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Sergey Oreshkov

Showing results (1-10 of 11) with videos related to

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Bioinformatics (Oxford, England)|August 11, 2024
pyTWMR: transcriptome-wide Mendelian randomization in pythonSergey 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 SequencingAinee Zafar, Ruqia Mehmood Baig, Abida Arshad, et al.
Genome Biology|October 14, 2024
When less is more: sketching with minimizers in genomicsMalick 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 reportMaxime 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 FamiliesRazia 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 positiveZoë 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 familyAsad 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 familyAsad 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 patientsSaba Bibi, Asad Munir, Fawad Ali, et al.
Retrovirology|June 17, 2026
Genetic and transcriptomic signatures of host control in HIV-1 infectionSergey Oreshkov, Christian W Thorball, Jenny Meylan, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|August 11, 2024
pyTWMR: transcriptome-wide Mendelian randomization in pythonSergey 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 SequencingAinee Zafar, Ruqia Mehmood Baig, Abida Arshad, et al.
Genome Biology|October 14, 2024
When less is more: sketching with minimizers in genomicsMalick 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 reportMaxime 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 FamiliesRazia 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 positiveZoë 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 familyAsad 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 familyAsad 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 patientsSaba Bibi, Asad Munir, Fawad Ali, et al.
Retrovirology|June 17, 2026
Genetic and transcriptomic signatures of host control in HIV-1 infectionSergey Oreshkov, Christian W Thorball, Jenny Meylan, et al.
Pageof 2