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Nature Communications
|
October 2, 2022
XPF activates break-induced telomere synthesis
Chia-Yu Guh, Hong-Jhih Shen, Liv WeiChien Chen, et al.
Journal of Lipid Research
|
April 23, 2022
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia
Weilai Dong, Karen H Y Wong, Youbin Liu, et al.
Journal of Medical Genetics
|
April 22, 2011
Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1
Anne M Slavotinek, Sergio E Baranzini, Denny Schanze, et al.
JAMA Neurology
|
August 12, 2014
Effects of the absence of apolipoprotein e on lipoproteins, neurocognitive function, and retinal function
Angel C Y Mak, Clive R Pullinger, Ling Fung Tang, et al.
Genome Biology
|
December 3, 2017
OMSV enables accurate and comprehensive identification of large structural variations from nanochannel-based single-molecule optical maps
Le Li, Alden King-Yung Leung, Tsz-Piu Kwok, et al.
Nature Communications
|
October 31, 2020
Towards a reference genome that captures global genetic diversity
Karen H Y Wong, Walfred Ma, Chun-Yu Wei, et al.
Nature Communications
|
March 6, 2019
Genome maps across 26 human populations reveal population-specific patterns of structural variation
Michal Levy-Sakin, Steven Pastor, Yulia Mostovoy, et al.
JACC. Cardiooncology
|
January 11, 2024
Cardiovascular Events After Hematopoietic Stem Cell Transplant: Incidence and Risk Factors
Alexi Vasbinder, Christopher W Hoeger, Tonimarie Catalan, et al.
Journal of the American Heart Association
|
December 29, 2023
Cardiovascular Risk Stratification of Patients Undergoing Hematopoietic Stem Cell Transplantation: The CARE-BMT Risk Score
Alexi Vasbinder, Tonimarie Catalan, Elizabeth Anderson, et al.
Epilepsia
|
June 4, 2025
Harvard Electroencephalography Database: A comprehensive clinical electroencephalographic resource from four Boston hospitals
Chenxi Sun, Jin Jing, Niels Turley, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
Nature Communications
|
October 2, 2022
XPF activates break-induced telomere synthesis
Chia-Yu Guh, Hong-Jhih Shen, Liv WeiChien Chen, et al.
Journal of Lipid Research
|
April 23, 2022
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia
Weilai Dong, Karen H Y Wong, Youbin Liu, et al.
Journal of Medical Genetics
|
April 22, 2011
Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1
Anne M Slavotinek, Sergio E Baranzini, Denny Schanze, et al.
JAMA Neurology
|
August 12, 2014
Effects of the absence of apolipoprotein e on lipoproteins, neurocognitive function, and retinal function
Angel C Y Mak, Clive R Pullinger, Ling Fung Tang, et al.
Genome Biology
|
December 3, 2017
OMSV enables accurate and comprehensive identification of large structural variations from nanochannel-based single-molecule optical maps
Le Li, Alden King-Yung Leung, Tsz-Piu Kwok, et al.
Nature Communications
|
October 31, 2020
Towards a reference genome that captures global genetic diversity
Karen H Y Wong, Walfred Ma, Chun-Yu Wei, et al.
Nature Communications
|
March 6, 2019
Genome maps across 26 human populations reveal population-specific patterns of structural variation
Michal Levy-Sakin, Steven Pastor, Yulia Mostovoy, et al.
JACC. Cardiooncology
|
January 11, 2024
Cardiovascular Events After Hematopoietic Stem Cell Transplant: Incidence and Risk Factors
Alexi Vasbinder, Christopher W Hoeger, Tonimarie Catalan, et al.
Journal of the American Heart Association
|
December 29, 2023
Cardiovascular Risk Stratification of Patients Undergoing Hematopoietic Stem Cell Transplantation: The CARE-BMT Risk Score
Alexi Vasbinder, Tonimarie Catalan, Elizabeth Anderson, et al.
Epilepsia
|
June 4, 2025
Harvard Electroencephalography Database: A comprehensive clinical electroencephalographic resource from four Boston hospitals
Chenxi Sun, Jin Jing, Niels Turley, et al.
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of 5