Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kathryn R, Lowe"'
Autor:
Sek Won Kong, Christin D Collins, Yuko Shimizu-Motohashi, Ingrid A Holm, Malcolm G Campbell, In-Hee Lee, Stephanie J Brewster, Ellen Hanson, Heather K Harris, Kathryn R Lowe, Adrianna Saada, Andrea Mora, Kimberly Madison, Rachel Hundley, Jessica Egan, Jillian McCarthy, Ally Eran, Michal Galdzicki, Leonard Rappaport, Louis M Kunkel, Isaac S Kohane
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e49475 (2012)
Autism Spectrum Disorders (ASD) is a spectrum of highly heritable neurodevelopmental disorders in which known mutations contribute to disease risk in 20% of cases. Here, we report the results of the largest blood transcriptome study to date that aims
Externí odkaz:
https://doaj.org/article/bd29388a58af4c0ebd3d7730491c691a
Autor:
Adrianna Saada, Ally Eran, Jessica Egan, Christin D. Collins, Heather K. Harris, Michal Galdzicki, Rachel J. Hundley, Stephanie J. Brewster, Ellen Hanson, Ingrid A. Holm, Kimberly Madison, Sek Won Kong, Louis M. Kunkel, Yuko Shimizu-Motohashi, Leonard Rappaport, Kathryn R. Lowe, Isaac S. Kohane, In-Hee Lee, Andrea Mora, Jillian McCarthy, Malcolm G. Campbell
Publikováno v:
PLoS ONE
PLoS ONE, Vol 7, Iss 12, p e49475 (2012)
PLoS ONE, Vol 7, Iss 12, p e49475 (2012)
Autism Spectrum Disorders (ASD) is a spectrum of highly heritable neurodevelopmental disorders in which known mutations contribute to disease risk in 20% of cases. Here, we report the results of the largest blood transcriptome study to date that aims
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cde3ca6bb4916d66f4c4438af92630bd
http://europepmc.org/articles/PMC3515554
http://europepmc.org/articles/PMC3515554
Autor:
Yiping, Shen, Kira A, Dies, Ingrid A, Holm, Carolyn, Bridgemohan, Magdi M, Sobeih, Elizabeth B, Caronna, Karen J, Miller, Jean A, Frazier, Iris, Silverstein, Jonathan, Picker, Laura, Weissman, Peter, Raffalli, Shafali, Jeste, Laurie A, Demmer, Heather K, Peters, Stephanie J, Brewster, Sara J, Kowalczyk, Beth, Rosen-Sheidley, Caroline, McGowan, Andrew W, Duda, Sharyn A, Lincoln, Kathryn R, Lowe, Alison, Schonwald, Michael, Robbins, Fuki, Hisama, Robert, Wolff, Ronald, Becker, Ramzi, Nasir, David K, Urion, Jeff M, Milunsky, Leonard, Rappaport, James F, Gusella, Christopher A, Walsh, Bai-Lin, Wu, David T, Miller, Ludwig, von Hahn
Publikováno v:
Pediatrics. 125(4)
BACKGROUND: Multiple lines of evidence indicate a strong genetic contribution to autism spectrum disorders (ASDs). Current guidelines for clinical genetic testing recommend a G-banded karyotype to detect chromosomal abnormalities and fragile X DNA te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cad6e0eb3b8ab6303ba6e17b66cb3489
https://pubmed.ncbi.nlm.nih.gov/20231187
https://pubmed.ncbi.nlm.nih.gov/20231187