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Why, When and How to Adjust Your P Values?

Cell journal (Yakhteh), 2019, Vol.20 (4), p.604-607

2019

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Whole-genome analysis of Nigerian patients with breast cancer reveals ethnic-driven somatic evolution and distinct genomic subtypes

Nature communications, 2021-11, Vol.12 (1), p.6946-6946, Article 6946

2021

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Multi-site clonality analysis uncovers pervasive heterogeneity across melanoma metastases

Nature communications, 2020-08, Vol.11 (1), p.4306-4306, Article 4306

2020

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Association of MSY haplotype background with nonobstructive azoospermia is AZF‐dependent: A case‐control study

Andrologia, 2021-03, Vol.53 (2), p.e13946-n/a

2021

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Identification of a missense variant in CLDN2 in obstructive azoospermia

Journal of human genetics, 2019-10, Vol.64 (10), p.1023-1032

2019

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Re-evaluating experimental validation in the Big Data Era: a conceptual argument

Genome Biology, 2021-02, Vol.22 (1), p.71-71, Article 71

2021

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A logic-based dynamic modeling approach to explicate the evolution of the central dogma of molecular biology

PloS one, 2017-12, Vol.12 (12), p.e0189922

2017

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The Essentiality of Reporting Hardy-Weinberg Equilibrium Calculations in Population-Based Genetic Association Studies

Cell journal (Yakhteh), 2015-07, Vol.17 (2), p.187-192

2015

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Little genetic differentiation as assessed by uniparental markers in the presence of substantial language variation in peoples of the Cross River region of Nigeria

BMC evolutionary biology, 2010-03, Vol.10, p.92

2010

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Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

Nature (London), 2013-01, Vol.493 (7432), p.406-410

2013

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Group-based pharmacogenetic prediction: is it feasible and do current NHS England ethnic classifications provide appropriate data?

The pharmacogenomics journal, 2021-02, Vol.21 (1), p.47-59

2021

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Clonal diversification and histogenesis of malignant germ cell tumours

Nature communications, 2022-08, Vol.13 (1), p.4272-4272, Article 4272

2022

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Evidence from Y-chromosome analysis for a late exclusively eastern expansion of the Bantu-speaking people

European journal of human genetics : EJHG, 2013-04, Vol.21 (4), p.423-429

2013

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Cancer origin tracing and timing in two high-risk prostate cancers using multisample whole genome analysis: prospects for personalized medicine

Genome medicine, 2023-10, Vol.15 (1), p.82-82, Article 82

2023

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Can We Assume the Gene Expression Profile as a Proxy for Signaling Network Activity?

Biomolecules (Basel, Switzerland), 2020-06, Vol.10 (6), p.850

2020

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Systems Biomedicine of Rabies Delineates the Affected Signaling Pathways

Frontiers in microbiology, 2016-11, Vol.7, p.1688-1688

2016

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Optimization of Porous Silicon Conditions for DNA-based Biosensing via Reflectometric Interference Spectroscopy

Cell journal (Yakhteh), 2019, Vol.20 (4), p.584-591

2019

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In silico engineering a CD80 variant with increased affinity to CTLA-4 and decreased affinity to CD28 for optimized cancer immunotherapy

Journal of immunological methods, 2023-02, Vol.513, p.113425, Article 113425

2023

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Systems genetics of nonsyndromic orofacial clefting provides insights into its complex aetiology

European journal of human genetics : EJHG, 2019-02, Vol.27 (2), p.226-234

2019

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Multiple cereblon genetic changes are associated with acquired resistance to lenalidomide or pomalidomide in multiple myeloma

Blood, 2021-01, Vol.137 (2), p.232-237

2021

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Testis-Specific Y‑Centric Protein–Protein Interaction Network Provides Clues to the Etiology of Severe Spermatogenic Failure

Journal of proteome research, 2016-03, Vol.15 (3), p.1011-1022

2016

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Genomic Panorama and Clonal Evolutionary Trajectory of Classical Hairy Cell Leukemia

Blood, 2022-11, Vol.140 (Supplement 1), p.8748-8749

2022

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Genomic and evolutionary classification of lung cancer in never smokers

Nature genetics, 2021-09, Vol.53 (9), p.1348-1359

2021

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Label-free discrimination of single nucleotide changes in DNA by reflectometric interference Fourier transform spectroscopy

Colloids and surfaces, B, Biointerfaces, 2019-09, Vol.181, p.714-720

2019

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Whole-genome analysis identifies novel drivers and high-risk double-hit events in relapsed/refractory myeloma

Blood, 2023-02, Vol.141 (6), p.620-633

2023

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Why, When and How to Adjust Your P Values?

Whole-genome analysis of Nigerian patients with breast cancer reveals ethnic-driven somatic evolution and distinct genomic subtypes

Multi-site clonality analysis uncovers pervasive heterogeneity across melanoma metastases

Association of MSY haplotype background with nonobstructive azoospermia is AZF‐dependent: A case‐control study

Identification of a missense variant in CLDN2 in obstructive azoospermia

Re-evaluating experimental validation in the Big Data Era: a conceptual argument

A logic-based dynamic modeling approach to explicate the evolution of the central dogma of molecular biology

The Essentiality of Reporting Hardy-Weinberg Equilibrium Calculations in Population-Based Genetic Association Studies

Little genetic differentiation as assessed by uniparental markers in the presence of substantial language variation in peoples of the Cross River region of Nigeria

Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

Group-based pharmacogenetic prediction: is it feasible and do current NHS England ethnic classifications provide appropriate data?

Clonal diversification and histogenesis of malignant germ cell tumours

Evidence from Y-chromosome analysis for a late exclusively eastern expansion of the Bantu-speaking people

Cancer origin tracing and timing in two high-risk prostate cancers using multisample whole genome analysis: prospects for personalized medicine

Can We Assume the Gene Expression Profile as a Proxy for Signaling Network Activity?

Systems Biomedicine of Rabies Delineates the Affected Signaling Pathways

Optimization of Porous Silicon Conditions for DNA-based Biosensing via Reflectometric Interference Spectroscopy

In silico engineering a CD80 variant with increased affinity to CTLA-4 and decreased affinity to CD28 for optimized cancer immunotherapy

Systems genetics of nonsyndromic orofacial clefting provides insights into its complex aetiology

Multiple cereblon genetic changes are associated with acquired resistance to lenalidomide or pomalidomide in multiple myeloma

Testis-Specific Y‑Centric Protein–Protein Interaction Network Provides Clues to the Etiology of Severe Spermatogenic Failure

Genomic Panorama and Clonal Evolutionary Trajectory of Classical Hairy Cell Leukemia

Genomic and evolutionary classification of lung cancer in never smokers

Label-free discrimination of single nucleotide changes in DNA by reflectometric interference Fourier transform spectroscopy

Whole-genome analysis identifies novel drivers and high-risk double-hit events in relapsed/refractory myeloma

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