المؤلفون: Zhang N; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China., Huang D; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China., Jiang G; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China., Chen S; Department of Urology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200080, China., Ruan X; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China., Chen H; School of Public Health Shenzhen, Sun Yat-sen University, Guangzhou, 510006, China., Huang J; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China., Liu A; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China., Zhang W; Department of Urology, Changhai Hospital, Second Military Medical University, Shanghai, 200433, China., Lin X; Department of Urology, Huashan Hospital, Fudan University, Shanghai, 200040, China., Wu Y; Department of Urology, Huashan Hospital, Fudan University, Shanghai, 200040, China., Zhang Q; Biocenter Oulu, Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, 90014, Finland., Li J; Department of Bioinformatics, Center for Translational Medicine, Second Military Medical University, Shanghai, 200433, China., Tsu JH; Division of Urology, Department of Surgery, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China., Wei GH; Biocenter Oulu, Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, 90014, Finland.; MOE Key Laboratory of Metabolism and Molecular Medicine & Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, and Fudan University Shanghai Cancer Center, Shanghai Medical College of Fudan University, Shanghai, 200032, China., Na R; Division of Urology, Department of Surgery, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.

المصدر: Advanced science (Weinheim, Baden-Wurttemberg, Germany) [Adv Sci (Weinh)] 2022 Aug; Vol. 9 (23), pp. e2201420. Date of Electronic Publication: 2022 Jun 17.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: WILEY-VCH Country of Publication: Germany NLM ID: 101664569 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2198-3844 (Electronic) Linking ISSN: 21983844 NLM ISO Abbreviation: Adv Sci (Weinh) Subsets: MEDLINE

مواضيع طبية MeSH: 3' Untranslated Regions*/genetics , Homeodomain Proteins*/genetics , MicroRNAs*/genetics , Polymorphism, Single Nucleotide*/genetics , Prostatic Neoplasms*/genetics , Transcription Factors*/genetics, China ; Genome-Wide Association Study ; Humans ; Male

المؤلفون: Zhang C; Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, State Key Laboratory of Oncogenes and Related Genes, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China., Zheng T; Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, State Key Laboratory of Oncogenes and Related Genes, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China., Ma Q; Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, State Key Laboratory of Oncogenes and Related Genes, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China., Yang L; Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, State Key Laboratory of Oncogenes and Related Genes, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China., Zhang M; Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, State Key Laboratory of Oncogenes and Related Genes, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China., Wang J; Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, State Key Laboratory of Oncogenes and Related Genes, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China., Teng X; Department of Laboratory Medicine, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, 201306, China., Miao Y; Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, State Key Laboratory of Oncogenes and Related Genes, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China., Lin HC; Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, State Key Laboratory of Oncogenes and Related Genes, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China., Yang Y; Department of Thoracic Surgery, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, 200433, China., Han D; Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, State Key Laboratory of Oncogenes and Related Genes, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, China.

المصدر: Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2022 Apr 04; Vol. 61 (15), pp. e202117658. Date of Electronic Publication: 2022 Feb 16.

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

بيانات الدورية: Publisher: Wiley-VCH Country of Publication: Germany NLM ID: 0370543 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1521-3773 (Electronic) Linking ISSN: 14337851 NLM ISO Abbreviation: Angew Chem Int Ed Engl Subsets: MEDLINE

مواضيع طبية MeSH: Computers, Molecular* , Polymorphism, Single Nucleotide*, DNA/genetics ; Genotype ; Nucleotides ; Sequence Analysis, DNA

المؤلفون: Yang H; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine Northwestern University, Chicago, IL, USA.; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.; Obstetrics and Gynecology Hospital, Institute of Reproduction and Development, Fudan University, Shanghai, China., Zhang H; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA.; Department of Hematology/Oncology, Guangzhou Women and Children's Medical Center, Guangzhou, China.; Department of Hematology/Oncology, Shanghai Children's Medical Center, Shanghai, China., Luan Y; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine Northwestern University, Chicago, IL, USA., Liu T; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine Northwestern University, Chicago, IL, USA., Yang W; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA., Roberts KG; Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA., Qian MX; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA., Zhang B; Bioinformatics and Genomics Program, The Pennsylvania State University, University Park, PA, USA., Yang W; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA., Perez-Andreu V; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA.; Internal Medicine Department, MountainView Hospital, University of Reno, Las Vegas, NV, USA., Xu J; Department of Biochemistry and Molecular Biology, Penn State School of Medicine, Hershey, PA, USA., Iyyanki S; Department of Biochemistry and Molecular Biology, Penn State School of Medicine, Hershey, PA, USA., Kuang D; Department of Computer and Information Science, University of Pennsylvania, Philadelphia, PA, USA., Stasiak LA; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine Northwestern University, Chicago, IL, USA., Reshmi SC; Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH, USA.; Department of Pediatrics, Ohio State University School of Medicine, Columbus, OH, USA., Gastier-Foster J; Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH, USA.; Department of Pediatrics, Ohio State University School of Medicine, Columbus, OH, USA., Smith C; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA., Pui CH; Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA., Evans WE; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA., Hunger SP; Division of Oncology and the Center for Childhood Cancer Research, Children's Hospital of Philadelphia and the Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA., Platanias LC; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA., Relling MV; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA., Mullighan CG; Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA., Loh ML; Department of Pediatrics, Benioff Children's Hospital and the Helen Diller Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA, USA., Yue F; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine Northwestern University, Chicago, IL, USA. yue@northwestern.edu.; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA. yue@northwestern.edu., Yang JJ; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA. jun.yang@stjude.org.

المصدر: Nature genetics [Nat Genet] 2022 Feb; Vol. 54 (2), pp. 170-179. Date of Electronic Publication: 2022 Feb 03.

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

بيانات الدورية: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease* , Polymorphism, Single Nucleotide*, Chromatin/*chemistry , GATA3 Transcription Factor/*genetics , Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics, Child ; Chromatin/metabolism ; Enhancer Elements, Genetic ; Female ; GATA3 Transcription Factor/metabolism ; Genome, Human ; Humans ; Janus Kinases/metabolism ; Male ; Oncogenes ; Philadelphia Chromosome ; Protein Binding ; Receptors, Cytokine/genetics ; Receptors, Cytokine/metabolism ; STAT Transcription Factors/metabolism ; Signal Transduction ; Up-Regulation

المؤلفون: Huang D; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China., Ruan X; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China., Wu Y; Department of Urology, Huashan Hospital, Fudan University, Shanghai, China., Lin X; Department of Urology, Huashan Hospital, Fudan University, Shanghai, China., Huang J; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China., Ye D; Department of Urology, Shanghai Cancer Center, Fudan University, Shanghai, China., Gao Y; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China., Ding Q; Shanghai Medical College, Fudan University, Shanghai, China., Xu D; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China., Na R; Department of Urology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

المصدر: The Prostate [Prostate] 2021 Sep; Vol. 81 (13), pp. 971-982. Date of Electronic Publication: 2021 Jul 12.

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

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8101368 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0045 (Electronic) Linking ISSN: 02704137 NLM ISO Abbreviation: Prostate Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 19* , Polymorphism, Single Nucleotide*, Prostate-Specific Antigen/*blood , Prostatic Neoplasms/*genetics, Humans ; Male ; Prognosis ; Prospective Studies ; Prostatic Neoplasms/blood ; Prostatic Neoplasms/pathology

المؤلفون: Pan W; Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China. panweihua@caas.cn., Gong D; Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China., Sun D; Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China., Luo H; Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China.

المصدر: Scientific reports [Sci Rep] 2021 Mar 23; Vol. 11 (1), pp. 6609. Date of Electronic Publication: 2021 Mar 23.

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: Polymorphism, Single Nucleotide* , Software*, Genome-Wide Association Study/*methods , Neoplasms/*genetics, Genome, Human ; Humans ; K562 Cells

المؤلفون: Li W; Department of Pediatric Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China., Hua RX; Department of Oncology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China., Wang M; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China., Zhang D; Department of Pediatric Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China., Zhu J; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.; Department of Clinical Laboratory, Biobank, Harbin Medical University Cancer Hospital, Harbin, China., Zhang S; Department of Pediatric Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China., Yang Y; Department of Pediatric Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China., Cheng J; Department of Pediatric Surgery, the Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China., Zhou H; Department of Hematology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China., Zhang J; Department of Pediatric Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China., He J; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.

المصدر: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2021 Feb; Vol. 9 (2), pp. e1584. Date of Electronic Publication: 2021 Jan 05.

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

بيانات الدورية: Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2324-9269 (Electronic) Linking ISSN: 23249269 NLM ISO Abbreviation: Mol Genet Genomic Med Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Single Nucleotide*, RNA, Long Noncoding/*genetics , Wilms Tumor/*genetics, Child, Preschool ; China ; Female ; Genes, Modifier ; Humans ; Infant ; Male

المؤلفون: Zhao J; Department of Reproductive Medicine, Lianyungang Maternal and Child Health Hospital, NO.669 Qindongmen Road, Lianyungang, 222001, Jiangsu Province, China., Li D; Department of Vascular Surgery, the First People's Hospital of Lianyungang, NO.182 North Tongguan Road, Lianyungang, Jiangsu Province, 222002, China., Tang H; Department of Reproductive Medicine, Lianyungang Maternal and Child Health Hospital, NO.669 Qindongmen Road, Lianyungang, 222001, Jiangsu Province, China., Tang L; Department of Reproductive Medicine, Lianyungang Maternal and Child Health Hospital, NO.669 Qindongmen Road, Lianyungang, 222001, Jiangsu Province, China. 540660190@qq.com.

المصدر: Reproductive biology and endocrinology : RB&E [Reprod Biol Endocrinol] 2020 Mar 09; Vol. 18 (1), pp. 18. Date of Electronic Publication: 2020 Mar 09.

نوع المنشور: Journal Article; Meta-Analysis; Review

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101153627 Publication Model: Electronic Cited Medium: Internet ISSN: 1477-7827 (Electronic) Linking ISSN: 14777827 NLM ISO Abbreviation: Reprod Biol Endocrinol Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Single Nucleotide*, Genetic Predisposition to Disease/*genetics , Polycystic Ovary Syndrome/*genetics , Vascular Endothelial Growth Factor A/*genetics, Asian People/genetics ; Case-Control Studies ; Female ; Genetic Predisposition to Disease/ethnology ; Humans ; Polycystic Ovary Syndrome/ethnology ; Risk Factors ; White People/genetics

المؤلفون: Weng Y; Department of Clinical Laboratory, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China., Wang D; Department of Surgical Oncology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China. Electronic address: wangda0618@zju.edu.cn., Bai R; Department of Public Health, Zhejiang University School of Medicine, Hangzhou, China. Electronic address: rpbai@zju.edu.cn.

المصدر: Gene [Gene] 2020 Feb 05; Vol. 726, pp. 144173. Date of Electronic Publication: 2019 Oct 26.

نوع المنشور: Letter; Meta-Analysis

بيانات الدورية: Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0038 (Electronic) Linking ISSN: 03781119 NLM ISO Abbreviation: Gene Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease/*genetics , Polymorphism, Single Nucleotide/*genetics , Stomach Neoplasms/*etiology , Stomach Neoplasms/*genetics, Asian People/genetics ; Case-Control Studies ; Genotype ; Humans ; MicroRNAs/genetics ; Risk Factors ; White People/genetics

المؤلفون: Wei W; Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, China., You Z; Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, China., Sun S; Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, China., Wang Y; Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, China., Zhang X; Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, China., Pang D; Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, China.; North China Translational Medicine Research and Cooperation Center (NTMRC), Harbin, China., Jiang Y; Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, China.

المصدر: Molecular carcinogenesis [Mol Carcinog] 2018 Aug; Vol. 57 (8), pp. 988-996. Date of Electronic Publication: 2018 Apr 16.

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

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8811105 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-2744 (Electronic) Linking ISSN: 08991987 NLM ISO Abbreviation: Mol Carcinog Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Single Nucleotide*, Breast Neoplasms/*genetics , Receptor, Fibroblast Growth Factor, Type 4/*genetics, Adult ; Breast Neoplasms/diagnosis ; Female ; Genetic Predisposition to Disease ; Humans ; Kaplan-Meier Estimate ; Middle Aged ; Prognosis ; Up-Regulation

المؤلفون: Chen D; a Department of Ophthalmology, Wuhan Hospital of Traditional Chinese Medicine , Wuhan, China., Wang J; b Department of Ophthalmology , Affiliated Wuxi Hospital of Nanjing China Traditional Chinese Medicine , Wuxi, China., Dan Z; b Department of Ophthalmology , Affiliated Wuxi Hospital of Nanjing China Traditional Chinese Medicine , Wuxi, China., Shen X; b Department of Ophthalmology , Affiliated Wuxi Hospital of Nanjing China Traditional Chinese Medicine , Wuxi, China., Ci D; b Department of Ophthalmology , Affiliated Wuxi Hospital of Nanjing China Traditional Chinese Medicine , Wuxi, China.

المصدر: Ophthalmic genetics [Ophthalmic Genet] 2018 Apr; Vol. 39 (2), pp. 200-207. Date of Electronic Publication: 2017 Nov 28.

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

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1744-5094 (Electronic) Linking ISSN: 13816810 NLM ISO Abbreviation: Ophthalmic Genet Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Single Nucleotide*, Diabetic Retinopathy/*genetics , Ethnicity/*genetics , Methylenetetrahydrofolate Reductase (NADPH2)/*genetics, Asian People/genetics ; Case-Control Studies ; Diabetic Retinopathy/ethnology ; Gene Frequency ; Genetic Predisposition to Disease ; Humans ; Odds Ratio