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Succinic semialdehyde dehydrogenase deficiency: a metabolic and genomic approach to diagnosis.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1405468
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Causal association between phenylalanine and Parkinson's disease: a two-sample bidirectional mendelian randomization study.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1322551
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Causality of genetically determined metabolites on susceptibility to prevalent urological cancers: a two-sample Mendelian randomization study and meta-analysis.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1398165
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Bioinformatics analysis of the association between obesity and gastric cancer.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1385559
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Causal relationships between lung cancer and sepsis: a genetic correlation and multivariate mendelian randomization analysis.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1381303
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Mendelian randomization and Bayesian model averaging of autoimmune diseases and Long COVID.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1383162
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Identification of an immune-related gene prognostic index for predicting survival and immunotherapy efficacy in papillary renal cell carcinoma.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2022.970900
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Corrigendum: Identification of an immune-related gene prognostic index for predicting survival and immunotherapy efficacy in papillary renal cell carcinoma.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1440802
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Development and evaluation of a chronic kidney disease risk prediction model using random forest.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1409755
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Association between genetically proxied glucosamine and risk of cancer and non-neoplastic disease: A Mendelian randomization study.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1293668
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Lactylation: The emerging frontier in post-translational modification.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1423213
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Identification of differentially expressed genes of blood leukocytes for Schizophrenia.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1398240
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Editorial: Searching for causes of infertility: from pathophysiologic mechanisms to therapeutic strategies.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1432026
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Effects of ankylosing spondylitis on cardiovascular disease: aMendelian randomization study.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1359829
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Editorial: Neuronal ceroid lipofuscinosis: molecular genetics and epigenetics.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1430703
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Association of ankylosing spondylitis with cardiovascular disease: a bidirectional two-sample mendelian randomization study.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1260247
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DeepSplice: a deep learning approach for accurate prediction of alternative splicing events in the human genome.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1349546
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Causal association between major depressive disorder and venous thromboembolism: a bidirectional mendelian randomization study.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1383333
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Inside the genome: understanding genetic influences on oxidative stress.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1397352
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The genomic landscape of the immune system in lung cancer: present insights and continuing investigations.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1414487
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Tuning tRNAs for improved translation.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1436860
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Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1437233
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- Article
How does the age of control individuals hinder the identification of target genes for Huntington's disease?
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1377237
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Case report: A case of Rabson-Mendenhall syndrome: long-term follow-up and therapeutic management with empagliflozin.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1414451
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N6-methyladenosine methylation analysis of circRNAs in acquired middle ear cholesteatoma.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1396720
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A rare missense p.C125Y mutation in the TNFRSF1A gene identified in a Chinese family with tumor necrosis factor receptor-associated periodic fever syndrome.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1413641
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Application of whole exome sequencing in carrier screening for high-risk families without probands.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1415811
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Leveraging genetics to investigate causal effects of immune cell phenotypes in periodontitis: a mendelian randomization study.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1382270
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Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1384094
- Publication type:
- Article
Endometriosis is a disease of immune dysfunction, which could be linked to microbiota.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1386411
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Phylogenomic analysis and molecular identification of true fruit flies.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1414074
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A novel variation in DEPDC5 causing familial focal epilepsy with variable foci.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1414259
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Integrative analysis of cancer multimodality data identifying COPS5 as a novel biomarker of diffuse large B-cell lymphoma.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1407765
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Robust evidence supports a causal link between higher birthweight and longer telomere length: a mendelian randomization study.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1264028
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ZP1-Y262C mutation causes abnormal zona pellucida formation and female infertility in humans.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1407202
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Editorial: Inborn errors of carbohydrate metabolism.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1430414
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Assessing causality between obstructive sleep apnea with the dyslipidemia and osteoporosis: a Mendelian randomization study.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1359108
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Emotional dispositions and intracerebral hemorrhage: a Mendelian Randomization insight.
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- Frontiers in Genetics, 2024, p. 1
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A causal link between circulating leukocytes and three major urologic cancers: a mendelian randomization investigation.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1424119
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Bridging the gap: exploring the causal relationship between metformin and tumors.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1397390
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Neutrophil in the suppressed immune microenvironment: Critical prognostic factor for lung adenocarcinoma patients with KEAP1 mutation.
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- Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1382421
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Prenatal diagnosis and family analysis of 17q12 microdeletion syndrome with fetal renal abnormalities.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1401315
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The causal relationship between smoking, alcohol consumption, and renal clear cell carcinoma: a Mendelian randomization study.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1391542
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Identification of DNA motif pairs on paired sequences based on composite heterogeneous graph.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1424085
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A novel insertional allele of the CG18135 gene is associated with severe mutant phenotypes in Drosophila melanogaster.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1355368
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A comparative analysis of RNA-Seq and NanoString technologies in deciphering viral infection response in upper airway lung organoids.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1327984
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Bipartite networks represent causality better than simple networks: evidence, algorithms, and applications.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1371607
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Identifying genomic variant associated with long QT syndrome type 2 in an ecuadorian mestizo individual: a case report.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1395012
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Quantifying spatial CXCL9 distribution with image analysis predicts improved prognosis of triple-negative breast cancer.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1421573
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Comprehensive transcriptomic analysis identifies SLC25A4 as a key predictor of prognosis in osteosarcoma.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1410145
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