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Bioinformatics (Oxford, England)
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August 11, 2024
pyTWMR: transcriptome-wide Mendelian randomization in python
Sergey Oreshkov, Kaido Lepik, Federico Santoni
International Journal of Molecular Sciences
|
March 27, 2025
Deciphering the Genetic Basis of Degenerative and Developmental Eye Disorders in 50 Pakistani Consanguineous Families Using Whole-Exome Sequencing
Ainee Zafar, Ruqia Mehmood Baig, Abida Arshad, et al.
Genome Biology
|
October 14, 2024
When less is more: sketching with minimizers in genomics
Malick Ndiaye, Silvia Prieto-Baños, Lucy M Fitzgerald, et al.
BJC Reports
|
June 16, 2025
Whole genome sequencing and single-cell transcriptomics identify KMT2D inactivation as a potential new driver for pituitary tumors: a case report
Maxime Brunner, Jenny Meylan-Merlini, Maude Muriset, et al.
Genes
|
May 27, 2026
Expanding the Genetic Landscape of Congenital Stationary Night Blindness Through the Analysis of Consanguineous Pakistani Families
Razia Parveen, Muhammad Iqbal, Shahbaz Khan, et al.
Mitochondrion
|
November 1, 2023
Reanalysis of mtDNA mutations of human primordial germ cells (PGCs) reveals NUMT contamination and suggests that selection in PGCs may be positive
Zoë Fleischmann, Auden Cote-L'Heureux, Melissa Franco, et al.
Ophthalmic Genetics
|
November 21, 2024
A novel homozygous missense variant in <i>POC1B</i> causes cone dystrophy in a consanguineous Pakistani family
Asad Munir, Inam Ullah Khan, Abdur Rashid, et al.
Human Genome Variation
|
November 18, 2025
A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani family
Asad Munir, Helen Nabiryo Frederiksen, Fawad Ali, et al.
Human Genome Variation
|
April 27, 2026
Duplication of 4-bp in SACS leads to autosomal recessive spastic ataxia of Charlevoix-Saguenay type in two Pakistani patients
Saba Bibi, Asad Munir, Fawad Ali, et al.
Retrovirology
|
June 17, 2026
Genetic and transcriptomic signatures of host control in HIV-1 infection
Sergey Oreshkov, Christian W Thorball, Jenny Meylan, et al.
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Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Bioinformatics (Oxford, England)
|
August 11, 2024
pyTWMR: transcriptome-wide Mendelian randomization in python
Sergey Oreshkov, Kaido Lepik, Federico Santoni
International Journal of Molecular Sciences
|
March 27, 2025
Deciphering the Genetic Basis of Degenerative and Developmental Eye Disorders in 50 Pakistani Consanguineous Families Using Whole-Exome Sequencing
Ainee Zafar, Ruqia Mehmood Baig, Abida Arshad, et al.
Genome Biology
|
October 14, 2024
When less is more: sketching with minimizers in genomics
Malick Ndiaye, Silvia Prieto-Baños, Lucy M Fitzgerald, et al.
BJC Reports
|
June 16, 2025
Whole genome sequencing and single-cell transcriptomics identify KMT2D inactivation as a potential new driver for pituitary tumors: a case report
Maxime Brunner, Jenny Meylan-Merlini, Maude Muriset, et al.
Genes
|
May 27, 2026
Expanding the Genetic Landscape of Congenital Stationary Night Blindness Through the Analysis of Consanguineous Pakistani Families
Razia Parveen, Muhammad Iqbal, Shahbaz Khan, et al.
Mitochondrion
|
November 1, 2023
Reanalysis of mtDNA mutations of human primordial germ cells (PGCs) reveals NUMT contamination and suggests that selection in PGCs may be positive
Zoë Fleischmann, Auden Cote-L'Heureux, Melissa Franco, et al.
Ophthalmic Genetics
|
November 21, 2024
A novel homozygous missense variant in <i>POC1B</i> causes cone dystrophy in a consanguineous Pakistani family
Asad Munir, Inam Ullah Khan, Abdur Rashid, et al.
Human Genome Variation
|
November 18, 2025
A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani family
Asad Munir, Helen Nabiryo Frederiksen, Fawad Ali, et al.
Human Genome Variation
|
April 27, 2026
Duplication of 4-bp in SACS leads to autosomal recessive spastic ataxia of Charlevoix-Saguenay type in two Pakistani patients
Saba Bibi, Asad Munir, Fawad Ali, et al.
Retrovirology
|
June 17, 2026
Genetic and transcriptomic signatures of host control in HIV-1 infection
Sergey Oreshkov, Christian W Thorball, Jenny Meylan, et al.
Page
of 2