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Academic Journal

Association of TIMP2 418 G/C and MMP Gene Polymorphism with Risk of Urinary Cancers: Systematic Review and Meta-analysis.

  • Authors : Gowtham P; Medical Bionanotechnology, Faculty of Allied Health Sciences, Chettinad Hospital and Research Institute (CHRI), Chettinad Academy of Research and Education (CARE), Chennai, India.; Girigoswami K

Subjects: Polymorphism, Single Nucleotide*/Polymorphism, Single Nucleotide*/Polymorphism, Single Nucleotide*/genetics ; Tissue Inhibitor of Metalloproteinase-2*/Tissue Inhibitor of Metalloproteinase-2*/Tissue Inhibitor of Metalloproteinase-2*/genetics ; Urologic Neoplasms*/Urologic Neoplasms*/Urologic Neoplasms*/genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2024 Mar; Vol. 28 (3), pp. 83-90. Date of Electronic Publication: 2024 Mar 13.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Prediction of MicroRNA-Disease Potential Association Based on Sparse Learning and Multilayer Random Walks.

  • Authors : Yao HB; Computer Science and Artificial Intelligence and Aliyun School of Big Data, Changzhou University, Changzhou, China.; Hou ZJ

Subjects: MicroRNAs*/MicroRNAs*/MicroRNAs*/genetics; Humans ; Algorithms

  • Source: Journal of computational biology : a journal of computational molecular cell biology [J Comput Biol] 2024 Mar; Vol. 31 (3), pp. 241-256. Date of Electronic Publication: 2024 Feb Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 9433358 Publication Model: Print-Electronic

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Academic Journal

Vitamin D Receptor Polymorphisms in a Spanish Cohort of Parkinson's Disease Patients.

  • Authors : Canales-Cortés S; Departamento de Bioquímica y Biología Molecular y Genética, Facultad de Enfermería y Terapia Ocupacional, Universidad de Extremadura, Cáceres, Spain.; Instituto Universitario de Investigación Biosanitaria de Extremadura (INUBE), Cáceres, Spain.

Subjects: Imidoesters* ; Parkinson Disease*/Parkinson Disease*/Parkinson Disease*/genetics ; Receptors, Calcitriol*/Receptors, Calcitriol*/Receptors, Calcitriol*/genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2024 Feb; Vol. 28 (2), pp. 59-64.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Association of Interleukin-17A and Interleukin-17F Gene Polymorphisms with Atopic Dermatitis in Chinese Children.

  • Authors : Shen C; Information Center, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.; Sino-Finland Joint AI Laboratory for Child Health of Zhejiang Province, Hangzhou, China.

Subjects: Dermatitis, Atopic*/Dermatitis, Atopic*/Dermatitis, Atopic*/genetics ; Interleukin-17*/Interleukin-17*/Interleukin-17*/genetics; Child

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2024 Feb; Vol. 28 (2), pp. 43-49.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Genetic Variants of Steroidogenesis and Gonadotropin Pathways and Polycystic Ovary Syndrome Susceptibility: A Systematic Review and Meta-analysis.

  • Authors : Sharma P; Laboratory for Reproductive and Developmental Disorders, Department of Human Genetics and Molecular Medicine, School of Health Sciences, Central University of Punjab, Bathinda, India.; Kumar Singh A

Subjects: Polycystic Ovary Syndrome*/Polycystic Ovary Syndrome*/Polycystic Ovary Syndrome*/genetics; Female ; Humans

  • Source: Metabolic syndrome and related disorders [Metab Syndr Relat Disord] 2024 Feb; Vol. 22 (1), pp. 15-26. Date of Electronic Publication: 2023 Oct 25.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101150318 Publication Model: Print-Electronic

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Academic Journal

Interaction Between Genetic Susceptibility and COVID-19 Pathogenesis in Pediatric Multisystem Inflammatory Disorders: The Role of Immune Responses.

  • Authors : Chen LN; Department of Pediatric, Affiliated Hospital of Shaoxing University, Shaoxing, China.; Shou ZX

Subjects: COVID-19*/COVID-19*/COVID-19*/*complications; COVID-19*/COVID-19*/COVID-19*/genetics ; COVID-19*/COVID-19*/COVID-19*/epidemiology pediatric multisystem inflammatory disease, COVID-19 related

  • Source: Viral immunology [Viral Immunol] 2024 Jan-Feb; Vol. 37 (1), pp. 1-11. Date of Electronic Publication: 2024 Jan 25.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 8801552 Publication Model: Print-Electronic

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Editorial & Opinion

A Novel Genetic Candidate for Primary Lymphedema.

  • Authors : Rockson SG; Stanford University School of Medicine, Stanford, California, USA.

Subjects: Genetic Predisposition to Disease* ; Lymphedema*/Lymphedema*/Lymphedema*/diagnosis ; Lymphedema*/Lymphedema*/Lymphedema*/genetics

  • Source: Lymphatic research and biology [Lymphat Res Biol] 2022 Oct; Vol. 20 (5), pp. 467.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101163587 Publication Model: Print Cited

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Academic Journal

The Association Between the PTPN22 C1858T Variant and Vasculitis: A Meta-analysis Update with Trial Sequential Analysis.

  • Authors : Lee YH; Division of Rheumatology, Korea University Anam Hospital, Seoul, Korea.; Song GG

Subjects: Genetic Predisposition to Disease*/Genetic Predisposition to Disease*/Genetic Predisposition to Disease*/genetics ; Vasculitis*/Vasculitis*/Vasculitis*/genetics; Humans

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2022 Oct; Vol. 26 (10), pp. 492-500.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Investigating the Association of MTHFR C677T Gene Polymorphism with Recurrent Spontaneous Abortion Among Azerbaijani Women from Northwest Iran.

  • Authors : Moqadami A; Department of Animal Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran.; Rezaei A

Subjects: Polymorphism, Genetic*/Polymorphism, Genetic*/Polymorphism, Genetic*/genetics ; Abortion, Habitual*/Abortion, Habitual*/Abortion, Habitual*/genetics; Pregnancy

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2023 Oct; Vol. 27 (10), pp. 339-344. Date of Electronic Publication: 2023 Oct Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Altered Vitamin D Receptor Expression in Apa-I (rs7975232) Allelic Variants-A Probable Risk Factor for Susceptibility to Hepatitis B Virus Infection and Disease Progression.

  • Authors : Kalita MJ; Laboratory of Molecular Virology and Oncology (LMVO), Department of Bioengineering and Technology, Gauhati University, Guwahati, Assam, India.; Kalita S

Subjects: Hepatitis B*/Hepatitis B*/Hepatitis B*/genetics ; Hepatitis B virus* ; Receptors, Calcitriol*/Receptors, Calcitriol*/Receptors, Calcitriol*/genetics

  • Source: Viral immunology [Viral Immunol] 2023 Oct; Vol. 36 (8), pp. 534-543. Date of Electronic Publication: 2023 Sep 05.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 8801552 Publication Model: Print-Electronic

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Academic Journal

Association of Apolipoprotein A5 Gene Variants with Hyperlipidemic Acute Pancreatitis in Southeastern China.

  • Authors : Li Y; Department of Gastroenterology, The First Hospital of Quanzhou Affiliated to Fujian Medical University, Quanzhou, China.; Cai H

Subjects: Apolipoproteins A*/Apolipoproteins A*/Apolipoproteins A*/genetics ; Pancreatitis*/Pancreatitis*/Pancreatitis*/genetics; Humans

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2023 Sep; Vol. 27 (9), pp. 284-289.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

A Splicing Transcriptome-Wide Association Study Identifies Candidate Altered Splicing for Prostate Cancer Risk.

  • Authors : Sun Y; College of Life Science, Longyan University, Longyan, P.R. China.; Cancer Epidemiology Division, Population Sciences in the Pacific Program, University of Hawaii Cancer Center, University of Hawaii at Manoa, Honolulu, Hawaii, USA.

Subjects: Transcriptome*/Transcriptome*/Transcriptome*/genetics ; Prostatic Neoplasms*/Prostatic Neoplasms*/Prostatic Neoplasms*/genetics; Male

  • Source: Omics : a journal of integrative biology [OMICS] 2023 Aug; Vol. 27 (8), pp. 372-380. Date of Electronic Publication: 2023 Jul 25.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101131135 Publication Model: Print-Electronic

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Academic Journal

Association Between X-Ray Repair Cross-Complementing Group 1 Arg399Gln Polymorphism and Risk of Oral Leukoplakia: A Meta-analysis.

  • Authors : Wang J; Department of Pharmacy, Peking University First Hospital, Xicheng District, Beijing, China.; Zhu C

Subjects: Genetic Predisposition to Disease*/Genetic Predisposition to Disease*/Genetic Predisposition to Disease*/genetics ; Polymorphism, Single Nucleotide*/Polymorphism, Single Nucleotide*/Polymorphism, Single Nucleotide*/genetics; Asian People/Asian People/Asian People/genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Dec; Vol. 25 (12), pp. 781-787. Date of Electronic Publication: 2021 Dec Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

C Deletion at the re74650330 Locus of the SLC39A8 Gene (rs74650330) Increases the Risk of Coronary Artery Disease in Individuals with Low-Density Lipoprotein Cholesterol Levels.

  • Authors : Zhang J; Clinical Medical Research Center, Changzhou Key Laboratory of Individualized Diagnosis and Treatment Associated with High Technology Research, The Third Affiliated Hospital of Soochow University, Changzhou, China.; Yu Y

Subjects: Genetic Predisposition to Disease*; Cation Transport Proteins/Cation Transport Proteins/Cation Transport Proteins/*genetics ; Cholesterol, LDL/Cholesterol, LDL/Cholesterol, LDL/*blood

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Oct; Vol. 25 (10), pp. 660-667.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

A Common Variant at 11q23.3 Is Associated with Susceptibility to Atopic Dermatitis in the Han Chinese Population.

  • Authors : Li Y; Department of Dermatology, First Affiliated Hospital, Anhui Medical University, Hefei, China.; Key Laboratory of Dermatology (Anhui Medical University), Ministry of Education, Hefei, China.

Subjects: Genetic Loci* ; Genetic Predisposition to Disease*; Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Oct; Vol. 25 (10), pp. 638-645. Date of Electronic Publication: 2021 Oct Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

PCSK9 E670G (rs505151) Variant and Coronary Artery Disease Risk Among Diabetics.

  • Authors : Mohamed SH; Medical Biochemistry Department, and Faculty of Medicine, University of Zagazig, Zagazig, Egypt.; Hassaan MMM

Subjects: Genetic Predisposition to Disease*; Coronary Artery Disease/Coronary Artery Disease/Coronary Artery Disease/*genetics ; Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/*complications

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Sep; Vol. 25 (9), pp. 615-623.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Common Variants of the OPG gene Are Associated with Osteoporosis Risk: A Meta-Analysis.

  • Authors : Li X; Department of Orthopedic Trauma, Yuncheng Central Hospital, Shanxi Medical University, Yuncheng, China.; Cheng J

Subjects: Genetic Predisposition to Disease*; Osteoporosis/Osteoporosis/Osteoporosis/*genetics ; Osteoprotegerin/Osteoprotegerin/Osteoprotegerin/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Sep; Vol. 25 (9), pp. 600-610. Date of Electronic Publication: 2021 Sep 09.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Association of the MYH6 Gene Polymorphism with the Risk of Atrial Fibrillation and Warfarin Anticoagulation Therapy.

  • Authors : Fu T; Department of Cardiology, Yiwu Central Hospital, Yiwu, China.; Chen M

Subjects: Genetic Predisposition to Disease*; Anticoagulants/Anticoagulants/Anticoagulants/*therapeutic use ; Atrial Fibrillation/Atrial Fibrillation/Atrial Fibrillation/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Sep; Vol. 25 (9), pp. 590-599. Date of Electronic Publication: 2021 Sep 09.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Association Between the SLC2A2 Gene rs1499821 Polymorphism and Caries Susceptibility.

  • Authors : Liu L; Guangxi Medical University College of Stomatology, Nanning, China.; Ma F

Subjects: Dental Caries*/Dental Caries*/Dental Caries*/genetics ; Glucose Transporter Type 2*/Glucose Transporter Type 2*/Glucose Transporter Type 2*/genetics; Child

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2023 May; Vol. 27 (5), pp. 149-156.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Editorial & Opinion

Re: "Association of the Interleukin 1B-31*C Proinflammatory Allele with the Severity of COVID-19 Patients: A Preliminary Report" by Galán-Huerta et al.

Subjects: COVID-19*; Humans ; Alleles

  • Source: Viral immunology [Viral Immunol] 2023 May; Vol. 36 (4), pp. 298. Date of Electronic Publication: 2023 Mar 31.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 8801552 Publication Model: Print-Electronic

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Academic Journal

Association of BRCA2 Gene Functional Polymorphisms with Nonsyndromic Cleft Lip With or Without Cleft Palate in a Chinese Population.

  • Authors : Guo S; Department of Oral and Maxillofacial Plastic and Traumatic Surgery, Beijing Stomatological Hospital, Capital Medical University, Beijing, China.; Zhou Z

Subjects: Cleft Palate*/Cleft Palate*/Cleft Palate*/genetics ; Cleft Lip*/Cleft Lip*/Cleft Lip*/genetics ; MicroRNAs*/MicroRNAs*/MicroRNAs*/genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2023 May; Vol. 27 (5), pp. 157-164. Date of Electronic Publication: 2023 May 18.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Correlation Between Polymorphisms of the SIRT1 Gene microRNA Target Sites and Diabetic Nephropathy.

  • Authors : Sun Y; Department of Endocrinology and Metabolism, Zhuji People's Hospital of Zhejiang Province, Zhuji, China.; Wang J

Subjects: Genetic Predisposition to Disease*; Diabetic Nephropathies/Diabetic Nephropathies/Diabetic Nephropathies/*genetics ; Sirtuin 1/Sirtuin 1/Sirtuin 1/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Jun; Vol. 25 (6), pp. 387-398.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Influence of Lysyl oxidase Polymorphisms in Cancer Risk: An Updated Meta-analysis.

Subjects: Genetic Predisposition to Disease*; Biomarkers, Tumor/Biomarkers, Tumor/Biomarkers, Tumor/*genetics ; Carcinogenesis/Carcinogenesis/Carcinogenesis/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Jun; Vol. 25 (6), pp. 411-418. Date of Electronic Publication: 2021 May 27.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Association of SNPs in Lipid Metabolism Gene Single Nucleotide Polymorphism with the Risk of Obesity in Children.

  • Authors : Kulaeva ED; Biology of Development and Genome Organization Laboratory, Department of Genetics, Southern Federal University Rostov-on-Don, Russia.; Volchik VV

Subjects: Genetic Predisposition to Disease*; Lipid Metabolism/Lipid Metabolism/Lipid Metabolism/*genetics ; Pediatric Obesity/Pediatric Obesity/Pediatric Obesity/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Jun; Vol. 25 (6), pp. 419-425.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Lipoprotein Lipase Gene Polymorphisms Are Associated with Myocardial Infarction Risk: A Meta-Analysis.

  • Authors : He K; Department of Cardiology, The First Affiliated Hospital, Changsha Medical University, Changsha, People's Republic of China.; School of Clinic Medical Science, Changsha Medical University, Changsha, People's Republic of China.

Subjects: Genetic Predisposition to Disease*; Lipoprotein Lipase/Lipoprotein Lipase/Lipoprotein Lipase/*genetics ; Myocardial Infarction/Myocardial Infarction/Myocardial Infarction/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Jun; Vol. 25 (6), pp. 434-444.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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