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Role of ARHGAP29 nucleotide variants in the etiology of non-syndromic cleft lip with or without cleft palate

Journal of medical science, 2020-06, Vol.89 (2), p.e414

2020

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Whole exome sequencing in recurrent early pregnancy loss

Molecular human reproduction, 2016-05, Vol.22 (5), p.364-372

2016

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Genetic analysis and allele-specific expression of SMAD7 3′UTR variants in human colorectal cancer reveal a novel somatic variant exhibiting allelic imbalance

Gene, 2023-04, Vol.859, p.147217, Article 147217

2023

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A Comprehensive Survey of Genomic Mutations in Breast Cancer Reveals Recurrent Neoantigens as Potential Therapeutic Targets

Frontiers in oncology, 2022-03, Vol.12, p.786438-786438

2022

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Mitochondrial genome variants associated with amyotrophic lateral sclerosis and their haplogroup distribution

Muscle & nerve, 2024-10, Vol.70 (4), p.862-872

2024

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Rescue of Senecavirus A to uncover mutation profiles of its progenies during 80 serial passages in vitro

Veterinary microbiology, 2021-02, Vol.253, p.108969-108969, Article 108969

2021

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Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection

Current Protocols in Bioinformatics, 2013-12, Vol.44 (1), p.15.4.1-15.4.17

2013

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Genetics of Schizophrenia: Overview of Methods, Findings and Limitations

Frontiers in human neuroscience, 2017-06, Vol.11, p.322-322

2017

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CRISPR-Mediated Base Editing: Promises and Challenges for a Viable Oncotherapy Strategy

Human gene therapy, 2023-08, Vol.34 (15-16), p.669-681

2023

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Analysis of Doberman Pinscher and Toy Poodle samples with targeted next-generation sequencing

Gene, 2023-02, Vol.853, p.147069-147069, Article 147069

2023

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Application of next-generation sequencing to characterize novel mutations in clarithromycin-susceptible Helicobacter pylori strains with A2143G of 23S rRNA gene

Annals of clinical microbiology and antimicrobials, 2018-03, Vol.17 (1), p.10-10, Article 10

2018

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microRNAs deregulation in head and neck squamous cell carcinoma

Head & neck, 2021-02, Vol.43 (2), p.645-667

2021

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Selected cachaça yeast strains share a genomic profile related to traits relevant to industrial fermentation processes

Applied and environmental microbiology, 2024-01, Vol.90 (1), p.e0175923

2024

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Unveiling the genetic symphony: Diversity and expression of chicken IFITM genes in Aseel and Kadaknath breeds

Heliyon, 2024-09, Vol.10 (18), p.e37729, Article e37729

2024

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Genetic characteristics involved in COVID‐19 severity. The CARGENCORS case‐control study and meta‐analysis

Journal of medical virology, 2024-02, Vol.96 (2), p.e29404-n/a

2024

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Origins and characterization of variants shared between databases of somatic and germline human mutations

BMC bioinformatics, 2020-06, Vol.21 (1), p.1-227, Article 227

2020

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An in-silico study to determine susceptibility to cancer by evaluating the coding and non-coding non-synonymous single nucleotide variants in the SOCS3 gene

Journal of biomolecular structure & dynamics, 2024-11, Vol.42 (16), p.8281-8292

2024

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MRAS in coronary artery disease—Unchartered territory

IUBMB life, 2024-06, Vol.76 (6), p.300-312

2024

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Two single nucleotide variants in the miR‐23a promoter affect granulosa cell apoptosis

Animal genetics, 2023-04, Vol.54 (2), p.207-210

2023

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Blood Phytosterol Concentration and Genetic Variant Associations in a Sample Population

Nutrients, 2024-04, Vol.16 (7), p.1067

2024

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FiNGS: high quality somatic mutations using filters for next generation sequencing

BMC bioinformatics, 2021-02, Vol.22 (1), p.77-77, Article 77

2021

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Influence of Genetic Variations in miRNA and Genes Encoding Proteins in the miRNA Synthesis Complex on Toxicity of the Treatment of Pediatric B-Cell ALL in the Brazilian Amazon

International journal of molecular sciences, 2023-02, Vol.24 (5), p.4431

2023

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Meta‐analysis of massively parallel reporter assays enables prediction of regulatory function across cell types

Human mutation, 2019-09, Vol.40 (9), p.1299-1313

2019

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Human ACE2 Genetic Polymorphism Affecting SARS-CoV and SARS-CoV-2 Entry into Cells

Microbiology spectrum, 2022-07, Vol.10 (4)

2022

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Role of ARHGAP29 nucleotide variants in the etiology of non-syndromic cleft lip with or without cleft palate

Whole exome sequencing in recurrent early pregnancy loss

Genetic analysis and allele-specific expression of SMAD7 3′UTR variants in human colorectal cancer reveal a novel somatic variant exhibiting allelic imbalance

A Comprehensive Survey of Genomic Mutations in Breast Cancer Reveals Recurrent Neoantigens as Potential Therapeutic Targets

Mitochondrial genome variants associated with amyotrophic lateral sclerosis and their haplogroup distribution

Rescue of Senecavirus A to uncover mutation profiles of its progenies during 80 serial passages in vitro

Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection

Genetics of Schizophrenia: Overview of Methods, Findings and Limitations

CRISPR-Mediated Base Editing: Promises and Challenges for a Viable Oncotherapy Strategy

Analysis of Doberman Pinscher and Toy Poodle samples with targeted next-generation sequencing

Application of next-generation sequencing to characterize novel mutations in clarithromycin-susceptible Helicobacter pylori strains with A2143G of 23S rRNA gene

microRNAs deregulation in head and neck squamous cell carcinoma

Selected cachaça yeast strains share a genomic profile related to traits relevant to industrial fermentation processes

Unveiling the genetic symphony: Diversity and expression of chicken IFITM genes in Aseel and Kadaknath breeds

Genetic characteristics involved in COVID‐19 severity. The CARGENCORS case‐control study and meta‐analysis

Origins and characterization of variants shared between databases of somatic and germline human mutations

An in-silico study to determine susceptibility to cancer by evaluating the coding and non-coding non-synonymous single nucleotide variants in the SOCS3 gene

MRAS in coronary artery disease—Unchartered territory

Two single nucleotide variants in the miR‐23a promoter affect granulosa cell apoptosis

Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study

Blood Phytosterol Concentration and Genetic Variant Associations in a Sample Population

FiNGS: high quality somatic mutations using filters for next generation sequencing

Influence of Genetic Variations in miRNA and Genes Encoding Proteins in the miRNA Synthesis Complex on Toxicity of the Treatment of Pediatric B-Cell ALL in the Brazilian Amazon

Meta‐analysis of massively parallel reporter assays enables prediction of regulatory function across cell types

Human ACE2 Genetic Polymorphism Affecting SARS-CoV and SARS-CoV-2 Entry into Cells

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