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Medrxiv : the Preprint Server for Health Sciences
|
May 27, 2024
MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing data
Jordan Rossen, Huwenbo Shi, Benjamin J Strober, et al.
Research Square
|
January 3, 2024
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection
Martin Jinye Zhang, Arun Durvasula, Colby Chiang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 18, 2023
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection
Martin Jinye Zhang, Arun Durvasula, Colby Chiang, et al.
Nature
|
October 13, 2017
The impact of rare variation on gene expression across tissues
Xin Li, Yungil Kim, Emily K Tsang, et al.
Cell
|
April 17, 2021
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease
Olivia M de Goede, Daniel C Nachun, Nicole M Ferraro, et al.
Nature Medicine
|
June 5, 2019
Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts
Laure Frésard, Craig Smail, Nicole M Ferraro, et al.
Science (New York, N.Y.)
|
September 11, 2020
Transcriptomic signatures across human tissues identify functional rare genetic variation
Nicole M Ferraro, Benjamin J Strober, Jonah Einson, et al.
Cell Genomics
|
October 23, 2023
The functional impact of rare variation across the regulatory cascade
Taibo Li, Nicole Ferraro, Benjamin J Strober, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 29, 2026
<i>Trans</i> -eQTLs reveal the architecture of human gene regulatory networks
C A Robert Warmerdam, Harm-Jan Westra, Adriaan van der Graaf, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Medrxiv : the Preprint Server for Health Sciences
|
May 27, 2024
MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing data
Jordan Rossen, Huwenbo Shi, Benjamin J Strober, et al.
Research Square
|
January 3, 2024
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection
Martin Jinye Zhang, Arun Durvasula, Colby Chiang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 18, 2023
Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection
Martin Jinye Zhang, Arun Durvasula, Colby Chiang, et al.
Nature
|
October 13, 2017
The impact of rare variation on gene expression across tissues
Xin Li, Yungil Kim, Emily K Tsang, et al.
Cell
|
April 17, 2021
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease
Olivia M de Goede, Daniel C Nachun, Nicole M Ferraro, et al.
Nature Medicine
|
June 5, 2019
Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts
Laure Frésard, Craig Smail, Nicole M Ferraro, et al.
Science (New York, N.Y.)
|
September 11, 2020
Transcriptomic signatures across human tissues identify functional rare genetic variation
Nicole M Ferraro, Benjamin J Strober, Jonah Einson, et al.
Cell Genomics
|
October 23, 2023
The functional impact of rare variation across the regulatory cascade
Taibo Li, Nicole Ferraro, Benjamin J Strober, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 29, 2026
<i>Trans</i> -eQTLs reveal the architecture of human gene regulatory networks
C A Robert Warmerdam, Harm-Jan Westra, Adriaan van der Graaf, et al.
Page
of 2