :Sul JH , Cade BE , Cho MH , Qiao D , Silverman EK , Redline S , Sunyaev S
Published On :2016 Oct 6
Journal Article



CDH23 Related Hearing Loss: A New Genetic Risk Factor for Semicircular Canal Dehiscence?

Authors :Noonan KY , Russo J , Shen J , Rehm H , Halbach S , Hopp E , Noon S , Hoover J , Eskey C , Saunders JE
Published On :2016 Dec
Journal Article