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Medrxiv : the Preprint Server for Health Sciences
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February 26, 2024
Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing datasets
Ben Weisburd, Rakshya Sharma, Villem Pata, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 13, 2024
Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data sets
Ben Weisburd, Rakshya Sharma, Villem Pata, et al.
Nature
|
December 6, 2023
A genomic mutational constraint map using variation in 76,156 human genomes
Siwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Cell Genomics
|
February 13, 2023
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes
Konrad J Karczewski, Matthew Solomonson, Katherine R Chao, et al.
Nature
|
January 15, 2024
Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes
Siwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Nature
|
February 4, 2021
Author Correction: A structural variation reference for medical and population genetics
Ryan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Nature
|
May 29, 2020
A structural variation reference for medical and population genetics
Ryan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 3, 2026
Integrating 730,947 exome sequences with clinical literature improves gene discovery
Jeremy Guez, Julia K Goodrich, Mikhail A Moldovan, et al.
Nature
|
May 29, 2020
The mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
Nature
|
February 4, 2021
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
Medrxiv : the Preprint Server for Health Sciences
|
February 26, 2024
Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing datasets
Ben Weisburd, Rakshya Sharma, Villem Pata, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 13, 2024
Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data sets
Ben Weisburd, Rakshya Sharma, Villem Pata, et al.
Nature
|
December 6, 2023
A genomic mutational constraint map using variation in 76,156 human genomes
Siwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Cell Genomics
|
February 13, 2023
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes
Konrad J Karczewski, Matthew Solomonson, Katherine R Chao, et al.
Nature
|
January 15, 2024
Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes
Siwei Chen, Laurent C Francioli, Julia K Goodrich, et al.
Nature
|
February 4, 2021
Author Correction: A structural variation reference for medical and population genetics
Ryan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Nature
|
May 29, 2020
A structural variation reference for medical and population genetics
Ryan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 3, 2026
Integrating 730,947 exome sequences with clinical literature improves gene discovery
Jeremy Guez, Julia K Goodrich, Mikhail A Moldovan, et al.
Nature
|
May 29, 2020
The mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
Nature
|
February 4, 2021
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
Page
of 4