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Biorxiv : the Preprint Server for Biology
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April 22, 2024
The landscape of regional missense mutational intolerance quantified from 125,748 exomes
Katherine R Chao, Lily Wang, Ruchit Panchal, et al.
The Lancet. Oncology
|
July 19, 2023
Common Sense Oncology: outcomes that matter
Christopher M Booth, Manju Sengar, Aaron Goodman, et al.
Circulation
|
March 7, 2025
Clinical Outcomes With Normothermic Pulsatile Organ Perfusion in Heart Transplantation: A Report From the OCS Heart Perfusion Registry
Josef Stehlik, Maryjane A Farr, Mandeep R Mehra, 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.
Medrxiv : the Preprint Server for Health Sciences
|
May 25, 2026
Systematic common and rare variant association testing in 392,030 whole genomes in <i>All of Us</i>
Wenhan Lu, Robert J Carroll, Matthew Solomonson, et al.
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Search research articles
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Showing results (81-90 of 85) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 85 results.
Biorxiv : the Preprint Server for Biology
|
April 22, 2024
The landscape of regional missense mutational intolerance quantified from 125,748 exomes
Katherine R Chao, Lily Wang, Ruchit Panchal, et al.
The Lancet. Oncology
|
July 19, 2023
Common Sense Oncology: outcomes that matter
Christopher M Booth, Manju Sengar, Aaron Goodman, et al.
Circulation
|
March 7, 2025
Clinical Outcomes With Normothermic Pulsatile Organ Perfusion in Heart Transplantation: A Report From the OCS Heart Perfusion Registry
Josef Stehlik, Maryjane A Farr, Mandeep R Mehra, 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.
Medrxiv : the Preprint Server for Health Sciences
|
May 25, 2026
Systematic common and rare variant association testing in 392,030 whole genomes in <i>All of Us</i>
Wenhan Lu, Robert J Carroll, Matthew Solomonson, et al.
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