1,338,924 results match your criteria: "Genetic Variation"

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Embryonic and postembryonic development of the ornamental twin-tail goldfish.
Ing-Jia Li, Shu-Hua Lee, Gembu Abe, Kinya G Ota

April 2019

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Genetics of attention deficit hyperactivity disorder.
Stephen V Faraone, Henrik Larsson

Mol Psychiatry· April 2019

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Origin and evolution of pathogenic coronaviruses.
Jie Cui, Fang Li, Zheng-Li Shi

Nat Rev Microbiol· March 2019

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Genetic analysis of a major international collection of cultivated apple varieties reveals previously unknown historic heteroploid and inbred relationships.
Matthew Ordidge, Pianpool Kirdwichai, M Fazil Baksh, Edward P Venison, J George Gibbings

February 2019

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Neuropeptides as facilitators of domestication.
Yury E Herbeck, Rimma G Gulevich

Cell Tissue Res· January 2019

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Genetic architecture of human thinness compared to severe obesity.
Fernando Riveros-McKay, Vanisha Mistry, Rebecca Bounds, Audrey Hendricks, Julia M Keogh

PLoS Genet· January 2019

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Effects of Common CYP1A2 Genotypes and Other Key Factors on Intraindividual Variation in the Caffeine Metabolic Ratio: An Exploratory Analysis.
Dan-Dan Tian, Senthil Natesan, John R White, Mary F Paine

Clin Transl Sci· January 2019

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encephalopathy: A distinctive generalized developmental and epileptic encephalopathy.
Danique R M Vlaskamp, Benjamin J Shaw, Rosemary Burgess, Davide Mei, Martino Montomoli

Neurology· January 2019

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Association of Triglyceride-Lowering LPL Variants and LDL-C-Lowering LDLR Variants With Risk of Coronary Heart Disease.
Brian A Ference, John J P Kastelein, Kausik K Ray, Henry N Ginsberg, M John Chapman

JAMA· January 2019

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Early human dispersals within the Americas.
J Víctor Moreno-Mayar, Lasse Vinner, Peter de Barros Damgaard, Constanza de la Fuente, Jeffrey Chan

December 2018

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The myostatin gene: an overview of mechanisms of action and its relevance to livestock animals.
D Aiello, K Patel, E Lasagna

Anim Genet· December 2018

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Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability.
Michael D Morgan, Erola Pairo-Castineira, Konrad Rawlik, Oriol Canela-Xandri, Jonathan Rees

Nat Commun· December 2018

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Ten things you should know about transposable elements.
Guillaume Bourque, Kathleen H Burns, Mary Gehring, Vera Gorbunova, Andrei Seluanov

Genome Biol· November 2018

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Bakery yeasts, a new model for studies in ecology and evolution.
Belén Carbonetto, Johan Ramsayer, Thibault Nidelet, Judith Legrand, Delphine Sicard

Yeast· November 2018

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Somatic mutant clones colonize the human esophagus with age.
Iñigo Martincorena, Joanna C Fowler, Agnieszka Wabik, Andrew R J Lawson, Federico Abascal

Science· November 2018

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High throughput ANI analysis of 90K prokaryotic genomes reveals clear species boundaries.
Chirag Jain, Luis M Rodriguez-R, Adam M Phillippy, Konstantinos T Konstantinidis, Srinivas Aluru

Nat Commun· November 2018

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Oldest skeleton of a fossil flying squirrel casts new light on the phylogeny of the group.
Isaac Casanovas-Vilar, Joan Garcia-Porta, Josep Fortuny, Óscar Sanisidro, Jérôme Prieto

Elife· October 2018

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Chromosome evolution at the origin of the ancestral vertebrate genome.
Christine Sacerdot, Alexandra Louis, Céline Bon, Camille Berthelot, Hugues Roest Crollius

Genome Biol· October 2018

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Genomic history of the Sardinian population.
Charleston W K Chiang, Joseph H Marcus, Carlo Sidore, Arjun Biddanda, Hussein Al-Asadi

Nat Genet· October 2018

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A Mendelian randomization study of the effects of blood lipids on breast cancer risk.
Christoph Nowak, Johan Ärnlöv

September 2018

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Impact of Lipids on Cardiovascular Health: JACC Health Promotion Series.
Brian A Ference, Ian Graham, Lale Tokgozoglu, Alberico L Catapano

J Am Coll Cardiol· September 2018

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Blood-based tumor mutational burden as a predictor of clinical benefit in non-small-cell lung cancer patients treated with atezolizumab.
David R Gandara, Sarah M Paul, Marcin Kowanetz, Erica Schleifman, Wei Zou

September 2018

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Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations.
Kristiina Tambets, Bayazit Yunusbayev, Georgi Hudjashov, Anne-Mai Ilumäe, Siiri Rootsi

Genome Biol· September 2018

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Caffeine, CYP1A2 Genotype, and Endurance Performance in Athletes.
Nanci Guest, Paul Corey, Jason Vescovi, Ahmed El-Sohemy

Med Sci Sports Exerc· August 2018

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A Zombie LIF Gene in Elephants Is Upregulated by TP53 to Induce Apoptosis in Response to DNA Damage.
Juan Manuel Vazquez, Michael Sulak, Sravanthi Chigurupati, Vincent J Lynch

August 2018

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Association of Coffee Drinking With Mortality by Genetic Variation in Caffeine Metabolism: Findings From the UK Biobank.
Erikka Loftfield, Marilyn C Cornelis, Neil Caporaso, Kai Yu, Rashmi Sinha

JAMA Intern Med· August 2018

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Fetal microchimerism in human brain tumors.
Lauren Broestl, Joshua B Rubin, Sonika Dahiya

July 2018

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High Diversity and Genetic Variability of Andean Weevil Populations (Premnotrypes vorax, Curculionidae) from the Amazonas Region on the Basis of Mitochondrial DNA Data.
Evelyn V Portocarrero, Martha S Calderon, Danilo E Bustamante

Neotrop Entomol· December 2025

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Combining re-evaluation and new exome sequencing to identify novel genetic variants and candidate genes in Iranian families with non-syndromic hearing loss.
Raziye Rezvani Rezvandeh, Negar Kazemi, Farzane Zare Ashrafi, Ebrahim Shokouhian, Zahra Bolghanabadi

Mol Biol Rep· December 2025

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Association of CYP3A4*1B and SLC6A11 Genetic Variants with Epilepsy Risk And Antiepileptic Drug Response in an Iraqi Population.
Wisam Hindawi Hoidy, Mohammed Hamza Al-Saadi

Mol Neurobiol· December 2025

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CARD9 Mutations in Patients with Invasive Fungal Infections.
Gizem Guner Ozenen, Enise Avci Durmusalioglu, Durdugul Ayyildiz Emecen, Nimet Melis Bilen, Zuhal Umit

Mycopathologia· December 2025

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Association between deletions in the preS1/2 region of the hepatitis B virus genome and persistently abnormal ALT levels in patients with chronic hepatitis B treated with nucleos(t)ide analogs.
Yurina Sato, Kotaro Doi, Jun Inoue, Masashi Ninomiya, Mio Tsuruoka

Arch Virol· December 2025

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Distinct impact of RNF213 p.R4810K genotype on transdural collateral formation across Japanese Asian and Polish Caucasian Moyamoya patients.
Dariusz Szarek, Masaki Ito, Haruto Uchino, Katarzyna Lubkowska, Kikutaro Tokairin

Neurosurg Rev· December 2025

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Phenotypic effect of the mutations H78Y and L83V in the E6 protein of human papillomavirus.
N Di Domizio, A Debernardi, M Olivier, E Bôle-Richard, B Caël

Arch Virol· December 2025

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Preclinical evaluation of [C]CHDI-009R for quantification of mutant huntingtin aggregates.
Franziska Zajicek, Liesbeth Everix, Annemie Van Eetveldt, Jeroen Verhaeghe, Stef De Lombaerde

J Mol Med (Berl)· December 2025

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Convergent mutation trajectories convert functional self-tolerance in IGHV4-34 B cells to genetic tolerance encoded in the antibody.
Christopher J Jara, Sherin Zachariah, Katherine J L Jackson, Timothy J Peters, Etienne Masle-Farquhar

Proc Natl Acad Sci U S A· December 2025

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Interprotomer communication and functional asymmetry in H/ACA snoRNPs.
Hemendra Singh Panwar, Timothy J Vos, Xiaoyan Xie, H Josh Jang, Hyoungjoo Lee

Proc Natl Acad Sci U S A· December 2025

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Identification of HLA class II-restricted T cell receptors against shared PIK3CA mutations in patients with epithelial cancers.
S M Rafiqul Islam, Samantha Seitter, Maria Parkhurst, Frank J Lowery, Miaki Fukuhara

Cancer Immunol Immunother· December 2025

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Unveiling the genomic and phenotypic landscape of Acinetobacter species from different environmental sources in Brazil.
Amanda Yaeko Yamada, Anna Luiza Bauer Canellas, Matheus Nunes Diniz, Pedro Smith Pereira Ferraro, Daniel de Sena Miranda

Antonie Van Leeuwenhoek· December 2025

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SynSeg: A synthetic data-driven approach for robust subcellular structure segmentation.
Zhengyang Guo, Zi Wang, Zihan Chen, Kaiming Xu, Yongping Chai

J Cell Biol· March 2026

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Molecular drivers of osteogenesis imperfecta: a cellular and extracellular collagen disease.
Silvia Cotti, Wendy Pérez Franco, Antonella Forlino

Clin Sci (Lond)· December 2025

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Environmental surveillance reveals enterovirus diversity in Jinan, China: detection of types D68, A71, A76, B88, A90, and C99.
Mengmeng Wang, Feng Ji, Meng Chen, Yao Liu, Xiaojuan Lin

Microbiol Spectr· December 2025

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The tomato seed microbiome is mainly shaped by host genotype and production site.
Xiaoyulong Chen, Expedito Olimi, Carolina Lobato, Gabriele Berg, Tomislav Cernava

mSystems· December 2025

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and polymorphisms exhibit distinct association patterns in active and latent tuberculosis.
Ezza Binte Tariq, Urooj Subhan, Farah Deeba, Zuha Tariq, Afrose Liaquat

J Med Microbiol· December 2025

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Bradycardia in Athletes: Prevalence, Mechanisms, and Risks.
Paolo D'Ambrosio, Jarne De Paepe, Luke W Spencer, Monique Ohanian, Kristel Janssens

Circulation· December 2025

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A New Allele HLA-DQB1*06:02:01:42 Identified by HLA-Targeted Third-Generation Sequencing in a Chinese Individual.
Jindou Wang, Guiliang Shen, Xinyu Wang, Peng Gao, Yuanli Zhao

HLA· December 2025

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Two GWAS Suggestive-SNVs in the Zinc Transporter 8 Gene Synergistically Influence Insulin Resistance in Type 2 Diabetes.
Abdolkarim Mahrooz, Mina Safari, Mani Nosrati, Mehran Ahmadi, Ahad Alizadeh

Int J Prev Med· December 2025

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Sex-Specific Genetic Architecture and Comorbidities of Alcohol Use Behaviors.
Laura Vilar-Ribó, Mariela V Jennings, Aisha Sallah, Zeal Jinwala, Hayley Ha Thorpe

medRxiv· December 2025

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Nomogram model based on ultrasonography and contrast-enhanced CT for predicting BRAF mutation in thyroid nodules classified as C-TIRADS 3 and above.
Wenran Zhang, Chenfan Yu, Yu Gao, Jiaqing Dou

Front Endocrinol (Lausanne)· December 2025

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StarTRAC-: a method for allele-specific copy number determination using digital PCR.
Wendy Y Wang, Erin C Boone, Lancy Lin, David Joun, Andrea Gaedigk

Front Pharmacol· December 2025

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Double Genetic Diagnosis Involving MECP2 and EPHB4 in a Child with Neurodevelopmental Delay and Vascular Anomalies: A Case Report.
Aslihan Sanri, Mehmet Burak Mutlu

Mol Syndromol· October 2025

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Two Unrelated Witteveen-Kolk Syndrome Patients Presenting with Unusual Clinical Features: Dual Diagnosis and Atypical Rare Manifestation.
Mustafa Yilmaz, Ayse Ozden, Hakan Doneray, Oguzhan Bahadır, Tuna Apuhan

Mol Syndromol· November 2025

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A Novel Frameshift Variant Presenting with Autism and Psychiatric Features: Intrafamilial Phenotypic Variation - A Case Report.
Sermin Özcan, Burcu Yeter

Mol Syndromol· October 2025

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VEXAS syndrome in rheumatology practice: features from a multicenter cohort in north-east Italy.
Sara Bindoli, Greta Morello-Pasin, Irina Guidea, Roberto Padoan, Luca Iorio

Front Immunol· December 2025

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