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Journal of Medical Genetics
|
July 5, 2022
The role of single-cell genomics in human genetics
Varun K A Sreenivasan, Saranya Balachandran, Malte Spielmann
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
November 19, 2022
Comparative single-cell analysis of the adult heart and coronary vasculature
Saranya Balachandran, Jelena Pozojevic, Varun K A Sreenivasan, et al.
Viruses
|
January 22, 2022
Non-Random Pattern of Integration for Epstein-Barr Virus with Preference for Gene-Poor Genomic Chromosomal Regions into the Genome of Burkitt Lymphoma Cell Lines
Snjezana Janjetovic, Juliane Hinke, Saranya Balachandran, et al.
Clinical Genetics
|
January 18, 2025
Haplotype Phasing of Biallelic WNT10B Variants Using Long-Read Sequencing in Split-Hand/Foot Malformation Syndrome
Jelena Pozojevic, Naseebullah Kakar, Henrike L Sczakiel, et al.
Development (Cambridge, England)
|
January 30, 2023
Single-cell RNA-based phenotyping reveals a pivotal role of thyroid hormone receptor alpha for hypothalamic development
Varun K A Sreenivasan, Riccardo Dore, Julia Resch, et al.
American Journal of Human Genetics
|
January 16, 2024
STIGMA: Single-cell tissue-specific gene prioritization using machine learning
Saranya Balachandran, Cesar A Prada-Medina, Martin A Mensah, et al.
American Journal of Human Genetics
|
March 8, 2024
STIGMA: Single-cell tissue-specific gene prioritization using machine learning
Saranya Balachandran, Cesar A Prada-Medina, Martin A Mensah, et al.
Human Genetics
|
December 21, 2024
Further evidence of biallelic NAV3 variants associated with recessive neurodevelopmental disorder with dysmorphism, developmental delay, intellectual disability, and behavioral abnormalities
Naseebullah Kakar, Selinda Mascarenhas, Asmat Ali, et al.
Brain : a Journal of Neurology
|
December 17, 2021
Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state
Semra Smajić, Cesar A Prada-Medina, Zied Landoulsi, et al.
American Journal of Human Genetics
|
June 4, 2026
HiFi sequencing accurately identifies clinically relevant variants in paralogous genes
Bart van der Sanden, Christian Betz, Katharina Herzog, et al.
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Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Journal of Medical Genetics
|
July 5, 2022
The role of single-cell genomics in human genetics
Varun K A Sreenivasan, Saranya Balachandran, Malte Spielmann
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
November 19, 2022
Comparative single-cell analysis of the adult heart and coronary vasculature
Saranya Balachandran, Jelena Pozojevic, Varun K A Sreenivasan, et al.
Viruses
|
January 22, 2022
Non-Random Pattern of Integration for Epstein-Barr Virus with Preference for Gene-Poor Genomic Chromosomal Regions into the Genome of Burkitt Lymphoma Cell Lines
Snjezana Janjetovic, Juliane Hinke, Saranya Balachandran, et al.
Clinical Genetics
|
January 18, 2025
Haplotype Phasing of Biallelic WNT10B Variants Using Long-Read Sequencing in Split-Hand/Foot Malformation Syndrome
Jelena Pozojevic, Naseebullah Kakar, Henrike L Sczakiel, et al.
Development (Cambridge, England)
|
January 30, 2023
Single-cell RNA-based phenotyping reveals a pivotal role of thyroid hormone receptor alpha for hypothalamic development
Varun K A Sreenivasan, Riccardo Dore, Julia Resch, et al.
American Journal of Human Genetics
|
January 16, 2024
STIGMA: Single-cell tissue-specific gene prioritization using machine learning
Saranya Balachandran, Cesar A Prada-Medina, Martin A Mensah, et al.
American Journal of Human Genetics
|
March 8, 2024
STIGMA: Single-cell tissue-specific gene prioritization using machine learning
Saranya Balachandran, Cesar A Prada-Medina, Martin A Mensah, et al.
Human Genetics
|
December 21, 2024
Further evidence of biallelic NAV3 variants associated with recessive neurodevelopmental disorder with dysmorphism, developmental delay, intellectual disability, and behavioral abnormalities
Naseebullah Kakar, Selinda Mascarenhas, Asmat Ali, et al.
Brain : a Journal of Neurology
|
December 17, 2021
Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state
Semra Smajić, Cesar A Prada-Medina, Zied Landoulsi, et al.
American Journal of Human Genetics
|
June 4, 2026
HiFi sequencing accurately identifies clinically relevant variants in paralogous genes
Bart van der Sanden, Christian Betz, Katharina Herzog, et al.
Page
of 2