Rate of de novo mutations and the importance of father’s age to disease risk
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DOI: 10.1038/nature11396
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Cited by:
- Tetsushi Sadakata & Yo Shinoda & Akira Sato & Hirotoshi Iguchi & Chiaki Ishii & Makoto Matsuo & Ryosuke Yamaga & Teiichi Furuichi, 2013. "Mouse Models of Mutations and Variations in Autism Spectrum Disorder-Associated Genes: Mice Expressing Caps2/Cadps2 Copy Number and Alternative Splicing Variants," IJERPH, MDPI, vol. 10(12), pages 1-19, November.
- Anouk E. J. Janssen & Rebekka M. Koeck & Rick Essers & Ping Cao & Wanwisa Dijk & Marion Drüsedau & Jeroen Meekels & Burcu Yaldiz & Maartje Vorst & Bart Koning & Debby M. E. I. Hellebrekers & Servi J. , 2024. "Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
- Fiona A. Hagenbeek & Jana S. Hirzinger & Sophie Breunig & Susanne Bruins & Dmitry V. Kuznetsov & Kirsten Schut & Veronika V. Odintsova & Dorret I. Boomsma, 2023. "Maximizing the value of twin studies in health and behaviour," Nature Human Behaviour, Nature, vol. 7(6), pages 849-860, June.
- Kitty Sherwood & Joseph C. Ward & Ignacio Soriano & Lynn Martin & Archie Campbell & Raheleh Rahbari & Ioannis Kafetzopoulos & Duncan Sproul & Andrew Green & Julian R. Sampson & Alan Donaldson & Kai-Re, 2023. "Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
- Wafeeq Abdelaziz, Asmaa & Ibrahim Abdelmageed, Reham, 2021. "An overview of non-genetic intellectual disability among Egyptian children and adolescents," Children and Youth Services Review, Elsevier, vol. 127(C).
- Marie Bernkopf & Ummi B. Abdullah & Stephen J. Bush & Katherine A. Wood & Sahar Ghaffari & Eleni Giannoulatou & Nils Koelling & Geoffrey J. Maher & Loïc M. Thibaut & Jonathan Williams & Edward M. Blai, 2023. "Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
- Chunfeng Yun & Zhenjie Wang & Ping He & Chao Guo & Gong Chen & Xiaoying Zheng, 2016. "Prevalence and Parental Risk Factors for Speech Disability Associated with Cleft Palate in Chinese Children—A National Survey," IJERPH, MDPI, vol. 13(11), pages 1-8, November.
- Stephanie M. Bilinovich & Kristy Lewis & Barbara L. Thompson & Jeremy W. Prokop & Daniel B. Campbell, 2020. "Environmental Epigenetics of Diesel Particulate Matter Toxicogenomics," IJERPH, MDPI, vol. 17(20), pages 1-13, October.
- Hilary Cope & Edward R Ivimey-Cook & Jacob Moorad, 2022. "Triparental ageing in a laboratory population of an insect with maternal care [Male age alone predicts paternity success under sperm competition when effects of age and past mating effort are exper," Behavioral Ecology, International Society for Behavioral Ecology, vol. 33(6), pages 1123-1132.
- Dang Ton Nguyen & Hai Ha Nguyen & Thuy Duong Nguyen & Thi Thanh Hoa Nguyen & Kaoru Nakano & Kazuhiro Maejima & Aya Sasaki-Oku & Van Ba Nguyen & Duy Bac Nguyen & Bach Quang Le & Jing Hao Wong & Tatsuhi, 2018. "Whole Genome Sequencing of a Vietnamese Family from a Dioxin Contamination Hotspot Reveals Novel Variants in the Son with Undiagnosed Intellectual Disability," IJERPH, MDPI, vol. 15(12), pages 1-11, November.
- Jörn Bethune & April Kleppe & Søren Besenbacher, 2022. "A method to build extended sequence context models of point mutations and indels," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
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