Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Sergey, Kisselev"'
Autor:
Gregory L Alexander, Lusine Poghosyan, Yihong Zhao, Mollie Hobensack, Sergey Kisselev, Allison A Norful, John McHugh, Keely Wise, M Brooke Schrimpf, Ann Kolanowski, Tamanna Bhatia, Sabrina Tasnova
Publikováno v:
JMIR Research Protocols, Vol 13, p e56170 (2024)
BackgroundSurvey-driven research is a reliable method for large-scale data collection. Investigators incorporating mixed-mode survey designs report benefits for survey research including greater engagement, improved survey access, and higher response
Externí odkaz:
https://doaj.org/article/9984b506ee1e4641b0713179e3bf1ff6
Autor:
Ali G. Gharavi, Aneesha Shetty, Sergey Kisselev, Ibrahim Tawhari, Richard Gargiulo, Irtaza Usman, Susan E. Quaggin, Luisa Safar-Boueri, Vikram Aggarwal, Yahspal Kanwar, Ameen Alahmadi, Nay Seif
Publikováno v:
Journal of the American Society of Nephrology. 32:33-40
Background Studies have documented AKI with high-grade proteinuria in patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. In some patients, biopsies have revealed collapsing glomerulopathy, a distinct form of glomeru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd643d29e6ce3d3f26556cdd531b87ce
https://doi.org/10.1681/asn.2020060804
https://doi.org/10.1681/asn.2020060804
Autor:
Lorraine N Clark, Robin Chan, Rong Cheng, Xinmin Liu, Naeun Park, Nancy Parmalee, Sergey Kisselev, Etty Cortes, Paola A Torres, Gregory M Pastores, Jean P Vonsattel, Roy Alcalay, Karen Marder, Lawrence L Honig, Stanley Fahn, Richard Mayeux, Michael Shelanski, Gilbert Di Paolo, Joseph H Lee
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0125204 (2015)
Variants in GBA are associated with Lewy Body (LB) pathology. We investigated whether variants in other lysosomal storage disorder (LSD) genes also contribute to disease pathogenesis.We performed a genetic analysis of four LSD genes including GBA, HE
Externí odkaz:
https://doaj.org/article/494bdd70e05b44d699035586fa58b9f0
Autor:
Nancy S Green, Katherine L Ender, Farzana Pashankar, Catherine Driscoll, Patricia J Giardina, Craig A Mullen, Lorraine N Clark, Deepa Manwani, Jennifer Crotty, Sergey Kisselev, Kathleen A Neville, Carolyn Hoppe, Sandra Barral
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e55709 (2013)
Fetal hemoglobin level is a heritable complex trait that strongly correlates swith the clinical severity of sickle cell disease. Only few genetic loci have been identified as robustly associated with fetal hemoglobin in patients with sickle cell dise
Externí odkaz:
https://doaj.org/article/b92ea4c772dc4035bd0462f3b0f400f6
Autor:
Sergey Kisselev, Syeda Behjat Ahmad, Satoru Kudose, Thomas L. Nickolas, Pietro A. Canetta, Eric Siddall, Vivette D. D'Agati, Yonatan Peleg, Ali G. Gharavi
Publikováno v:
Kidney International Reports
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::151ad99f6f0891f34c53ebb063fde0cd
Autor:
Annie J. Lee, Deborah Pang, Sergey Kisselev, Joseph H. Lee, Warren B. Zigman, Lam Ha Dang, Lorraine N. Clark, José A. Luchsinger, Sharon J. Krinsky-McHale, Benjamin Tycko, Nicole Schupf, Wayne Silverman
Publikováno v:
Neurobiology of Aging. 56:150-158
Individuals with Down syndrome (DS) overexpress many genes on chromosome 21 due to trisomy and have high risk of dementia due to the Alzheimer's disease (AD) neuropathology. However, there is a wide range of phenotypic differences (e.g., age at onset
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3404bfa50e638ad89b0c7525389fd691
https://doi.org/10.1016/j.neurobiolaging.2017.04.018
https://doi.org/10.1016/j.neurobiolaging.2017.04.018
Autor:
Elan D. Louis, Ruth Ottman, Ashley Sawle, Iuliana Ionita-Laza, Aris Floratos, Xinmin Liu, Sergey Kisselev, Lorraine N. Clark, Nora Hernandez
Publikováno v:
European Journal of Human Genetics. 24:1009-1015
Essential tremor (ET) is one of the most common causes of tremor in humans. Despite its high heritability and prevalence, few susceptibility genes for ET have been identified. To identify ET genes, whole-exome sequencing was performed in 37 early-ons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::359e11c77246ca9bbe1b7ba981bd5f84
https://doi.org/10.1038/ejhg.2015.228
https://doi.org/10.1038/ejhg.2015.228
Autor:
Hema Liyanage, Luigi Scotto, Catherine Do, Benjamin Tycko, Owen A. O'Connor, Vundavalli V. Murty, Gopeshwar Narayan, Sergey Kisselev, Lorraine N. Clark, Allen J. Freddy, Govind Bhagat, Bachir Alobeid, Ganchimeg Ishdorj, Subhadra V. Nandula, Prakash Satwani, Dongxu Xie, David G. Savage
Publikováno v:
Genes, Chromosomes and Cancer. 52:1030-1041
PCDH10 is epigenetically inactivated in multiple tumor types; however, studies in mature lymphoid malignancies are limited. Here, we have investigated the presence of promoter hypermethylation of the PCDH10 gene in a large cohort of well-characterize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b7edf2da3b5cf90f287a4856ceeff7a
https://doi.org/10.1002/gcc.22098
https://doi.org/10.1002/gcc.22098
Autor:
Llency Rosado, Ming X. Tang, Ruth Ottman, Kevin Novak, Lucien J. Cote, Steven J. Frucht, Laura Marsh, Brad Hiner, Danna Jennings, Caroline M. Tanner, Miguel Verbitsky, Barbara Ross, William K. Scott, Stanley Fahn, Helen Mejia-Santana, Andrew Siderowf, Susan B. Bressman, Elan D. Louis, Howard Andrews, Ronald F. Pfeiffer, Joseph H. Friedman, Brian C. Rakitin, Sergey Kisselev, Roy N. Alcalay, Elise Caccappolo, Michael Rezak, Blair Ford, Lorraine N. Clark, Cynthia L. Comella, Amy Colcher, Cheryl Waters, Karen Marder, Susan F. Mickel, Martha Nance
Publikováno v:
Journal of the International Neuropsychological Society. 17:91-100
The cognitive profile of early onset Parkinson’s disease (EOPD) has not been clearly defined. Mutations in the parkin gene are the most common genetic risk factor for EOPD and may offer information about the neuropsychological pattern of performanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e867c384f4661459f47a33ee84fa1da7
https://doi.org/10.1017/s1355617710001190
https://doi.org/10.1017/s1355617710001190
Publikováno v:
European Journal of Human Genetics. 18:838-843
A marker in the LINGO1 gene, rs9652490, showing significant genome-wide association with essential tremor (ET), was recently reported in an Icelandic population. To replicate this association in an independent population from North America, we genoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14737700302d7dac4a47c94b7ff42d61
https://doi.org/10.1038/ejhg.2010.27
https://doi.org/10.1038/ejhg.2010.27