Pewarisan Sifat Ketahanan Tanaman Melon (Cucumis melo L.) terhadap Powdery Mildew (Podosphaera xanthii (Castag.) Braun et Shishkoff) by Budi Setiadi Daryono, Muhammad Taufiq Qurrohman

Subjects: Get full text

Confirmation and inheritance of glufosinate resistance in an Amaranthus palmeri population from North Carolina by Eric A. L. Jones, Jeffrey C. Dunne, Charles W. Cahoon, Katherine M. Jennings, Ramon G. Leon, Wesley J. Everman

Subjects: Get full text

Multivariate Adaptive Regression Splines Enhance Genomic Prediction of Non-Additive Traits by Maurício de Oliveira Celeri, Weverton Gomes da Costa, Ana Carolina Campana Nascimento, Camila Ferreira Azevedo, Cosme Damião Cruz, Vitor Seiti Sagae, Moysés Nascimento

Subjects: Get full text

Oligogenic heterozygous inheritance of sperm abnormalities in mouse by Guillaume Martinez, Charles Coutton, Corinne Loeuillet, Caroline Cazin, Jana Muroňová, Magalie Boguenet, Emeline Lambert, Magali Dhellemmes, Geneviève Chevalier, Jean-Pascal Hograindleur, Charline Vilpreux, Yasmine Neirijnck, Zine-Eddine Kherraf, Jessica Escoffier, Serge Nef, Pierre F Ray, Christophe Arnoult

Subjects: Get full text

New findings in oligogenic inheritance of congenital hypogonadotropic hypogonadism by Agnieszka Gach, Iwona Pinkier, Urszula Wysocka, Kinga Sałacińska, Dominik Salachna, Maria Szarras-Czapnik, Aleksandra Pietrzyk, Agata Sakowicz, Anna Nykel, Lena Rutkowska, Magda Rybak-Krzyszkowska, Magda Socha, Aleksander Jamsheer, Lucjusz Jakubowski

Subjects: Get full text

Editorial: Monogenic vs. Oligogenic Reclassification by Olfa Messaoud, Atanu Kumar Dutta, Mario Reynaldo Cornejo-Olivas, Mario Reynaldo Cornejo-Olivas, Zahurul A. Bhuiyan

Subjects: Get full text

De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathies by Nirmal Vadgama, Mohamed Ameen, Laksshman Sundaram, Sadhana Gaddam, Genomics England Research Consortium, Casey Gifford, Jamal Nasir, Ioannis Karakikes

Subjects: Get full text

Quadruple genetic variants in a sporadic ALS patient by Rüstem Yilmaz, Kanchi Weishaupt, Ivan Valkadinov, Antje Knehr, David Brenner, Jochen H. Weishaupt

Subjects: Get full text

Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome by Elizabeth E. Blue, Janson J. White, Michael K. Dush, William W. Gordon, Brent H. Wyatt, Peter White, Colby T. Marvin, Emmi Helle, Tiina Ojala, James R. Priest, Mary M. Jenkins, Lynn M. Almli, Jennita Reefhuis, Faith Pangilinan, Lawrence C. Brody, Kim L. McBride, Vidu Garg, Gary M. Shaw, Paul A. Romitti, Wendy N. Nembhard, Marilyn L. Browne, Martha M. Werler, Denise M. Kay, Seema Mital, Jessica X. Chong, Nanette M. Nascone-Yoder, Michael J. Bamshad

Subjects: Get full text

Oligogenic Inheritance Underlying Incomplete Penetrance of PROKR2 Mutations in Hypogonadotropic Hypogonadism by Rahma Mkaouar, Rahma Mkaouar, Lamia Cherif Ben Abdallah, Chokri Naouali, Saida Lahbib, Zinet Turki, Sahar Elouej, Yosra Bouyacoub, Maali Somai, Kenneth Mcelreavey, Anu Bashamboo, Sonia Abdelhak, Olfa Messaoud

Subjects: Get full text

Faster and more accurate pathogenic combination predictions with VarCoPP2.0 by Nassim Versbraegen, Barbara Gravel, Charlotte Nachtegael, Alexandre Renaux, Emma Verkinderen, Ann Nowé, Tom Lenaerts, Sofia Papadimitriou

Subjects: “…Oligogenic diseases…”
Get full text

Genetic and Phenotypic Characteristics of Congenital Hypothyroidism in a Chinese Cohort by Wei Long, Fang Guo, Ruen Yao, Ying Wang, Huaiyan Wang, Bin Yu, Peng Xue

Subjects: Get full text

Genetic heterogeneity in familial forms of genetic generalized epilepsy: from mono- to oligogenism by Maha Dahawi, Jean-Madeleine de Sainte Agathe, Mohamed S. Elmagzoub, Elhami A. Ahmed, Julien Buratti, Thomas Courtin, Eric Noé, Julie Bogoin, Bruno Copin, Fatima A. Elmugadam, Wasma A. Abdelgadir, Ahmed K. M. A. Ahmed, Mohamed A. Daldoum, Rayan Mamoon Ibrahim Altayeb, Mohamed Bashir, Leena Mohamed Khalid, Sahar Gamil, Sara Baldassari, Liena Elsayed, Boris Keren, Gregory Nuel, Ammar E. Ahmed, Eric Leguern

Subjects: Get full text

Oligogenic Inheritance of Monoallelic TRIP11, FKBP10, NEK1, TBX5, and NBAS Variants Leading to a Phenotype Similar to Odontochondrodysplasia by Alice Costantini, Helena Valta, Anne-Maarit Suomi, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie, Fulya Taylan, Fulya Taylan

Subjects: Get full text

Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance by Valerie Jacquemin, Nassim Versbraegen, Sarah Duerinckx, Annick Massart, Julie Soblet, Camille Perazzolo, Nicolas Deconinck, Elise Brischoux-Boucher, Anne De Leener, Nicole Revencu, Sandra Janssens, Stèphanie Moorgat, Bettina Blaumeiser, Kristiina Avela, Renaud Touraine, Imad Abou Jaoude, Kathelijn Keymolen, Pascale Saugier-Veber, Tom Lenaerts, Marc Abramowicz, Isabelle Pirson

Subjects: Get full text

Further Considerations in Childhood-Onset Hypertrophic Cardiomyopathy Genetic Testing by Michelle M. Monasky, Emanuele Micaglio, Silvia Ignaccolo, Carlo Pappone, Carlo Pappone

Subjects: Get full text

Replication of linkage of familial hypobetalipoproteinemia to chromosome 3p in six kindreds by Rosalind J. Neuman, Bo Yuan, Daniela S. Gerhard, Kuang-Yu Liu, Pin Yue, Shenghui Duan, Maurizio Averna, Gustav Schonfeld

Subjects: Get full text

Complex genetic architecture in severe hypobetalipoproteinemia by Linda R. Wang, Adam D. McIntyre, Robert A. Hegele

Subjects: Get full text

Whole exome sequencing and trio analysis to broaden the variant spectrum of genes in idiopathic hypogonadotropic hypogonadism by Jian Zhang, Shu-Yan Tang, Xiao-Bin Zhu, Peng Li, Jian-Qi Lu, Jiang-Shan Cong, Ling-Bo Wang, Feng Zhang, Zheng Li

Subjects: “…idiopathic hypogonadotropic hypogonadism; maternal inheritance; oligogenic inheritance; whole exome sequencing…”
Get full text

Commentary: Potential Links between Hepadnavirus and Bornavirus Sequences in the Host Genome and Cancer by Francesco Cetta, Maria Palmieri, Alessandra Renieri, Alessandra Renieri, Elisa Frullanti

Subjects: Get full text