A review of studies examining the association between genetic biomarkers (short tandem repeats and single-nucleotide polymorphisms) and risk of prostate cancer: the need for valid... by Mohammed H. Albujja, Ramachandran Vasudevan, Saleh Alghamdi, Chong P. Pei, Khairul A. Bin Mohd Ghani, Yazan Ranneh, Patimah B. Ismail

Subjects: “…Human genetics…”
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Host genetic variation and its microbiome interactions within the Human Microbiome Project by Raivo Kolde, Eric A. Franzosa, Gholamali Rahnavard, Andrew Brantley Hall, Hera Vlamakis, Christine Stevens, Mark J. Daly, Ramnik J. Xavier, Curtis Huttenhower

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Soft Law in International Governance by Paweł Kwiatkowski

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De novo KAT6B mutation causes Say–Barber–Biesecker–Young–Simpson variant of Ohdo syndrome in an Iranian boy: a case report by Behzad Davarnia, Mohammad Panahi, Bahareh Rahimi, Hassan Anari, Reza Farajollahi, Ehsan Abbaspour Rodbaneh, Farhad Jeddi

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Lymphoproliferation and hyper-IgM as the first manifestation of activated phosphoinositide 3-kinase δ syndrome: A case report by Mónica Fernandes-Pineda, Andrés F. Zea-Vera

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Mid-pass whole-genome sequencing in a Malagasy cohort uncovers body composition associations by Iman Hamid, Séverine Nantenaina Stéphie Raveloson, Germain Jules Spiral, Soanorolalao Ravelonjanahary, Brigitte Marie Raharivololona, José Mahenina Randria, Mosa Zafimaro, Tsiorimanitra Aimée Randriambola, Rota Mamimbahiny Andriantsoa, Tojo Julio Andriamahefa, Bodonomena Fitahiana Laza Rafidison, Mehreen Mughal, Anne-Katrin Emde, Melissa Hendershott, Sarah LeBaron von Baeyer, Kaja A. Wasik, Jean Freddy Ranaivoarisoa, Laura Yerges-Armstrong, Stephane E. Castel, Rindra Rakotoarivony

Subjects: “…human genetics…”
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Relating pathogenic loss-of-function mutations in humans to their evolutionary fitness costs by Ipsita Agarwal, Zachary L Fuller, Simon R Myers, Molly Przeworski

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A Nonsense Mutation in COL4A4 Gene Causing Isolated Hematuria in Either Heterozygous or Homozygous State by Cheng Yang, Yuan Song, Zhaowei Chen, Xiaohan Yuan, Xinhua Chen, Guohua Ding, Yang Guan, Mary McGrath, Chunhua Song, Yongqing Tong, Huiming Wang

Subjects: “…human genetics…”
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Whole-Genome Sequencing and Genomic Variant Analysis of Kazakh Individuals by Ulykbek Kairov, Askhat Molkenov, Aigul Sharip, Saule Rakhimova, Madina Seidualy, Arang Rhie, Ulan Kozhamkulov, Maxat Zhabagin, Jong-Il Kim, Joseph H. Lee, Joseph D. Terwilliger, Jeong-Sun Seo, Zhaxybay Zhumadilov, Zhaxybay Zhumadilov, Ainur Akilzhanova

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Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences by Liron Ganel, Lei Chen, Ryan Christ, Jagadish Vangipurapu, Erica Young, Indraniel Das, Krishna Kanchi, David Larson, Allison Regier, Haley Abel, Chul Joo Kang, Alexandra Scott, Aki Havulinna, Charleston W. K. Chiang, Susan Service, Nelson Freimer, Aarno Palotie, Samuli Ripatti, Johanna Kuusisto, Michael Boehnke, Markku Laakso, Adam Locke, Nathan O. Stitziel, Ira M. Hall

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Editorial: Methods in applied genetic epidemiology 2022 by Qi Guo, Christopher Neal Foley, Christopher Neal Foley, Zhana Kuncheva, Zhana Kuncheva

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Inheritance of Hypertrichosis Pinnae Auris-A Review of Literature by Neha Baryah, Kewal Krishan, Sanjeev Puri, Tanuj Kanchan

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Corrigendum: Parental Somatic Mosaicism Uncovers Inheritance of an Apparently De Novo GFAP Mutation by Alice Grossi, Federico Morelli, Marco Di Duca, Francesco Caroli, Isabella Moroni, Davide Tonduti, Tiziana Bachetti, Tiziana Bachetti, Isabella Ceccherini

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History of medical genetics in South Africa by Jennifer G. Kromberg, Grietje de Jong

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The Implication of Stem Cell Therapy in Cleft Lip and Palate and Other Craniofacial Anomalies – A Literature Review by Leelan Kanwal, Mariam Khawaja, Wafa Idrees, Rashna Hoshang Sukhia, Mubassar Fida

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LoFTK: a framework for fully automated calculation of predicted Loss-of-Function variants and genes by Abdulrahman Alasiri, Konrad J. Karczewski, Brian Cole, Bao-Li Loza, Jason H. Moore, Sander W. van der Laan, Folkert W. Asselbergs, Brendan J. Keating, Jessica van Setten

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Results of targeted sequencing of the <i>PRL, PRLR, PRLHR</i> genes in young women with non-tumor hyperprolactinemia by E. V. Shakhtshneider, D. E. Ivanoshchuk, S. M. Voevoda, O. D. Rymar

Subjects: “…human genetics…”
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Las mutaciones inestables, nuevo reto para el consejo genético de enfermedades hereditarias by Patricia Cuenca, Fernando Morales

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The medieval Mongolian roots of Y-chromosomal lineages from South Kazakhstan by Maxat Zhabagin, Zhaxylyk Sabitov, Pavel Tarlykov, Inkar Tazhigulova, Zukhra Junissova, Dauren Yerezhepov, Rakhmetolla Akilzhanov, Elena Zholdybayeva, Lan-Hai Wei, Ainur Akilzhanova, Oleg Balanovsky, Elena Balanovska

Subjects: “…Human genetics…”
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Mobilizing mutations: human genetics in the age of patient advocacy: by Daniel Navon, Chicago, University of Chicago Press, 2019, 384 pp., $40.00 (Cloth) $10.00 to $40.00 (E-book), ISBN: 9780226638096 by Aviad E. Raz

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