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Genome Biology
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January 27, 2021
Exploiting the GTEx resources to decipher the mechanisms at GWAS loci
Alvaro N Barbeira, Rodrigo Bonazzola, Eric R Gamazon, et al.
American Journal of Human Genetics
|
September 20, 2025
Transcriptome-wide outlier approach identifies individuals with minor spliceopathies
Taylor M Arriaga, Rodrigo Mendez, Rachel A Ungar, et al.
Journal of Neurogenetics
|
May 10, 2021
Compound heterozygous <i>KCTD7</i> variants in progressive myoclonus epilepsy
Elizabeth A Burke, Morgan Sturgeon, Diane B Zastrow, et al.
HGG Advances
|
March 11, 2026
Biallelic Variants in RNU6ATAC Result in a Minor Spliceopathy Characterized by Transcriptome-Wide Minor Intron Retention Events and Short Stature with Variable Multisystem Manifestations
Rodrigo Mendez, Taylor M Arriaga, Jialan Ma, et al.
Nucleic Acids Research
|
November 17, 2007
ORegAnno: an open-access community-driven resource for regulatory annotation
Obi L Griffith, Stephen B Montgomery, Bridget Bernier, et al.
Research Square
|
January 10, 2024
ASSESSMENT OF CELL SURFACE TARGETS IN METASTATIC PROSTATE CANCER: EXPRESSION LANDSCAPE AND MOLECULAR CORRELATES
Azra Ajkunic, Erolcan Sayar, Martine P Roudier, 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.
European Urology
|
August 5, 2025
Neoadjuvant Pembrolizumab and Accelerated Methotrexate, Vinblastine, Doxorubicin, and Cisplatin in Nonurothelial Histologic Subtypes of Muscle-invasive Bladder Cancer: A Phase 2 Trial
Ruben Raychaudhuri, Ali Raza Khaki, Mary W Redman, et al.
Nature Genetics
|
October 19, 2023
Integrative analyses highlight functional regulatory variants associated with neuropsychiatric diseases
Margaret G Guo, David L Reynolds, Cheen E Ang, et al.
American Journal of Medical Genetics. Part A
|
April 20, 2026
De Novo Variants Associated With Autosomal Recessive Conditions: Case Series and Implications for Genetic Testing and Counseling
Annie D Niehaus, Devon E Bonner, Jennefer Carter, et al.
Page
of 69
Search research articles
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Showing results (621-630 of 683) with videos related to
Sort By:
Page
of 69
Genome Biology
|
January 27, 2021
Exploiting the GTEx resources to decipher the mechanisms at GWAS loci
Alvaro N Barbeira, Rodrigo Bonazzola, Eric R Gamazon, et al.
American Journal of Human Genetics
|
September 20, 2025
Transcriptome-wide outlier approach identifies individuals with minor spliceopathies
Taylor M Arriaga, Rodrigo Mendez, Rachel A Ungar, et al.
Journal of Neurogenetics
|
May 10, 2021
Compound heterozygous <i>KCTD7</i> variants in progressive myoclonus epilepsy
Elizabeth A Burke, Morgan Sturgeon, Diane B Zastrow, et al.
HGG Advances
|
March 11, 2026
Biallelic Variants in RNU6ATAC Result in a Minor Spliceopathy Characterized by Transcriptome-Wide Minor Intron Retention Events and Short Stature with Variable Multisystem Manifestations
Rodrigo Mendez, Taylor M Arriaga, Jialan Ma, et al.
Nucleic Acids Research
|
November 17, 2007
ORegAnno: an open-access community-driven resource for regulatory annotation
Obi L Griffith, Stephen B Montgomery, Bridget Bernier, et al.
Research Square
|
January 10, 2024
ASSESSMENT OF CELL SURFACE TARGETS IN METASTATIC PROSTATE CANCER: EXPRESSION LANDSCAPE AND MOLECULAR CORRELATES
Azra Ajkunic, Erolcan Sayar, Martine P Roudier, 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.
European Urology
|
August 5, 2025
Neoadjuvant Pembrolizumab and Accelerated Methotrexate, Vinblastine, Doxorubicin, and Cisplatin in Nonurothelial Histologic Subtypes of Muscle-invasive Bladder Cancer: A Phase 2 Trial
Ruben Raychaudhuri, Ali Raza Khaki, Mary W Redman, et al.
Nature Genetics
|
October 19, 2023
Integrative analyses highlight functional regulatory variants associated with neuropsychiatric diseases
Margaret G Guo, David L Reynolds, Cheen E Ang, et al.
American Journal of Medical Genetics. Part A
|
April 20, 2026
De Novo Variants Associated With Autosomal Recessive Conditions: Case Series and Implications for Genetic Testing and Counseling
Annie D Niehaus, Devon E Bonner, Jennefer Carter, et al.
Page
of 69