Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS

Authors: Tess D. Pottinger, Joshua E. Motelow, Gundula Povysil, Cristiane A. Martins Moreno, Zhong Ren, Hemali Phatnani, The New York Genome Center ALS Sequencing Consortium, Timothy J. Aitman, Javier Santoyo-Lopez, Scottish Genomes Partnership, Hiroshi Mitsumoto, ALS COSMOS Study Group, PLS COSMOS Study Group, GTAC Investigators, David B. Goldstein, Matthew B. Harms

Source: BMC Genomics, Vol 25, Iss 1, Pp 1-11 (2024)

Subject Terms: Amyotrophic lateral sclerosis, ALS, Peripheral lateral sclerosis, PLS, Burden testing, Rare-variant analyses, Biotechnology, TP248.13-248.65, Genetics, QH426-470

File Description: electronic resource

Relation: https://doaj.org/toc/1471-2164

Access URL: https://doaj.org/article/77b804dfb5a346ffb655ea53c881d520

Ancient DNA at the edge of the world : Continental immigration and the persistence of Neolithic male lineages in Bronze Age Orkney

Authors: The Scottish Genomes Partnership, Dulias, Katharina, Foody, M. George B., Justeau, Pierre, Silva, Marina, Martiniano, Rui, Oteo-García, Gonzalo, Fichera, Alessandro, Rodrigues, Simão, Gandini, Francesca, Meynert, Alison, Donnelly, Kevin, Aitman, Timothy J., Chamberlain, Andrew, Lelong, Olivia, Kozikowski, George, Powlesland, Dominic, Waddington, Clive, Mattiangeli, Valeria, Bradley, Daniel G., Bryk, Jaroslaw, Soares, Pedro, Wilson, James F., Wilson, Graeme, Moore, Hazel, Pala, Maria, Edwards, Ceiridwen J., Richards, Martin B.

Source: Proceedings of the National Academy of Sciences of the United States of America, 2022 Feb . 119(8), 1-10.

Access URL: https://www.jstor.org/stable/27118668

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