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The Journal of Infectious Diseases
|
August 21, 2021
Clonal Hematopoiesis Is Associated With Low CD4 Nadir and Increased Residual HIV Transcriptional Activity in Virally Suppressed Individuals With HIV
Wouter A van der Heijden, Rosanne C van Deuren, Lisa van de Wijer, et al.
Frontiers in Cardiovascular Medicine
|
May 31, 2021
Pro-inflammatory Monocyte Phenotype During Acute Progression of Cerebral Small Vessel Disease
Marlies P Noz, Annemieke Ter Telgte, Kim Wiegertjes, et al.
Human Mutation
|
October 19, 2022
Using single molecule Molecular Inversion Probes as a cost-effective, high-throughput sequencing approach to target all genes and loci associated with macular diseases
Rebekkah J Hitti-Malin, Claire-Marie Dhaenens, Daan M Panneman, et al.
American Journal of Medical Genetics. Part A
|
February 28, 2012
A phenotype map for 14q32.3 terminal deletions
Hartmut Engels, Herdit M Schüler, Alexander M Zink, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 21, 2018
Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders
Roos van der Donk, Sandra Jansen, Janneke H M Schuurs-Hoeijmakers, et al.
Molecular Neurobiology
|
June 7, 2012
BDNF and DYRK1A are variable and inversely correlated in lymphoblastoid cell lines from Down syndrome patients
Asma Tlili, Alexander Hoischen, Clémentine Ripoll, et al.
Nature Genetics
|
November 16, 2010
A de novo paradigm for mental retardation
Lisenka E L M Vissers, Joep de Ligt, Christian Gilissen, et al.
Human Genetics
|
August 19, 2021
Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant
Jeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting, et al.
Human Genetics
|
October 5, 2021
Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant
Jeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting, et al.
JACC. Heart Failure
|
August 28, 2023
Clonal Hematopoiesis Has Prognostic Value in Dilated Cardiomyopathy Independent of Age and Clone Size
Maurits A Sikking, Sophie L V M Stroeks, Michiel T H M Henkens, et al.
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of 25
Search research articles
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Showing results (101-110 of 249) with videos related to
Sort By:
Page
of 25
The Journal of Infectious Diseases
|
August 21, 2021
Clonal Hematopoiesis Is Associated With Low CD4 Nadir and Increased Residual HIV Transcriptional Activity in Virally Suppressed Individuals With HIV
Wouter A van der Heijden, Rosanne C van Deuren, Lisa van de Wijer, et al.
Frontiers in Cardiovascular Medicine
|
May 31, 2021
Pro-inflammatory Monocyte Phenotype During Acute Progression of Cerebral Small Vessel Disease
Marlies P Noz, Annemieke Ter Telgte, Kim Wiegertjes, et al.
Human Mutation
|
October 19, 2022
Using single molecule Molecular Inversion Probes as a cost-effective, high-throughput sequencing approach to target all genes and loci associated with macular diseases
Rebekkah J Hitti-Malin, Claire-Marie Dhaenens, Daan M Panneman, et al.
American Journal of Medical Genetics. Part A
|
February 28, 2012
A phenotype map for 14q32.3 terminal deletions
Hartmut Engels, Herdit M Schüler, Alexander M Zink, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 21, 2018
Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders
Roos van der Donk, Sandra Jansen, Janneke H M Schuurs-Hoeijmakers, et al.
Molecular Neurobiology
|
June 7, 2012
BDNF and DYRK1A are variable and inversely correlated in lymphoblastoid cell lines from Down syndrome patients
Asma Tlili, Alexander Hoischen, Clémentine Ripoll, et al.
Nature Genetics
|
November 16, 2010
A de novo paradigm for mental retardation
Lisenka E L M Vissers, Joep de Ligt, Christian Gilissen, et al.
Human Genetics
|
August 19, 2021
Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant
Jeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting, et al.
Human Genetics
|
October 5, 2021
Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant
Jeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting, et al.
JACC. Heart Failure
|
August 28, 2023
Clonal Hematopoiesis Has Prognostic Value in Dilated Cardiomyopathy Independent of Age and Clone Size
Maurits A Sikking, Sophie L V M Stroeks, Michiel T H M Henkens, et al.
Page
of 25