Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Shengru, Guo"'
Autor:
Stephanie Bivona, Mustafa Tekin, Guney Bademci, Carson Smith, LeShon Peart, Brittney Johnson, Joanna Gonzalez, Nicholas Borja, Paulo Borjas Mendoza, Irman Forghani, Deborah Barbouth, Kumarie Latchman, Willa Thorson, Shengru Guo, Stephan Zuchner
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100150- (2023)
Externí odkaz:
https://doaj.org/article/c8aa0841127942399e8f99339e00529f
Autor:
Guney Bademci, Stephanie Bivona, LeShon Peart, Brittney Johnson, Joanna Gonzalez, Nicholas Borja, Paulo Borjas Mendoza, Irman Forghani, Deborah Barbouth, Kumarie Latchman, Willa Thorson, Shengru Guo, Carson Smith, Stephan Zuchner, Mustafa Tekin
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100707- (2023)
Externí odkaz:
https://doaj.org/article/f83e52f4765d42f396ee5f4eeeb65a82
Autor:
Nicholas Borja, Stephanie Bivona, Lé Shon Peart, Brittany Johnson, Joanna Gonzalez, Deborah Barbouth, Henry Moore, Shengru Guo, Undiagnosed Disease Network, Guney Bademci, Mustafa Tekin
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 4, Pp n/a-n/a (2022)
Abstract Neurodegenerative disorders and leukodystrophies are progressive neurologic conditions that can occur following the disruption of intricately coordinated patterns of gene expression. Exome sequencing has been adopted as an effective diagnost
Externí odkaz:
https://doaj.org/article/1b08c77a7c474c08a9361a04c9209c80
Autor:
Nicole D. Dueker, Shengru Guo, Ashley Beecham, Liyong Wang, Susan H. Blanton, Marco R. Di Tullio, Tatjana Rundek, Ralph L. Sacco
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 8, Iss 2, Pp 659-668 (2018)
Increased left ventricular mass (LVM) is an intermediate phenotype for cardiovascular disease (CVD) and a predictor of stroke. Using families from the Dominican Republic, we have previously shown LVM to be heritable and found evidence for linkage to
Externí odkaz:
https://doaj.org/article/a3148870bc894c39b0c987856e68f233
Autor:
Memoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, Shengru Guo, Ahmet Mutlu, Mahmut Tayyar Kalcioglu, Serhat Seyhan, Claudia Carranza, Murtaza Bonyadi, Nejat Mahdieh, Muzeyyen Yildirim-Baylan, Erick Figueroa-Ildefonso, Ozgul Alper, Tahir Atik, Abdurrahman Ayral, Nazim Bozan, Burhan Balta, Christian Rivas, Gabrielle N. Manzoli, Fabiola Huesca-Hernandez, Raja A. H. Kuchay, Merve Durgut, Guney Bademci, Mustafa Tekin
Hearing loss (HL) is a common heterogeneous trait that involves variants in more than 200 genes. In this study, we utilized exome (ES) and genome sequencing (GS) to effectively identify the genetic cause of presumably non-syndromic HL in 322 families
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b34b9d561748a50db02b17e2cdc5635
https://hdl.handle.net/20.500.12866/13603
https://hdl.handle.net/20.500.12866/13603
Modeling gene expression on the X chromosome in the brain for transcriptome‐wide association studies
Autor:
Xueyi Zhang, Shengru Guo, Adam C. Naj, Jennifer Below, Brian W. Kunkle, Logan Dumitrescu, Eden R. Martin, William S. Bush
Publikováno v:
Alzheimer's & Dementia. 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2f2dbfaf28a3ee2c2b309be4d43a993
https://doi.org/10.1002/alz.063533
https://doi.org/10.1002/alz.063533
Autor:
William K Scott, Felix Mba Medie, Felicia Ruffin, Batu K Sharma-Kuinkel, Derek D Cyr, Shengru Guo, Derek M Dykxhoorn, Robert L Skov, Niels E Bruun, Anders Dahl, Christian J Lerche, Andreas Petersen, Anders Rhod Larsen, Trine Kiilerich Lauridsen, Helle Krogh Johansen, Henrik Ullum, Erik Sørensen, Christian Hassager, Henning Bundgaard, Henrik C Schønheyder, Christian Torp-Pedersen, Louise Bruun Østergaard, Magnus Arpi, Flemming Rosenvinge, Lise T Erikstrup, Mahtab Chehri, Peter Søgaard, Paal S Andersen, Vance G Fowler
Publikováno v:
PLoS Genetics, Vol 14, Iss 10, p e1007667 (2018)
The role of host genetic variation in the development of complicated Staphylococcus aureus bacteremia (SAB) is poorly understood. We used whole exome sequencing (WES) to examine the cumulative effect of coding variants in each gene on risk of complic
Externí odkaz:
https://doaj.org/article/732cc361c3a74e8298dbd8c97b1db05c
Autor:
Megan McSherry, Katherine E Masih, Nursel H Elcioglu, Pelin Celik, Ozge Balci, Filiz Basak Cengiz, Daniella Nunez, Claire J Sineni, Serhat Seyhan, Defne Kocaoglu, Shengru Guo, Duygu Duman, Guney Bademci, Mustafa Tekin
Publikováno v:
PLoS ONE, Vol 13, Iss 11, p e0208324 (2018)
The etiology of intellectual disability (ID) is heterogeneous including a variety of genetic and environmental causes. Historically, most research has not focused on autosomal recessive ID (ARID), which is a significant cause of ID, particularly in a
Externí odkaz:
https://doaj.org/article/2b4a57a74b444ecdad297240d83a1197
Autor:
J. Michael Bailey, Alan R. Sanders, Gerulf Rieger, Gary W. Beecham, Shengru Guo, Khytam Dawood, Alana B. Kolundzija, Eden R. Martin, Ritesha S Krishnappa
Publikováno v:
Archives of Sexual Behavior
Male sexual orientation is influenced by environmental and complex genetic factors. Childhood gender nonconformity (CGN) is one of the strongest correlates of homosexuality with substantial familiality. We studied brothers in families with two or mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7f8d3dc72e34b07b132cfa45642345e
https://doi.org/10.1007/s10508-021-02146-x
https://doi.org/10.1007/s10508-021-02146-x
Autor:
Alan R. Sanders, Brendan P. Zietsch, Karin J. H. Verweij, Robert Maier, Shengru Guo, Abdel Abdellaoui, Gary W. Beecham, Niklas Långström, Morgan J. Sidari, Eden R. Martin
Publikováno v:
Nature Human Behaviour, 5(9), 1251-1258. Nature Publishing Group
Human same-sex sexual behaviour (SSB) is heritable, confers no immediately obvious direct reproductive or survival benefit and can divert mating effort from reproductive opportunities. This presents a Darwinian paradox: why has SSB been maintained de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df1166fc8d6a24de620fa72a2a6432e6
https://doi.org/10.1038/s41562-021-01168-8
https://doi.org/10.1038/s41562-021-01168-8