Archived HIV-1 Drug Resistance Mutations: Role of Proviral HIV-1 DNA Genotype for the Management of Virological Responder People Living with HIV.
Viruses | 2024-10-30 | PMID 39599811
Campagna Roberta, Nonne Chiara, Antonelli Guido and 1 more
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
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Publications
Page 98 of 10600
Linking molecular mechanisms to their evolutionary consequences: a primer.
Genetics | 2025-02-05 | PMID 39601269
Grah Rok, Guet Calin C, Tkačik Gasper and 1 more
Virulence-associated variants in Cryptococcus neoformans sequence type 93 are less likely to be associated with population structure compared to independent rare mutations.
Microbiology spectrum | 2025-01-07 | PMID 39601574
Jackson Katrina M, Kabbale Kisakye Diana, Macchietto Marissa and 3 more
Single nucleotide polymorphisms are associated with strain-specific virulence differences among clinical isolates of Cryptococcus neoformans.
Nature communications | 2024-12-02 | PMID 39622806
Jackson Katrina M, Kono Thomas J Y, Betancourt Jovany J and 14 more
Rapid Adaption but Genetic Diversity Loss of a Globally Distributed Diatom in the Warmer Ocean.
Global change biology | 2024-12-01 | PMID 39629602
Cheng Luman, Xu Xiuming, Wang Minghua and 1 more
Genetic variant in the AGT gene (rs699-GG) is associated with severe COVID-19 in Brazilian patients.
Anais da Academia Brasileira de Ciencias | 2024-01-01 | PMID 39630802
Farias Pablo C S, Cabral Leandro P, Neves Patrícia A F and 9 more
Correlation between the APOE ε4 genotype, lifestyle habits, and cognitive deficits in Chinese adults over 60: a cross-sectional analysis in China.
Frontiers in public health | 2024-01-01 | PMID 39639910
Li Wei, Wang XiaoLiang, Sun Lin and 2 more
Synthetic mismatches enable specific CRISPR-Cas12a-based detection of genome-wide SNVs tracked by ARTEMIS.
Cell reports methods | 2024-12-16 | PMID 39644903
Kohabir Kavish A V, Linthorst Jasper, Nooi Lars O and 3 more
Characterization of Newly Isolated Bacteriophages Targeting Carbapenem-Resistant Klebsiella pneumoniae.
Journal of microbiology (Seoul, Korea) | 2024-12-01 | PMID 39656423
Kim Bokyung, Kim Shukho, Choi Yoon-Jung and 2 more
Extending evolutionary forecasts across bacterial species.
Proceedings. Biological sciences | 2024-12-01 | PMID 39657800
Pentz Jennifer T, Biswas Aparna, Alsaed Bassel and 1 more
Concordance analysis between Human Papillomavirus genotyping assay and PCR-reverse spot hybridization for the detection of Human Papillomavirus infection.
Journal of medical microbiology | 2024-12-01 | PMID 39670833
Chen Yanlin, Li Ye, Xue Lifang and 4 more
Genetic profile in primary tumor tissue of advanced lung adenocarcinoma patients with adrenal metastasis.
Cancer genetics | 2025-01-01 | PMID 39673828
Pan Haiqiao, Zhang Hongbin, Zhang Yongqian and 7 more
Genes: EGFR, KRAS, ALK, TNF, KEAP1, LRP1B, NOTCH1, RET
Exploring phenotypes to improve long-term mortality risk stratification in obstructive sleep apnea through a machine learning approach: an observational cohort study.
European journal of internal medicine | 2025-03-01 | PMID 39690003
Tondo Pasquale, Scioscia Giulia, Bailly Sebastien and 7 more
Genes: CPAP
Isolated Langerhans cell histiocytosis of the stomach in adults: An analysis of clinicopathologic characteristics and molecular genetics.
Medicine | 2024-12-20 | PMID 39705477
Wu Ruinuan, Zhao Yali, Wu Xikang and 3 more
The role of inflammatory gene polymorphisms in severe COVID-19: a review.
Virology journal | 2024-12-20 | PMID 39707400
Yip Jia Qi, Oo Adrian, Ng Yan Ling and 5 more
Mutability and hypermutation antagonize immunoglobulin codon optimality.
Molecular cell | 2025-01-16 | PMID 39708804
McGrath Joshua J C, Park Juyeon, Troxell Chloe A and 14 more
Genes: IGH
Beyond BRAFV600E: Investigating the Clinical and Genetic Spectrum of Langerhans Cell Histiocytosis in Children.
Cancer medicine | 2024-12-01 | PMID 39711503
Tang Xue, Gao Ju, Guo Xia and 2 more
Case-control association study between polygenic risk score and COVID-19 severity in a Russian population using low-pass genome sequencing.
Epidemiology and infection | 2024-12-26 | PMID 39721951
Nostaeva Arina, Shimansky Valentin, Apalko Svetlana and 9 more
MOLECULAR-GENETIC PHENOTYPES OF BREAST CANCER, THEIR PROLIFERATIVE ACTIVITY, DEGREE OF SPREADING AND DIFFERENTIATION IN PATIENTS WHICH WERE SUFFERED BY THE ACCIDENT AT ChNPP.
Problemy radiatsiinoi medytsyny ta radiobiolohii | 2024-12-01 | PMID 39724624
Bazyka D A, Litvinenko O O
Cerebral Cavernous Malformation: From Genetics to Pharmacotherapy.
Brain and behavior | 2025-01-01 | PMID 39740786
Zhang Zhuangzhuang, Deng Jianwen, Sun Weiping and 1 more
Feasibility and Acceptability of Collecting Passive Smartphone Data for Potential Use in Digital Phenotyping Among Family Caregivers and Patients With Advanced Cancer.
JCO clinical cancer informatics | 2025-01-01 | PMID 39746166
Odom J Nicholas, Lee Kyungmi, Currie Erin R and 11 more
Leveraging haplotype information in heritability estimation and polygenic prediction.
Nature communications | 2025-01-02 | PMID 39747034
Meisner Jonas, Benros Michael Eriksen, Rasmussen Simon
Emergence and clinical challenges of ST11-K64 carbapenem-resistant Klebsiella pneumoniae: molecular insights and implications for antimicrobial resistance and virulence in Southwest China.
BMC infectious diseases | 2025-01-03 | PMID 39754049
Li Linlin, Liang Jiahui, Zhang Huan and 3 more
Mutational and co-mutational landscape of early onset colorectal cancer.
Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals | 2025-02-01 | PMID 39761813
Alshenaifi Jumanah Yousef, Vetere Guglielmo, Maddalena Giulia and 16 more
Genes: BRAF, TP53, APC, CTNNB1, KRAS, NOTCH1, NOTCH3, RB1
Insights on the Genetic and Phenotypic Complexities of Optic Neuropathies.
Genes | 2024-11-29 | PMID 39766826
D'Esposito Fabiana, Zeppieri Marco, Cordeiro Maria Francesca and 6 more
Expanding the Genotypic and Phenotypic Spectrum of OFD1-Related Conditions: Three More Cases.
Genes | 2024-12-20 | PMID 39766900
Kyian Tatiana, Borovikov Artem, Anisimova Inga and 10 more
Inactivation of Lipopolysaccharide-Biosynthesizing Genes Altered Lipids Composition and Intensity in Cronobacter sakazakii.
Pathogens (Basel, Switzerland) | 2024-11-23 | PMID 39770295
Hu Xiaoqing, Yang Xi, Wu Shuyan and 6 more
Epigenetics and individuality: from concepts to causality across timescales.
Nature reviews. Genetics | 2025-06-01 | PMID 39789149
Webster Amy K, Phillips Patrick C
Highly-multiplex detection of plasma cell-free human papillomavirus-16 DNA in oropharyngeal carcinoma.
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology | 2025-02-01 | PMID 39793474
Clark Payton, Karasik Natalya, Campbell Shauna R and 13 more
Evaluation of the Toxicity and Outcomes of the Combination of Midostaurin and CLAG-M in Patients With FLT3-Mutated Acute Myeloid Leukemia (AML): A Multicenter Retrospective Analysis.
The Annals of pharmacotherapy | 2025-08-01 | PMID 39800921
Chen Ashley, Baek Grace, Russell Kathryn and 10 more
Genes: FLT3
Outbreak of carbapenem resistant Klebsiella pneumoniae in a neurorehabilitation unit: Genomic epidemiology reveals complex transmission pattern in a tertiary care hospital.
Journal of global antimicrobial resistance | 2025-03-01 | PMID 39818328
Silvotti Maria Grazia, Scaltriti Erika, Bolzoni Luca and 8 more
A Japanese family of hereditary diffuse gastric cancer with a germline pathogenic variant of CTNN1A detected via comprehensive genome profiling.
Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association | 2025-05-01 | PMID 39838246
Kawakami Takeshi, Matsubayashi Hiroyuki, Kiyozumi Yoshimi and 7 more
Genes: CTNNA1, CDH1
Phenome-wide associations of sleep characteristics in the Human Phenotype Project.
Nature medicine | 2025-03-01 | PMID 39870817
Kohn Sarah, Diament Alon, Godneva Anastasia and 5 more
Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms are associated with major depressive disorder in the Saudi patients attending Erada complex for mental health and Erada services - Jeddah, Saudi Arabia.
Die Pharmazie | 2024-12-30 | PMID 39871098
Bagher A M, Alkhaldi M F, Somaily J A and 5 more
Genes: MTHFR
Utility of Digital Phenotyping Based on Wrist Wearables and Smartphones in Psychosis: Observational Study.
JMIR mHealth and uHealth | 2025-02-05 | PMID 39912304
Yang Zixu, Heaukulani Creighton, Sim Amelia and 11 more
Phenotypes of headache in patients with obstructive sleep apnea.
Scientific reports | 2025-02-08 | PMID 39922920
Tripakornkusol Viriya, Sinsopa Napassorn, Khamsai Sittichai and 1 more
Pathogenic variants in the IFT140 gene and an intriguing clinical presentation in two pediatric patients. Cases report and review of literature.
Ophthalmic genetics | 2025-06-01 | PMID 39927556
Koce Maša, Fakin Ana, Markelj Špela and 5 more
Genes: IFT140
Current Smoker: A Clinical Chronic Obstructive Pulmonary Disease Phenotype Affecting Disease Progression and Response to Therapy.
American journal of respiratory and critical care medicine | 2025-05-01 | PMID 39938077
Celli Bartolome R, Christenson Stephanie A, Rabe Klaus F and 9 more
Complete loss of IFT27 function leads to a phenotypic spectrum of fetal lethal ciliopathy associated with altered ciliogenesis.
European journal of human genetics : EJHG | 2025-03-01 | PMID 39955445
Haïm David, Roux Nathalie, Boutaud Lucile and 10 more
Genes: IFT27
Seasonal variation in the associations between self-reported long-COVID symptoms and IL-6 signalling-related factors (particularly the rs2228145 variant of the IL-6R gene): A clinical study.
Cytokine | 2025-05-01 | PMID 39987891
Rees Katie, Aicheler Rebecca, Butcher Lee and 7 more
Insights into genetic architecture and disease associations of genes associated with different human blood group systems using codon usage bias.
Journal of biomolecular structure & dynamics | 2026-04-01 | PMID 39988946
Kumar Utsang, Singhal Shailja, Khan Azmat Ali and 3 more
Genes: GC
Circadian clock features define novel subtypes among breast cancer cells and shape drug sensitivity.
Molecular systems biology | 2025-04-01 | PMID 39994450
Ector Carolin, Didier Jeff, De Landtsheer Sébastien and 7 more
Mutations in the ilvN gene mitigate growth inhibitory effect of cysteine in Corynebacterium glutamicum.
Applied microbiology and biotechnology | 2025-03-10 | PMID 40063103
Matsuhisa Kazuho, Ogawa Katsuhiro, Komata Kento and 1 more
Prevalence of Human Papillomavirus and Genotype Correlation with Cervical Lesions at the University Teaching Hospital of Kigali.
The American journal of tropical medicine and hygiene | 2025-06-04 | PMID 40132222
Mbabazi Evode, Munyemana Jean Bosco, Mukashema Julienne and 4 more
hTAS2R38 polymorphisms modulate oral microbiota and influence the prevalence and treatment outcome of halitosis.
Microbiome | 2025-03-28 | PMID 40156025
Mei Hongxiang, Qi Cai, Liu Jinchi and 7 more
Amyloid precursor protein and presenilin-1 knock-in immunodeficient mice exhibit intraneuronal Aβ pathology, microgliosis, and extensive neuronal loss.
Alzheimer's & dementia : the journal of the Alzheimer's Association | 2025-04-01 | PMID 40195277
Yeapuri Pravin, Machhi Jatin, Foster Emma G and 11 more
Genes: APP, NOG
Streamline: Retrospective Cohort Study of FMS-Like Tyrosine Kinase 3-Mutated Acute Myeloid Leukemia - Real-World Treatment Patterns and Clinical Outcomes of Patients in First Relapse or Refractory Diagnosis.
Acta haematologica | 2026-01-01 | PMID 40228486
Zeidan Amer M, Yu Rebekah, Wang Yuexi and 8 more
Genes: FLT3
The SWI/SNF PBAF complex facilitates REST occupancy at repressive chromatin.
Molecular cell | 2025-05-01 | PMID 40252649
Grossi Elena, Nguyen Christie B, Carcamo Saul and 10 more
Genes: ARID2, REST
Two novel mutations in TBC1D32 add complexity to the oro-facial-digital syndrome.
Human genomics | 2025-05-03 | PMID 40319332
García-Bohórquez Belén, Marín-Reina Purificación, Aller Elena and 6 more
Genes: TBC1D32
FD and FDP bZIP transcription factors and FT florigen regulate floral development and control homeotic gene expression in Arabidopsis floral meristems.
Development (Cambridge, England) | 2025-05-15 | PMID 40326559
Romera-Branchat Maida, Pocard Chloé, Vincent Coral and 7 more
Computational structure-guided approach to simulate delamanid and pretomanid binding to mycobacterial F420 redox cycling proteins: identification of key determinants of resistance.
Journal of biomolecular structure & dynamics | 2025-11-01 | PMID 40326994
Chakraborty Gourav, Kolpe Mahima Sudhir, Nath I V Ambily and 3 more
Adverse Outcome Pathway-Informed Integrated Testing to Identify Chemicals Causing Genotoxicity Through Oxidative DNA Damage: Case Study on 4-Nitroquinoline 1-Oxide.
Environmental and molecular mutagenesis | 2025-04-01 | PMID 40341686
Huliganga Elizabeth, Cho Eunnara, Swartz Carol D and 5 more
Role of apolipoprotein E (ApoE) ε4 in cognitive impairment after a stroke: a prospective cohort study.
Aging | 2025-05-08 | PMID 40349252
Chen Jia-Hung, Chan Lung, Hong Chien-Tai and 2 more
Using eQTL Mendelian randomization and transcriptomic analysis to identify the relationship between ion channel genes and intracranial aneurysmal subarachnoid hemorrhage.
Medicine | 2025-05-16 | PMID 40388745
Wang Jing, Chen Bowang, Meng Qiang and 2 more
Genes: ANO6, CACNA2D3
Large effect life-history genomic regions are associated with functional morphological traits in Atlantic salmon.
G3 (Bethesda, Md.) | 2025-07-09 | PMID 40408779
Aykanat Tutku, Debes Paul V, Jansouz Shadi and 7 more
Eosinophils in chronic obstructive pulmonary disease.
Therapeutic advances in respiratory disease | 2025-01-01 | PMID 40434001
Vanetti Marco, Visca Dina, Ardesi Francesco and 3 more
LRRK2-mediated mitochondrial dysfunction in Parkinson's disease.
The Biochemical journal | 2025-05-28 | PMID 40440058
Buck Silas A, Sanders Laurie H
The role of multi-organ cancer predisposition genes in the risk of inherited and histologically diverse gastric cancer.
EBioMedicine | 2025-06-01 | PMID 40446793
Guerra Joana, Estrada-Florez Ana P, Lott Paul C and 37 more
Genes: GC, CDH1, CTNNA1, APC, ATM, BRCA1, BRCA2, CHEK2
Functional control of heteromeric Kv2.1/6.4 channels by the voltage sensor domain of the silent Kv6.4 subunit.
The Journal of physiology | 2025-06-01 | PMID 40471226
Tewari Debanjan, Sattler Christian, Benndorf Klaus
Polygenic scores for obstructive sleep apnoea reveal pathways contributing to cardiovascular disease.
EBioMedicine | 2025-07-01 | PMID 40472801
Kurniansyah Nuzulul, Strausz Satu J, Chittoor Geetha and 32 more
Phenotypic landscape of an invasive fungal pathogen reveals its unique biology.
Cell | 2025-07-24 | PMID 40505656
Boucher Michael J, Banerjee Sanjita, Joshi Meenakshi B and 19 more
Radiation-induced cerebral cavernous malformations.
Journal of the neurological sciences | 2025-08-15 | PMID 40516174
Tsutsumi Satoshi, Ogino Ikuko, Sugiyama Natsuki and 3 more
Range-Wide Genomic Analysis Reveals Regional and Meta-Population Dynamics of Decline and Recovery in the Grey Seal.
Molecular ecology | 2025-07-01 | PMID 40536212
McCarthy Morgan L, Cammen Kristina M, Granquist Sandra M and 15 more
Feasibility of Collecting and Linking Digital Phenotyping, Clinical, and Genetics Data for Mental Health Research: Pilot Observational Study.
JMIR formative research | 2025-06-23 | PMID 40548985
Beames Joanne R, Dabash Omar, Spoelma Michael J and 12 more
Sleep apnea among individuals with Alpha-1 antitrypsin deficiency-associated lung disease.
Respiratory medicine | 2025-09-01 | PMID 40550287
Holm Kristen E, Sandhaus Robert A, Allison Sheri and 3 more
The Impact of APOE ε4 on Neuropsychological Test Performance in Hispanics: The Panama Aging Research Initiative - Health Disparities Study.
Dementia and geriatric cognitive disorders | 2026-01-01 | PMID 40551395
Villarreal Alcibiades E, Rangel Giselle A, Tratner Adam E and 6 more
Genes: APOE
Parkinson's disease associated with LRRK2-R1441C mutation: Characterization and comparison with other LRRK2 mutations.
Journal of Parkinson's disease | 2025-08-01 | PMID 40611668
Hadad Rafi, Alcalay Roy N, Senderova Inna and 10 more
Association of platelet ADP receptor variant rs1371097 with inadequate platelet response to aspirin in Indian patients.
Personalized medicine | 2025-10-01 | PMID 40644802
Sundaravadivel Pandarisamy, Christopher Rita, Chandra Sadanandavalli Retnaswami and 1 more
Genes: P2RY1, ITGB3, PEAR1, UGT1A6
Seeing is believing-on the utility of CT in phenotyping chronic obstructive pulmonary disease.
The British journal of radiology | 2026-08-01 | PMID 40650927
Awan Hira A, Chaudhary Muhammad F A, Reinhardt Joseph M
Investigating the Efficacy of the CRISPR/Cas9 Gene-Editing System for Targeting the HBB FSC 36-37 (-T) Mutation Locus in Hematopoietic Stem Cells.
Molecular biotechnology | 2026-04-01 | PMID 40676395
Fereydani Nasim Mayeli, Galehdari Hamid, Hoveizi Elham and 4 more
Genes: HBB
"Genetic diversity of Mycobacterium tuberculosis complex in treatment naive sputum smear positive patients as revealed by spoligotyping and MIRU-VNTR."
Indian journal of medical microbiology | 2025-01-01 | PMID 40684880
Srikar Anagoni, Ramana B V, Sarma P V G K and 2 more
Genomic diversity and functional insights of carbapenem-resistant Klebsiella pneumoniae revealed by centroid coding sequences analysis.
Microbial genomics | 2025-07-01 | PMID 40711476
Cao Jianghong, Xue Dongdong, Gao Dan and 4 more
Digital phenotyping for migraine: A game-changer for research and management.
Cephalalgia : an international journal of headache | 2025-07-01 | PMID 40734464
Petrušić Igor
Hypokalaemia and bradycardia unmask the loss-of-function phenotype of a Brugada Syndrome SCN5A mutation.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology | 2026-02-03 | PMID 40743271
Frosio Anthony, Marchese Procolo, Bertoli Giorgia and 18 more
Genes: SCN5A
Effects of DNA methylation and polygenic scores on self-reported suicidal ideation in psychoses: no evidence of epigenetic basis of polygenic risk.
Psychiatric genetics | 2025-10-01 | PMID 40762416
Nader George, Ducharme Matisse, Gerretsen Philip and 3 more
The Caenorhabditis elegans spe-21 gene that encodes a palmitoyltransferase is necessary for spermiogenesis.
Developmental biology | 2025-11-01 | PMID 40784522
Suryanarayanan Saai, Chen Dawn S, Zuo Yamei and 5 more
Unravelling the genetic landscape of Channa argus in Shandong Province: Insights into population differentiation, adaptation and conservation from whole-genome resequencing.
Journal of fish biology | 2025-11-01 | PMID 40798995
An Li, Meng Qinglei, Dong Xuesa and 7 more
SLC6A3 gene methylation may be associated with alcohol use disorder, but personality and life stress may not influence methylation.
CNS spectrums | 2025-08-15 | PMID 40814263
Chyou Te-En, Kuo Shin-Chang, Yeh Yi-Wei and 5 more
Genes: SLC6A3
Investigation of delamanid, bedaquiline, and linezolid resistance rates and related gene mutations in multidrug-resistant Mycobacterium tuberculosis in regional tuberculosis reference laboratories of Iran.
BMC microbiology | 2025-08-15 | PMID 40817101
Ahmad Khosravi Nazanin, Khosravi Azar Dokht, Hashemzadeh Mohammad and 2 more
Quantitative genotoxicity assessment of N-nitrosodimethylamine in mice by error-corrected next-generation sequencing and DNA methylation quantification for toxicity threshold determination.
Archives of toxicology | 2025-11-01 | PMID 40849524
You Xinyue, Sun Chen, Cao Yiyi and 5 more
[Parkinson's Disease Associated with Mutations in the LRRK2 Gene: Approaches to Therapy].
Molekuliarnaia biologiia | 2025-01-01 | PMID 40864855
Usenko T S, Pchelina S N
Phenotype Analysis in Two Families With Otopalatodigital Syndrome Spectrum Disorder Based on FLNA Gene Variants.
Clinical genetics | 2026-03-01 | PMID 40884164
Schwarz Martin, Fišer Miroslav, Šodková Lenka and 8 more
Genes: FLNA
Trio exome sequencing of an optic nerve hypoplasia cohort reveals evidence for polygenic architecture.
Ophthalmic genetics | 2025-12-01 | PMID 40887606
Aparicio Jennifer G, Stachelek Kevin, Garcia-Filion Pamela and 6 more
Cytoplasmic inter-subunit interface modulates TRPC5 activity: Molecular mechanism behind intellectual disability-related R175C mutation.
Neurobiology of disease | 2025-10-15 | PMID 40907672
Mitro Michal, Ptáková Alexandra, Vlachová Viktorie and 1 more
Genes: TRPC5
Investigating the Relationship Between Mutations in gyrA and parC Genes and Resistance to Fluoroquinolones in Uropathogenic Escherichia coli Isolates.
Microbial drug resistance (Larchmont, N.Y.) | 2025-10-01 | PMID 40930569
Ghaffari Lashkenari Erfan, Mir Maryam Sadat, Mohammadi Mohsen and 2 more
Pathological Endotypic Traits of Paediatric Obstructive Sleep Apnea: Age and Sex Differences.
Respirology (Carlton, Vic.) | 2026-01-01 | PMID 40937486
Lin Chien-Heng, Hang Liang-Wen, Finnsson Eysteinn and 3 more
Gene body methylation regulates gene expression and mediates phenotypic diversity in natural Arabidopsis populations.
Nature plants | 2025-10-01 | PMID 40940427
Shahzad Zaigham, Hollwey Elizabeth, Moore Jonathan D and 5 more
Bi-allelic INTU variants define a ciliopathy disorder characterized by orofacial, digital, and cardiac anomalies.
HGG advances | 2026-01-15 | PMID 40968537
Rushforth Rebekah, Reynolds Kurt, Estes Steven I and 5 more
Genes: INTU
Genetic and Clinical Investigations of C12orf65 Gene Mutations in Three Chinese Pedigrees.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society | 2026-06-01 | PMID 40993840
Jia Yiran, Huang Zhiqin, Chen Chunli and 2 more
Genes: OPA1
Dissecting the genetic architecture of circadian rhythms in human tissues using a quantitative circadian deviation score.
Genome biology | 2025-09-25 | PMID 40999520
Li Zheyu, Chen Liang
Real-world treatment adherence and persistence of FLT3 inhibitors as post-alloHCT maintenance therapy in patients with AML in the United States: a cohort study using administrative claims data.
Leukemia & lymphoma | 2025-12-01 | PMID 41041900
Kennedy Vanessa E, Touya Maelys, Spalding James and 5 more
Genes: FLT3, PDC
Novel Loss-of-Function Variant, Cys1384Phe, in SCN5A Is Associated With an Overlapping Phenotype of Brugada Syndrome, Sick Sinus Syndrome, and Dilated Cardiomyopathy.
Circulation journal : official journal of the Japanese Circulation Society | 2025-12-25 | PMID 41047353
Yamauchi Kohei, Kato Koichi, Ohno Seiko and 8 more
Genes: SCN5A
Association between single-nucleotide polymorphism rs868875 of CLEC4M gene and clinical severity of COVID-19 in a Brazilian population.
Immunogenetics | 2025-10-09 | PMID 41062837
Galisa Steffany Larissa Galdino, de Oliveira Sá Marcus Villander Barros, Tavares Natália Machado and 8 more
Genes: CLEC4M
Impact of IL-17A rs2275913 allelic variation on periodontitis susceptibility: evidence from a meta-analysis.
Odontology | 2026-07-01 | PMID 41071529
Zhang Jiawei, Xu Shulan
PCR-CRISPR/Cas12a-based fluorescence and lateral flow dipstick platforms for efficient screening of CD71 biallelic mutants.
Analytica chimica acta | 2025-11-22 | PMID 41073016
Nie Yuxin, Wang Wanjie, Wang Nan and 6 more
Correlation of QRDR mutations and MIC levels in fluoroquinolone-resistant Staphylococcus aureus clinical isolates.
Microbiology spectrum | 2025-11-04 | PMID 41081515
Kim Sohyeong, Xuan Xianglan, Jung Minju and 8 more
From genotype to phenotype with 1,086 near telomere-to-telomere yeast genomes.
Nature | 2025-12-01 | PMID 41094142
Loegler Victor, Thiele Pia, Teyssonnière Elie and 9 more
Functional dissection of H3K4 methyltransferases reveals distinct catalytic and non-catalytic roles in C. elegans development.
Development (Cambridge, England) | 2025-11-01 | PMID 41122790
Attianese Benedetta, Wang Hua, Madsen Katrine and 4 more
Genes: SET
Association between MASP2 gene polymorphisms and susceptibility to Covid-19 in Iranian patients: a case-control study.
BMC infectious diseases | 2025-10-24 | PMID 41136953
Jabbari Maryam, Ghaffari Hadi, Ghaffari Kazem and 4 more
Genes: MASP2
Association of IFNL4 and IFITM3 Genetic Variants with Susceptibility to HCV-Related Liver Cirrhosis and Hepatocellular Carcinoma.
Asian Pacific journal of cancer prevention : APJCP | 2025-10-01 | PMID 41148623
Osman Enas Ahmed, Mohamed Marwa Ahmed, Abbas Rania M and 4 more
Genes: IFITM3