Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rachel N. Levinson"'
Autor:
Benjamin C. Reiner, Glenn A. Doyle, Andrew E. Weller, Rachel N. Levinson, Esin Namoglu, Alicia Pigeon, Emilie Dávila Perea, Cynthia Shannon Weickert, Gustavo Turecki, Deborah C. Mash, Richard C. Crist, Wade H. Berrettini
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 10, Iss 5, Pp 1647-1655 (2020)
Long interspersed element-1 retrotransposons (LINE-1 or L1) are ∼6 kb mobile DNA elements implicated in the origins of many Mendelian and complex diseases. The actively retrotransposing L1s are mostly limited to the L1 human specific (L1Hs) transcr
Externí odkaz:
https://doaj.org/article/b4f24c25c33048b8ad162a2ff355cb5b
Autor:
Nkechi S Ojeah, Rachel N Levinson, Thomas N. Ferraro, Michael R. Sperling, Russell J. Buono, Aditya M Rao, Gabriella Arauco-Shapiro, Glenn A. Doyle, Benjamin C. Reiner, Richard C. Crist, Wade H. Berrettini, Lokesh D Shah
Publikováno v:
Epilepsia. 62:1329-1342
Objective To determine if long interspersed element-1 (L1) retrotransposons convey risk for idiopathic temporal lobe epilepsy (TLE). Methods Surgically resected temporal cortex from individuals with TLE (N = 33) and postmortem temporal cortex from in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::591d06ded29b43c770f9da78f388f57f
https://doi.org/10.1111/epi.16897
https://doi.org/10.1111/epi.16897
Autor:
Deborah C Mash, Cynthia Shannon Weickert, Gustavo Turecki, Wade H. Berrettini, Esin C. Namoglu, Rachel N Levinson, Richard C. Crist, Andrew E. Weller, Emilie Davila Perea, Glenn A. Doyle, Alicia Pigeon, Benjamin C. Reiner
Publikováno v:
G3: Genes|Genomes|Genetics
G3: Genes, Genomes, Genetics, Vol 10, Iss 5, Pp 1647-1655 (2020)
G3: Genes, Genomes, Genetics, Vol 10, Iss 5, Pp 1647-1655 (2020)
Long interspersed element-1 retrotransposons (LINE-1 or L1) are ∼6 kb mobile DNA elements implicated in the origins of many Mendelian and complex diseases. The actively retrotransposing L1s are mostly limited to the L1 human specific (L1Hs) transcr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd7946c9e693faeeda243013b7dcf3f6
https://doi.org/10.1534/g3.119.400613
https://doi.org/10.1534/g3.119.400613
Autor:
Cyndi Shannon Weickert, Aditya M Rao, Alicia Pigeon, Andrew E. Weller, Gabriella Arauco-Shapiro, Richard C. Crist, Emilie Davila Perea, Gustavo Turecki, Glenn A. Doyle, Rachel N Levinson, Benjamin C. Reiner, Esin C. Namoglu, Wade H. Berrettini
Publikováno v:
Schizophrenia Bulletin Open
Studies of the genetic heritability of schizophrenia and bipolar disorder examining single nucleotide polymorphisms (SNPs) and copy number variations have failed to explain a large portion of the genetic liability, resulting in substantial missing he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::717dd863558dfd1c89e29877deb834c6
https://pubmed.ncbi.nlm.nih.gov/34901866
https://pubmed.ncbi.nlm.nih.gov/34901866
Autor:
Esin C. Namoglu, Benjamin C. Reiner, Dávila Perea E, Rachel N Levinson, Glenn A. Doyle, Deborah C Mash, Richard C. Crist, Alicia Pigeon, Cynthia Shannon Weickert, Wade H. Berrettini, Gustavo Turecki, Andrew E. Weller, Gabriella Arauco-Shapiro
Long interspersed element-1 retrotransposons (LINE-1 or L1) are ~6 kb mobile DNA elements implicated in the origins of many Mendelian and complex diseases. The actively retrotransposing L1s are mostly limited to the L1 human specific Ta subfamily. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9e8d3536cce0a9aa6da9305381a3f19
https://doi.org/10.1101/710095
https://doi.org/10.1101/710095
Autor:
Cyndi Shannon Weickert, Gabriella Arauco-Shapiro, Thomas N. Ferraro, Richard C. Crist, Rachel N Levinson, Gustavo Turecki, Glenn A. Doyle, Rashed Nagra, Benjamin C. Reiner, Esin C. Namoglu, Wade H. Berrettini
Publikováno v:
European Neuropsychopharmacology. 29:S1259-S1260
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31109d4bc0d31aeebf936a09fca6e21f
https://doi.org/10.1016/j.euroneuro.2018.08.351
https://doi.org/10.1016/j.euroneuro.2018.08.351