Searching for genetic determinants in the new millennium

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Items 901–1,000 of 1,000

1. A GENTLE INTRODUCTION TO SNP ANALYSIS: RESOURCES AND TOOLS
   James T. L. Mah, Kee‐Seng Chia · 2007 · Journal of Bioinformatics and Computational Biology
2. Genetic variation in immune function and susceptibility to human filariasis
   Eun Hwa Choi, Thomas B. Nutman, Stephen Jacob Chanock · 2003 · Expert Review of Molecular Diagnostics
3. Genetic isolates in Corsica (France): linkage disequilibrium extension analysis on the Xq13 region
   Veronica Latini, Gabriella Sole, Silvia Doratiotto, Daniela Poddie, Marc Memmi, Laurent Varesi, Giuseppe Vona, Antonio Cao, Maria Serafina Ristaldi · 2004 · European Journal of Human Genetics
4. Efficient SNP‐based tests of association for quantitative phenotypes using pooled DNA
   Joel S. Bader, Aruna T. Bansal, Pak Chung Sham · 2001 · GeneScreen
5. Commentary: Understanding sources of complexity in chronic diseases—the importance of integration of genetics and epidemiology
   Kathleen Ries Merikangas, Nancy C. P. Low, John Hardy · 2006 · International Journal of Epidemiology
6. Celiac disease: moving from genetic associations to causal variants
   Barbara Hrdličková, Harm-Jan Westra, Lude Franke, Cisca Wijmenga · 2011 · Clinical Genetics
7. Designs for Linkage Analysis and Association Studies of Complex Diseases
   Yuehua Cui, Gengxin Li, Shaoyu Li, Rongling Wu · 2009 · Methods in molecular biology
8. Molecular and functional genetics of hepatocellular carcinoma
   Irene Oi‐Lin Ng · 2009 · Frontiers in Bioscience-Scholar
9. An audit of the statistics and the comparison with the parameter in the population
   Mohamad Adam Bujang, Nadiah Sa’at, A. Reena Joys, Mariana Mohamad Ali · 2015 · AIP conference proceedings
10. Ethnicity affects the distribution of δ-aminolevulinic acid dehydratase (ALAD) genetic variants
    Marcelo Freitas Montenegro, Fernando Barbosa, Valéria C. Sandrim, Raquel F. Gerlach, José Eduardo Tanus-Santos · 2006 · Clinica Chimica Acta
11. Association study of the thrombomodulin −33G>A polymorphism with coronary artery disease and myocardial infarction in Chinese Han population
    Jiangong Zhao, Xiaoyang Zhou, Jianfeng Huang, Jianhong Chen, Dongfeng Gu · 2004 · International Journal of Cardiology
12. Genetic linkage findings for DSM‐IV nicotine withdrawal in two populations
    Michele L. Pergadia, Arpana Agrawal A, Anu Loukola, Grant W. Montgomery, Ulla Broms, Scott F. Saccone, Jen Chin C. Wang, Alexandre A. Todorov, Kauko V Heikkila, Dixie J. Statham et al. · 2009 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
13. Genome-Wide Association Studies: Progress in Identifying Genetic Biomarkers in Common, Complex Diseases
    Stephen Francis Kingsmore, Ingrid E. Lindquist, Joann Mudge, William Dale Beavis · 2007 · Biomarker Insights
14. Population Screening of Single-Nucleotide Polymorphisms Exemplified by Analysis of 8000 Alleles
    Per Olaf Ekstrøm, Jens Bjørheim, Gustav Gaudernack, Karl-Erik Giercksky · 2002 · SLAS DISCOVERY
15. Association between the adiponectin promoter rs266729 gene variant and oxidative stress in patients with diabetes mellitus
    Sarah L. Prior, David R. Gable, Jackie A. Cooper, S. Bain, Steven J. Hurel, Steve Eric Humphries, Jeffrey Wayne Stephens · 2009 · European Heart Journal
16. Genetic epidemiology. Approaches to the genetic analysis of rheumatoid arthritis.
    Sally John, Jane Worthington · 2001 · Arthritis Research
17. Population differences in the International Multi‐Centre ADHD Gene Project
    Benjamin M. Neale, Pak Chung Sham, Shaun Purcell, Tobias Banaschewski, Jan K. Buitelaar, Barbara Franke, Edmund J. S. Sonuga-Barke, Richard P. Ebstein, Jacques Eisenberg, Aisling Mulligan et al. · 2007 · Genetic Epidemiology
18. From mouse to human: Fine mapping of quantitative trait loci in a model organism
    Mary Sara McPeek · 2000 · Proceedings of the National Academy of Sciences
19. The Genetics of Type 2 Diabetes
    Cecilia M. Lindgren, Joel N. Hirschhorn · 2001 · The Endocrinologist
20. Gene-Environment Interrelations in Prostate Cancer
    Richard B. Hayes · 2001 · Epidemiologic Reviews
21. Rethinking genetic strategies to study complex diseases
    Anthony J. Brookes · 2001 · Trends in Molecular Medicine
22. Candidate‐gene association studies with pedigree data: Controlling for environmental covariates
    Susan L. Slager, Daniel J. Schaid, Lan Wang, Stephen N. Thibodeau · 2003 · Genetic Epidemiology
23. Identification of 96 single nucleotide polymorphisms in eight genes involved in iron metabolism: efficiency of bioinformatic extraction compared with a systematic sequencing approach
    Véronique Douabin-Gicquel, Nicolas Soriano, Hélène Ferran, F Wojcik, Elisabeth Palierne, Sara Tamim, Thomas Jovelin, Andrew Tristan McKie, Jean‐Yves Le Gall, Véronique David et al. · 2001 · Human Genetics
24. Nature and nurture
    Kenneth F. Schaffner · 2001 · Current Opinion in Psychiatry
25. Insights into protein function through large-scale computational analysis of sequence and structure
    Malcolm Weir, Mark B. Swindells, John P. Overington · 2001 · Trends in biotechnology
26. Mission: not impossible? Candidate gene studies in child psychiatric disorders
    David Andrew Collier, Sarah R Curran, Philip J. Asherson · 2000 · Molecular Psychiatry
27. Genetic architecture reconciles linkage and association studies of complex traits
    Julia Sidorenko, Baptiste Couvy‐Duchesne, Kathryn E. Kemper, Gunn-Helen Moen, Laxmi Bhatta, Bjørn Olav Åsvold, Reedik Mägi, Alireza Ani, Rujia Wang, Ilja Maria Nolte et al. · 2024 · Nature Genetics
28. Do genetic polymorphisms affect susceptibility to periodontal disease? A literature review
    MO Uslu, VE Toy · 2019 · Nigerian Journal of Clinical Practice
29. Progressing From Risk Factors to Omics
    Peter W.F. Wilson · 2008 · Circulation Cardiovascular Genetics
30. Aberrant Cosmc genes result in Tn antigen expression in human colorectal carcinoma cell line HT-29.
    Xiaofeng Yu, Zhenzhen Du, Xuhong Sun, Chuanqin Shi, Huaixiang Zhang, Tao Hu · 2015 · PubMed Central
31. Decision Tree Induction in High Dimensional, Hierarchically Distributed Databases
    Amir Bar-Or, Assaf Schuster, Ran Wolff, Daniel Keren · 2005 · SIAM International Conference on Data Mining
32. Polymorphism analysis of the upstream region of the human N-methyl-d-aspartate receptor subunit NR1 gene (GRIN1): implications for schizophrenia
    Ayako Tani, Rumiko Kikuta, Kanako Itoh, Akiko Joo, Hiroki Shibata, Hideaki Ninomiya, Nobutada Tashiro, Yasuyuki Fukumaki · 2002 · Schizophrenia Research
33. Power of non‐parametric linkage analysis in mapping genes contributing to human longevity in long‐lived sib‐pairs
    Qihua Tan, Jinghua Zhao, Ivan A. Iachine, Jacob Hjelmborg, Werner Vach, James W. Vaupel, Kaare Christensen, Torben Arvid Kruse · 2004 · Genetic Epidemiology
34. Genetic determinants of the stress response in cardiovascular disease
    Pavel Hamet, Johanne Tremblay · 2002 · Metabolism
35. Polymorphisms in Immunoregulatory Genes
    Ann K. Daly, Christopher Paul Day, Peter T. Donaldson · 2002 · American Journal of PharmacoGenomics
36. Genetic Variation and Exposure Related Risk Estimation: Will Toxicology Enter a New Era? DNA Repair and Cancer as a Paradigm
    Harvey W. Mohrenweiser · 2004 · Toxicologic Pathology
37. The relationship between polymorphisms at 17 gene sites and hypertension among the Aboriginal Tibetan people.
    Kui Li, Yu Liang, Yin Sun, Ling Xia Zhang, Xin Yi, Yong Chen, Gu Sang LA Mu, Jian Wang · 2012 · PubMed
38. Metabonomics and population studies: age-related amino acids excretion and inferring networks through the study of urine samples in two Italian isolated populations
    Pio D’Adamo, Sheila Ulivi, Amerigo Beneduci, Gabriele Pontoni, Giovambattista Capasso, Carmela Lanzara, Gilberto Andrighetto, Uroš Hladnik, Virginia Nunes, Manuel Palacı́n et al. · 2008 · Amino Acids
39. A polymorphism in CALHM1 is associated with temporal lobe epilepsy
    Ruijuan Lv, Jinsheng He, Yuan-Hui Fu, Xiaoqiu Shao, Liwen Wu, Qiang Lu, Liri Jin, Hui Liu · 2011 · Epilepsy & Behavior
40. Interactions Between Life Stress Factors and Carrying the APOE4 Allele Adversely Impact Self-reported Health in Old Adults
    Yi Zeng, Claude L. Hughes, Megan A. Lewis, J. Li, Fengyu Zhang · 2011 · The Journals of Gerontology Series A
41. A Microfluidic-Based SNP Genotyping Method for Hereditary Hearing-Loss Detection
    Ying Lu, Shan Chen, Li Wei, Lanhua Sun, Houming Liu, Youchun Xu · 2019 · Analytical Chemistry
42. Ethical Challenges of Genomic Epidemiology in Developing Countries
    Dave A. Chokshi, Dominic P. Kwiatkowski · 2005 · Genomics Society and Policy
43. DNA pooling: a comprehensive, multi‐stage association analysis of ACSL6 and SIRT5 polymorphisms in schizophrenia
    Kodavali V. Chowdari, Abbegail Northup, Lora Pless, Joel A. Wood, Y. H. Joo, Károly Mirnics, David A. Lewis, Pat R. Levitt, Silviu‐Alin Bacanu, Vishwajit Laxmikant Nimgaonkar · 2006 · Genes Brain & Behavior
44. Two-stage association tests for genome-wide association studies based on family data with arbitrary family structure
    Tao Feng, Shuanglin Zhang, Qiuying Sha · 2007 · European Journal of Human Genetics
45. Optimal Two‐Stage Design for Case‐Control Association Analysis Incorporating Genotyping Errors
    Yijun Zuo, G. Zou, Jian Wang, Hongyu Zhao, Hua Liang · 2008 · Annals of Human Genetics
46. Improving the power of association tests for quantitative traits in family studies
    Guoqing Diao, Dan Yu Lin · 2006 · Genetic Epidemiology
47. Multiple sclerosis as a polygenic disease: An update
    Olga O. Favorova, О. Г. Кулакова, А. Н. Бойко · 2010 · Russian Journal of Genetics
48. Positional Cloning of Ncf1– a Piece in the Puzzle of Arthritis Genetics
    Peter Olofsson, Rikard Holmdahl · 2003 · Scandinavian Journal of Immunology
49. Relationships between familial risks of cancer and the effects of heritable genes and their SNP variants
    Kari Hemminki, Justo Lorenzo Bermejo · 2005 · Mutation research. Fundamental and molecular mechanisms of mutagenesis
50. Nonparametric Disequilibrium Mapping of Functional Sites Using Haplotypes of Multiple Tightly Linked Single-Nucleotide Polymorphism Markers
    Rong Cheng, Jennie Z. Ma, Fred A. Wright, Shili Lin, Xin Gao, Daolong Wang, Robert C. Elston, Ming D. Li · 2003 · Genetics
51. Meta-analysis for linkage to asthma and atopy in the chromosome 5q31-33 candidate region
    Lyle John Palmer · 2001 · Human Molecular Genetics
52. The comparative patterns of linkade disequilibrium in European populations and its implication for genetic association studies
    Elin Lõhmussaar · 2006 · DSpace repository (University of Tartu)
53. A comprehensive meta-analysis of genetic associations between five key SNPs and colorectal cancer risk
    Hong Yi, Guoying Wu, Wei Li, Dahai Liu, Kan He · 2016 · Oncotarget
54. Association mapping and marker development of the candidate genes (1 → 3),(1 → 4)-β-d-Glucan-4-glucanohydrolase and (1 → 4)-β-Xylan-endohydrolase 1 for malting quality in barley
    Inge E. Matthies, Stephan F. Weise, Jutta Förster, Marion S. Röder · 2009 · Euphytica
55. Reliable and Fast Estimation of Recombination Rates by Convergence Diagnosis and Parallel Markov Chain Monte Carlo
    Jing Guo, Ritika Jain, Peng Yang, Rui Fan, Chee Keong Kwoh, Jie Zheng · 2013 · IEEE Transactions on Computational Biology and Bioinformatics
56. Association of genetic variants of the vitamin D receptor (VDR) gene (Fok-I, Taq-I and Bsm-I) with susceptibility of benign prostatic hyperplasia in a North Indian population.
    Parmeet Kaur Manchanda, Rituraj Konwar, V Lakshma Nayak, Vishwajeet Singh, Hemant Kumar Bid · 2010 · PubMed
57. Gender-specific association between the kininogen 1 gene variants and essential hypertension in Chinese Han population
    Weiyan Zhao, Yaping Wang, Laiyuan Wang, Xiangfeng Lu, Wei Yang, Jianfeng Huang, Shufeng Chen, Dongfeng Gu · 2009 · Journal of Hypertension
58. Racial differences and the genetics of hypertension
    Richard Cooper, Xiaofeng Zhu · 2001 · Current Hypertension Reports
59. The genetics of atrial fibrillation
    Mohamad Khaled Sabeh, Calum A. MacRae · 2010 · Current Opinion in Cardiology
60. TNF-α and IFN-γ gene variation and genetic susceptibility to type 1 diabetes and its microangiopathic complications
    Javad Tavakkoly‐Bazzaz, Mahsa Mohammad Amoli, Zahra Taheri, Bagher A. Larijani, Vera Pravica, Ian V. Hutchinson · 2014 · Journal of Diabetes & Metabolic Disorders
61. Novel SNPs of the mannan-binding lectin 2 gene and their association with production traits in Chinese Holsteins
    Zihan Zhao, C.F. Wang, Q.L. Li, Z.H. Ju, J.M. Huang, Jianbin Li, Juming Zhong, Jing Zhang · 2012 · Genetics and Molecular Research
62. Allele, genotype, and composite genotype effects of IL-1A +4845 and IL-1B +3954 polymorphisms for chronic periodontitis in an Indian population
    R. Gayathri, Abdul Vahab Saadi, KMahalinga Bhat, Subraya G Bhat, Kapaettu Satyamoorthy · 2011 · Indian Journal of Dental Research
63. GENETICS OF SCHIZOPHRENIA
    Mohd Razali Salleh · 1966 · The Lancet
64. Genómica de la regulación del peso corporal: mecanismos moleculares que predisponen a la obesidad
    Raúl A. Bastarrachea, Shelley A. Cole, Anthony Gean Comuzzie · 2004 · Medicina Clínica
65. Analytical Correction for Multiple Testing in Admixture Mapping
    Qiuying Sha, Xihuan Zhang, Xiaofeng Zhu, Shuanglin Zhang · 2006 · Human Heredity
66. IGF1, growth pathway polymorphisms and schizophrenia: A pooling study
    David Gunnell, Sarah Jane Lewis, J. Wilkinson, L. Georgieva, G. Smith Davey, Ian N.M. Day, Jeff M.P. Holly, Michael C. O’Donovan, Michael John Owen, George Kirov et al. · 2006 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
67. Detecting AIDS restriction genes: From candidate genes to genome-wide association discovery
    Holli B. Hutcheson, James A. Lautenberger, George W. Nelson, Joan U. Pontius, Bailey D. Kessing, C.A. Winkler, Michael W. Smith, Randall C. Johnson, R. Stephens, John Phair et al. · 2008 · Vaccine
68. Molecular Genetics and g
    Robert J. Plomin · 2003 · Elsevier eBooks
69. Post-genomic nematode parasitology
    Warwick N. Grant, Mark Viney · 2001 · International Journal for Parasitology
70. Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic Epidemiology
    Aihua Li, David Meyre · 2014 · Current Psychiatry Reviews
71. Interpretation of the role of germline and somatic non-coding mutations in cancer: expression and chromatin conformation informed analysis
    Michael Pudjihartono, Jo Kate Perry, Cristin Gregor Print, Justin Martin O'Sullivan, William S. Schierding · 2022 · Clinical Epigenetics
72. Genome‐Wide Family‐Based Linkage Analysis of Exome Chip Variants and Cardiometabolic Risk
    Jacklyn N. Hellwege, Nicholette D. Palmer, Laura M. Raffield, Maggie C.Y. Ng, Gregory A. Hawkins, Jirong Long, Carlos Lorenzo, Jill M. Norris, Yii‐Der Ida Chen, Elizabeth K. Speliotes et al. · 2014 · Genetic Epidemiology
73. The genetics of reading disability
    Tracey L. Petryshen, David L. Pauls · 2009 · Current Psychiatry Reports
74. The ‘Missing Heritability’ of Common Disorders: Should Health Researchers Care?
    Claudia Chaufan, Jay Joseph · 2013 · International Journal of Health Services
75. Exome sequencing in a family segregating for celiac disease
    AM Szperl, Isis Ricaño-Ponce, JK Li, Patrick Deelen, Alexandros Kanterakis, Vincent Plagnol, Freerk van Dijk, Harm-Jan Westra, Gosia Trynka, Chris Jacob Johan Mulder et al. · 2011 · Clinical Genetics
76. Replication and Heritability of Prostate Cancer Risk Variants: Impact of Population-Specific Factors
    Victor Virlogeux, Rebecca E. Graff, Thomas J. Hoffmann, John S. Witte · 2015 · Cancer Epidemiology Biomarkers & Prevention
77. Machine learning analysis of exome trios to contrast the genomic architecture of autism and schizophrenia
    Sameer Sardaar, Bill Qi, Alexandre Dionne‐Laporte, Guy Armand Rouleau, Reihaneh Rabbany, Yannis J Trakadis · 2020 · BMC Psychiatry
78. Social-Emotional Development Through a Behavior Genetics Lens
    Lisabeth Fisher DiLalla, Paula Y. Mullineaux, S. J. W. Biebl · 2012 · Advances in child development and behavior
79. Principles in genetic risk assessment
    Pedro Viana Baptista · 2005 · Therapeutics and Clinical Risk Management
80. An ensemble learning approach jointly modeling main and interaction effects in genetic association studies
    Zhaogong Zhang, Shuanglin Zhang, Man-Yu Wong, Nicholas J. Wareham, Qiuying Sha · 2008 · Genetic Epidemiology
81. Associations betweenDRDs and schizophrenia in a Korean population: multi-stage association analyses
    Kyu Young Lee, Eun-Jeong Joo, Yong Ick Ji, Duk‐Hwan Kim, Joobae Park, In‐Won Chung, Sang-Ick Lee, Yeon Ho Joo, Yong Min Ahn, Joo Yun Song et al. · 2011 · Experimental & Molecular Medicine
82. Germline Genetic Profiling in Prostate Cancer: Latest Developments and Potential Clinical Applications
    Mahbubl Ahmed, Rosalind A. Eeles · 2015 · Future Science OA
83. Basic Concepts of Inflammation and its Role in Carcinogenesis
    Stephen G. Maher, John Vincent Reynolds · 2011 · Recent results in cancer research/Recent Results in Cancer Research
84. The genetics of cardiovascular disease
    Christian Delles, Martin McBride, Sandosh Padmanabhan, Anna F. Dominiczak · 2008 · Trends in Endocrinology and Metabolism
85. Genetic association analysis of myocardial infarction with thrombospondin-1 N700S variant in a Chinese population
    Xiaoyang Zhou, Jianfeng Huang, Jianhong Chen, Jiangong Zhao, Dongliang Ge, Wenjie Yang, Dongfeng Gu · 2004 · Thrombosis Research
86. Haplotype Structure and Ethnic-specific Allele Frequencies at the OCTN Locus: Implications for the Genetics of Crohnʼs Disease
    Thomas Jacob Urban, Kathleen M. Giacomini, NEIL J. RISCH · 2005 · Inflammatory Bowel Diseases
87. Is Variation in the GABA(B) Receptor 1 Gene Associated with Temporal Lobe Epilepsy?
    Nigel CK Tan, Sarah E. Heron, Ingrid Eileen Scheffer, Samuel Frank Berkovic, John C. Mulley · 2005 · Epilepsia
88. High-Throughput Single-Nucleotide Polymorphism Genotyping by Fluorescent Competitive Allele-Specific Polymerase Chain Reaction (SNiPTag)
    Joseph L. McClay, Karen Sugden, Helga G. Koch, Susumi Higuchi, Ian Craig · 2002 · Analytical Biochemistry
89. Searching for genetic determinants of human aging and longevity: opportunities and challenges
    Jan Vijg, Nathalie J. van Orsouw · 2002 · Mechanisms of Ageing and Development
90. Microarrays and genetic epidemiology: A multipurpose tool for a multifaceted field
    Dennise D. Dalma‐Weiszhausz, Marina Chicurel, T Gingeras · 2002 · Genetic Epidemiology
91. Re‐Screening serotonin receptors for genetic variants identifies population and molecular genetic complexity
    Charles E. Glatt, Maricel Tampilic, Carroll Christie, Joe DeYoung, Nelson B. Freimer · 2003 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
92. Sequence variants of the HTR3A gene contribute to the genetic prediction of postoperative nausea in Taiwan
    Joy Lin, Yi-Mei, Hsu, Cheng-Da, Hsieh, Hsiao-Yen, Tseng, Chia-Chih Alex, Sun, H Sunny · 2014 · Journal of Human Genetics
93. Genetic variants and the risk for invasive mould disease in immunocompromised hematology patients
    Walter J. F. M. van der Velden, Nicole M. A. Blijlevens, J. Peter Donnelly · 2011 · Current Opinion in Infectious Diseases
94. Genetic Basis of Nondiabetic End-Stage Renal Disease
    Barry I. Freedman, Rulan Savita Parekh, W.H. Linda Kao · 2010 · Seminars in Nephrology
95. Acyl-CoA synthetase long-chain family member 6 is associated with premature ovarian failure
    HyunJun Kang, Seung Ku Lee, Min Ho Kim, Hyejeong Choi, Sook‐Hwan Lee, KyuBum Kwack · 2008 · Fertility and Sterility
96. Statistical distributions of test statistics used for quantitative trait association mapping in structured populations
    Simon Teyssèdre, Jean-Michel Elsen, Anne Ricard · 2012 · Genetics Selection Evolution
97. Genetic Basis of Autism
    Elena Bonora, Anthony P. Monaco, Janine A. Lamb, Anthony J. Bailey, Gabrielle Barnby · 2006 · CRC Press eBooks
98. Case-control study on the association between the GATA2 gene and premature myocardial infarction in the Iranian population
    Peyman Izadpanah, Ehsan Khabbzi, Saiedeh Erfanian, Simin Jafaripour, Mohammad Shojaie · 2019 · Herz
99. The devil is in the DNA
    Stephen Jacob Chanock, Gilles D. Thomas · 2007 · Nature Genetics
100. Expression of host defense scavenger receptors in spondylarthropathy
     McBeth · 2001 · Pure Amsterdam UMC