المؤلفون: Sierra-Díaz DC; School of Medicine and Health Sciences, Center for Research in Genetics and Genomics (CIGGUR), Institute of Translational Medicine (IMT), Universidad Del Rosario, Bogotá, Colombia., Morel A; School of Medicine and Health Sciences, Center for Research in Genetics and Genomics (CIGGUR), Institute of Translational Medicine (IMT), Universidad Del Rosario, Bogotá, Colombia., Fonseca-Mendoza DJ; School of Medicine and Health Sciences, Center for Research in Genetics and Genomics (CIGGUR), Institute of Translational Medicine (IMT), Universidad Del Rosario, Bogotá, Colombia., Bravo NC; School of Medicine and Health Sciences, Center for Research in Genetics and Genomics (CIGGUR), Institute of Translational Medicine (IMT), Universidad Del Rosario, Bogotá, Colombia., Molano-Gonzalez N; Clinical Research Group, School of Medicine and Health Science, Universidad del Rosario, Bogotá, Colombia., Borras M; Fundación Cardioinfantil, Instituto de Cardiología, Bogotá, Colombia., Munevar I; Fundación Cardioinfantil, Instituto de Cardiología, Bogotá, Colombia., Lema M; Clínica de Oncología Astorga, Medellín, Colombia., Idrobo H; Centro Médico Julián Coronel, Cali, Colombia., Trujillo D; Centro Médico Julián Coronel, Cali, Colombia., Serrano N; Hospital Internacional de Colombia HIC, Piedecuesta, Colombia., Orduz AI; Hospital Internacional de Colombia HIC, Piedecuesta, Colombia., Lopera D; Oncólogos del Occidente S.A.S, Manizales, Colombia., González J; Oncólogos del Occidente S.A.S, Manizales, Colombia., Rojas G; Oncólogos del Occidente S.A.S, Manizales, Colombia.; Oncologos del Occidente SAS, Pereira, Colombia., Londono-De Los Ríos P; Oncólogos del Occidente S.A.S, Manizales, Colombia.; Oncologos del Occidente SAS, Pereira, Colombia., Manneh R; SOHEC, Sociedad de Oncología y Hematología del Cesar, Valledupar, Colombia., Cabrera R; School of Medicine and Health Sciences, Center for Research in Genetics and Genomics (CIGGUR), Institute of Translational Medicine (IMT), Universidad Del Rosario, Bogotá, Colombia.; Laboratorio de Biología Molecular y Pruebas Diagnósticas de Alta Complejidad, Fundación Cardioinfantil-Instituto de Cardiología, Bogotá, Colombia., Rubiano W; Hospital Universitario Mayor Méderi, Bogotá, Colombia., de la Peña J; Hospital Universitario Mayor Méderi, Bogotá, Colombia., Quintero MC; Integrative IPS, Bogotá, Colombia., Mantilla W; Fundación Cardioinfantil, Instituto de Cardiología, Bogotá, Colombia.; Fundación CTIC-Fundación Cardioinfantil, Instituto de Cardiología, Bogotá, Colombia., Restrepo CM; School of Medicine and Health Sciences, Center for Research in Genetics and Genomics (CIGGUR), Institute of Translational Medicine (IMT), Universidad Del Rosario, Bogotá, Colombia. carlos.restrepo@urosario.edu.co.

المصدر: Human genomics [Hum Genomics] 2024 Jun 18; Vol. 18 (1), pp. 68. Date of Electronic Publication: 2024 Jun 18.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101202210 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-7364 (Electronic) Linking ISSN: 14739542 NLM ISO Abbreviation: Hum Genomics Subsets: MEDLINE

مواضيع طبية MeSH: Germ-Line Mutation*/genetics , Breast Neoplasms*/genetics , Breast Neoplasms*/pathology , Breast Neoplasms*/epidemiology , Genetic Predisposition to Disease* , BRCA2 Protein*/genetics, Humans ; Female ; Colombia/epidemiology ; Middle Aged ; Adult ; BRCA1 Protein/genetics ; Exome Sequencing ; Aged ; Genetic Testing/methods ; Ataxia Telangiectasia Mutated Proteins/genetics

المؤلفون: Armstrong ND; Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA. nmda@uab.edu., Patki A; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA., Srinivasasainagendra V; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA., Ge T; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA., Lange LA; Division of Biomedical Informatics and Personalized Medicine, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA., Kottyan L; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA., Namjou B; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA., Shah AS; Department of Pediatrics, Cincinnati Children's Hospital Medical Center &, The University of Cincinnati, Cincinnati, OH, USA., Rasmussen-Torvik LJ; Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA., Jarvik GP; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA., Meigs JB; Division of General Internal Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.; Department of Medicine, Harvard Medical School, Boston, MA, USA.; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA, USA., Karlson EW; Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.; Mass General Brigham Personalized Medicine, Boston, MA, USA., Limdi NA; Department of Neurology, University of Alabama at Birmingham, Birmingham, AL, USA., Irvin MR; Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA., Tiwari HK; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA.

المصدر: Scientific reports [Sci Rep] 2024 Jun 18; Vol. 14 (1), pp. 14009. Date of Electronic Publication: 2024 Jun 18.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE

مواضيع طبية MeSH: Diabetes Mellitus, Type 2*/genetics , Black or African American*/genetics , Genome-Wide Association Study* , Genetic Predisposition to Disease*, Humans ; Male ; Female ; Middle Aged ; Aged ; Polymorphism, Single Nucleotide ; Linkage Disequilibrium ; Phenotype ; Multifactorial Inheritance/genetics

المؤلفون: Ciocarlie T; Department VII Internal Medicine II, Discipline of Cardiology, University of Medicine and Pharmacy 'Victor Babes', 300041 Timisoara, Romania., Motofelea AC; Department of Internal Medicine, University of Medicine and Pharmacy 'Victor Babes', 300041 Timisoara, Romania., Motofelea N; Department of Obstetrics and Gynecology, University of Medicine and Pharmacy 'Victor Babes', Eftimie Murgu Sq. No. 2, 300041 Timisoara, Romania., Dutu AG; Department of Molecular Sciences, Iuliu Hațieganu University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania., Crăciun A; Department of Molecular Sciences, Iuliu Hațieganu University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania., Costachescu D; Radiology Department, University of Medicine and Pharmacy 'Victor Babes', 300041 Timisoara, Romania., Roi CI; Multidisciplinary Center for Research, Evaluation, Diagnosis and Therapies in Oral Medicine, University of Medicine and Pharmacy 'Victor Babes', Eftimie Murgu Sq. No. 2, 300041 Timisoara, Romania., Silaghi CN; Department of Molecular Sciences, Iuliu Hațieganu University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania., Crintea A; Department of Molecular Sciences, Iuliu Hațieganu University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.

المصدر: International journal of molecular sciences [Int J Mol Sci] 2024 Jun 17; Vol. 25 (12). Date of Electronic Publication: 2024 Jun 17.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE

مواضيع طبية MeSH: Receptors, Calcitriol*/genetics , Lung Neoplasms*/genetics , Vitamin D*/metabolism , Polymorphism, Single Nucleotide* , Genetic Predisposition to Disease*, Humans ; Risk Factors

المؤلفون: Lin WD; Department of Medical Research, China Medical University Hospital, Taichung, 404327, Taiwan.; School of Post Baccalaureate Chinese Medicine, China Medical University, Taichung, 404333, Taiwan., Liao WL; Graduate Institute of Integrated Medicine, College of Chinese Medicine, China Medical University, Taichung, 404333, Taiwan.; Center for Personalized Medicine, China Medical University Hospital, Taichung, 404327, Taiwan., Chen WC; Department of Internal Medicine, Pulmonary and Critical Care Medicine, China Medical University Hospital, Taichung, 404333, Taiwan.; Graduate Institute of Biomedical Sciences, China Medical University, Taichung, 404327, Taiwan., Liu TY; Department of Medical Research, Million-Person Precision Medicine Initiative, China Medical University Hospital, Taichung, 404327, Taiwan., Chen YC; Department of Medical Research, Million-Person Precision Medicine Initiative, China Medical University Hospital, Taichung, 404327, Taiwan., Tsai FJ; Department of Medical Research, China Medical University Hospital, Taichung, 404327, Taiwan. 000704@tool.caaumed.org.tw.; School of Chinese Medicine, China Medical University, Taichung, 404333, Taiwan. 000704@tool.caaumed.org.tw.; Division of Genetics and Metabolism, China Medical University Children's Hospital, Taichung, 404327, Taiwan. 000704@tool.caaumed.org.tw.; Department of Medical Genetics, China Medical University Hospital, Taichung, 404327, Taiwan. 000704@tool.caaumed.org.tw.; Department of Medical Laboratory Science and Biotechnology, Asia University, Taichung, 413305, Taiwan. 000704@tool.caaumed.org.tw.; Department of Medical Research, China Medical University Hospital, No. 2, Yude Road, North District, Taichung, 404327, Taiwan. 000704@tool.caaumed.org.tw.

المصدر: BMC genomics [BMC Genomics] 2024 Jun 17; Vol. 25 (1), pp. 607. Date of Electronic Publication: 2024 Jun 17.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 100965258 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2164 (Electronic) Linking ISSN: 14712164 NLM ISO Abbreviation: BMC Genomics Subsets: MEDLINE

مواضيع طبية MeSH: Pulmonary Disease, Chronic Obstructive*/genetics , Genome-Wide Association Study* , Genetic Predisposition to Disease* , Polymorphism, Single Nucleotide*, Humans ; Taiwan ; Male ; Female ; Aged ; Multifactorial Inheritance ; Case-Control Studies ; Middle Aged ; Risk Factors ; Genetic Loci ; Asian People/genetics ; Genetic Risk Score

المؤلفون: Wang Q; Department of Urology, Jianhu Clinical Medical College of Yangzhou University, No. 666 South Ring Road, Yancheng, Jiangsu Province, 224700, China., Chen S; Department of Urology, Jianhu Clinical Medical College of Yangzhou University, No. 666 South Ring Road, Yancheng, Jiangsu Province, 224700, China., Wang G; Department of Urology, Jianhu Clinical Medical College of Yangzhou University, No. 666 South Ring Road, Yancheng, Jiangsu Province, 224700, China., Zhang T; Department of Urology, Jianhu Clinical Medical College of Yangzhou University, No. 666 South Ring Road, Yancheng, Jiangsu Province, 224700, China., Gao Y; Department of Urology, Jianhu Clinical Medical College of Yangzhou University, No. 666 South Ring Road, Yancheng, Jiangsu Province, 224700, China. gaoyulong202204@163.com.

المصدر: BMC cancer [BMC Cancer] 2024 Jun 17; Vol. 24 (1), pp. 739. Date of Electronic Publication: 2024 Jun 17.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 100967800 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2407 (Electronic) Linking ISSN: 14712407 NLM ISO Abbreviation: BMC Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Quantitative Trait Loci* , Mendelian Randomization Analysis* , Kidney Neoplasms*/genetics , Genetic Predisposition to Disease*, Humans ; Polymorphism, Single Nucleotide ; Genome-Wide Association Study

المؤلفون: Boutros A; Skin Cancer Unit, Medical Oncology 2, IRCCS Ospedale Policlinico San Martino, Genova, Italy. boutros.andrea@gmail.com.; Department of Internal Medicine and Medical Specialties (DIMI), School of Medicine, University of Genoa, Genova, Italy. boutros.andrea@gmail.com., Carosio R; Tumor Epigenetics Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy., Campanella D; Clinical Epidemiology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy., Banelli B; Tumor Epigenetics Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy., Morabito A; Tumor Epigenetics Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy., Pistillo MP; Tumor Epigenetics Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy., Croce E; Skin Cancer Unit, Medical Oncology 2, IRCCS Ospedale Policlinico San Martino, Genova, Italy.; Medical Oncology, Ospedale Santa Corona, 17027 Pietra Ligure, Savona, Italy., Queirolo P; Division of Melanoma Sarcoma and Rare Tumors, IRCCS European Institute of Oncology, Milan, Italy., Tanda ET; Skin Cancer Unit, Medical Oncology 2, IRCCS Ospedale Policlinico San Martino, Genova, Italy.; Department of Internal Medicine and Medical Specialties (DIMI), School of Medicine, University of Genoa, Genova, Italy., Raposio E; Department of Surgical Sciences and Integrated Diagnostics (DISC), Plastic Surgery Division, University of Genoa, Genova, Italy., Fontana V; Clinical Epidemiology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy., Spagnolo F; Skin Cancer Unit, Medical Oncology 2, IRCCS Ospedale Policlinico San Martino, Genova, Italy.; Department of Surgical Sciences and Integrated Diagnostics (DISC), Plastic Surgery Division, University of Genoa, Genova, Italy.

المصدر: Archives of dermatological research [Arch Dermatol Res] 2024 Jun 16; Vol. 316 (7), pp. 414. Date of Electronic Publication: 2024 Jun 16.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 8000462 Publication Model: Electronic Cited Medium: Internet ISSN: 1432-069X (Electronic) Linking ISSN: 03403696 NLM ISO Abbreviation: Arch Dermatol Res Subsets: MEDLINE

مواضيع طبية MeSH: Melanoma*/genetics , Programmed Cell Death 1 Receptor*/genetics , Polymorphism, Single Nucleotide* , Genetic Predisposition to Disease* , Gene Frequency* , Skin Neoplasms*/genetics , Skin Neoplasms*/pathology, Humans ; Female ; Male ; Middle Aged ; Aged ; Case-Control Studies ; Adult ; Genotype ; Immune Checkpoint Inhibitors/therapeutic use ; Alleles

المؤلفون: Zeng W; Department of Stomatology, The People's Hospital of Yichun City, Yichun, Jiangxi, 336028, China., Xu W; Department of Stomatology, The People's Hospital of Yichun City, Yichun, Jiangxi, 336028, China., Long W; Department of Stomatology, The Second People's Hospital of Yichun City, Yichun, Jiangxi, 336028, China. nemo9696@163.com.

المصدر: BMC cancer [BMC Cancer] 2024 Jun 15; Vol. 24 (1), pp. 738. Date of Electronic Publication: 2024 Jun 15.

نوع المنشور: Journal Article; Meta-Analysis

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 100967800 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2407 (Electronic) Linking ISSN: 14712407 NLM ISO Abbreviation: BMC Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Mouth Neoplasms*/genetics , Xeroderma Pigmentosum Group D Protein*/genetics , Polymorphism, Single Nucleotide* , Genetic Predisposition to Disease*, Humans ; Odds Ratio ; Alleles ; Asian People/genetics ; Risk Factors

المؤلفون: Wang C; Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China; Central Laboratory, Renmin Hospital of Wuhan University, Wuhan, China., Gao Y; Central Laboratory, Renmin Hospital of Wuhan University, Wuhan, China; Department of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan, China., Smerin D; Department of Neurosurgery, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA., Xiong X; Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China; Central Laboratory, Renmin Hospital of Wuhan University, Wuhan, China., Chen Z; Department of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, China. Electronic address: chzbiao@126.com., Gu L; Central Laboratory, Renmin Hospital of Wuhan University, Wuhan, China; Department of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan, China. Electronic address: gulijuan@whu.edu.cn.

المصدر: International immunopharmacology [Int Immunopharmacol] 2024 Jun 15; Vol. 134, pp. 112267. Date of Electronic Publication: 2024 May 17.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Science Country of Publication: Netherlands NLM ID: 100965259 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-1705 (Electronic) Linking ISSN: 15675769 NLM ISO Abbreviation: Int Immunopharmacol Subsets: MEDLINE

مواضيع طبية MeSH: Diabetes Mellitus, Type 2*/blood , Diabetes Mellitus, Type 2*/genetics , Uric Acid*/blood , Ischemic Stroke*/blood , Ischemic Stroke*/genetics , Mendelian Randomization Analysis* , Genetic Predisposition to Disease*, Humans ; Polymorphism, Single Nucleotide

المؤلفون: Huang X; Department of Neurology, Wenzhou Central Hospital & Dingli Clinical Institute of Wenzhou Medical University, Wenzhou, Zhejiang, PR China., Ye Q; Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China., Zhu Z; Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China., Chen Y; Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China., Xia N; Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China., Chen R; Department of Neurology, Wenzhou Central Hospital & Dingli Clinical Institute of Wenzhou Medical University, Wenzhou, Zhejiang, PR China., Geng W; Department of Anesthesiology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China; Wenzhou Key Laboratory of Perioperative Medicine, Wenzhou, Zhejiang, PR China. Electronic address: gengwujun@126.com., Ye Z; Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China; Wenzhou Key Laboratory of Perioperative Medicine, Wenzhou, Zhejiang, PR China. Electronic address: zusenye@163.com.

المصدر: Brain research [Brain Res] 2024 Jun 15; Vol. 1833, pp. 148867. Date of Electronic Publication: 2024 Mar 16.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier/North-Holland Biomedical Press Country of Publication: Netherlands NLM ID: 0045503 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-6240 (Electronic) Linking ISSN: 00068993 NLM ISO Abbreviation: Brain Res Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Single Nucleotide*/genetics , Stroke*/genetics , Genetic Predisposition to Disease*/genetics, Humans ; Male ; Female ; Aged ; Middle Aged ; Atherosclerosis/genetics ; Chromosomes, Human, Pair 3/genetics ; Risk Factors ; Genotype ; Intracranial Arteriosclerosis/genetics

المؤلفون: Zhao X; Department of Physical Education and Arts, Bengbu Medical College, Bengbu, China.; Graduate School, Adamson University, Manila, Philippines., Liu J; Physical Education Department, Bozhou University, Bozhou, China., Zhang L; Department of Physical Education and Arts, Bengbu Medical College, Bengbu, China., Ma C; Department of Physical Education and Arts, Bengbu Medical College, Bengbu, China., Liu Y; Department of Physical Education and Arts, Bengbu Medical College, Bengbu, China., Wen H; Department of Physical Education and Arts, Bengbu Medical College, Bengbu, China., Li CQ; Department of Physical Education and Arts, Bengbu Medical College, Bengbu, China.

المصدر: Medicine [Medicine (Baltimore)] 2024 Jun 14; Vol. 103 (24), pp. e38561.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN: 1536-5964 (Electronic) Linking ISSN: 00257974 NLM ISO Abbreviation: Medicine (Baltimore) Subsets: MEDLINE

مواضيع طبية MeSH: Mendelian Randomization Analysis* , Scoliosis*/genetics , Gastrointestinal Microbiome*/genetics , Genome-Wide Association Study* , Genetic Predisposition to Disease*, Humans ; Inflammation Mediators/metabolism ; Inflammation Mediators/blood