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Vaccine: X
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October 24, 2024
A literature review and evidence-based evaluation of the Dutch national immunisation schedule yield possibilities for improvements
A J M Pluijmaekers, A Steens, H Houweling, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 24, 2026
International Clinical Evidence-based Guideline for Kleefstra Syndrome
Arianne Bouman, Charlotte M W Gaasterland, Carla Sloof-Enthoven, et al.
HGG Advances
|
November 21, 2022
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder
Lot Snijders Blok, Jolijn Verseput, Dmitrijs Rots, et al.
Nature Communications
|
May 17, 2019
Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis
John A Lees, Bart Ferwerda, Philip H C Kremer, et al.
European Journal of Human Genetics : EJHG
|
October 20, 2025
Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision making
Daphne J Smits, Federico Ferraro, Mark Drost, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 14, 2022
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein
Elke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 2, 2022
Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature
Richard H van Jaarsveld, Jack Reilly, Marie-Claire Cornips, et al.
Blood Advances
|
February 3, 2022
Quantitative analysis of mRNA-1273 COVID-19 vaccination response in immunocompromised adult hematology patients
Sabine Haggenburg, Birgit I Lissenberg-Witte, Rob S van Binnendijk, et al.
Nature Communications
|
July 1, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity
Aleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
American Journal of Human Genetics
|
April 28, 2021
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
Dmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
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of 34
Search research articles
Search
Showing results (321-330 of 334) with videos related to
Sort By:
Page
of 34
Vaccine: X
|
October 24, 2024
A literature review and evidence-based evaluation of the Dutch national immunisation schedule yield possibilities for improvements
A J M Pluijmaekers, A Steens, H Houweling, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 24, 2026
International Clinical Evidence-based Guideline for Kleefstra Syndrome
Arianne Bouman, Charlotte M W Gaasterland, Carla Sloof-Enthoven, et al.
HGG Advances
|
November 21, 2022
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder
Lot Snijders Blok, Jolijn Verseput, Dmitrijs Rots, et al.
Nature Communications
|
May 17, 2019
Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis
John A Lees, Bart Ferwerda, Philip H C Kremer, et al.
European Journal of Human Genetics : EJHG
|
October 20, 2025
Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision making
Daphne J Smits, Federico Ferraro, Mark Drost, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 14, 2022
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein
Elke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 2, 2022
Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature
Richard H van Jaarsveld, Jack Reilly, Marie-Claire Cornips, et al.
Blood Advances
|
February 3, 2022
Quantitative analysis of mRNA-1273 COVID-19 vaccination response in immunocompromised adult hematology patients
Sabine Haggenburg, Birgit I Lissenberg-Witte, Rob S van Binnendijk, et al.
Nature Communications
|
July 1, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity
Aleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
American Journal of Human Genetics
|
April 28, 2021
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
Dmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
Page
of 34