Analysis of Human Genetic Linkage

Cited by (755)

Items 201–300 of 755

1. Biethnic Comparisons of Autosomal Genomic Scan for Loci Linked to Plasma Adiponectin in Populations of Chinese and Japanese Origin
   Lee‐Ming Chuang, Yen‐Feng Chiu, Wayne Huey‐Herng Sheu, Yi‐Jen Hung, Low-Tone Ho, John Grove, Beatriz L. Rodríguez, Thomas Quertermous, Yii‐Der Ida Chen, Chao Agnes Hsiung et al. · 2004 · The Journal of Clinical Endocrinology & Metabolism
2. Localization of multiple pleiotropic genes for lipoprotein metabolism in baboons
   David L. Rainwater, Laura A. Cox, Jeffrey Rogers · 2009 · Journal of Lipid Research
3. Performance of linkage analysis under misclassification error when the genetic model is unknown
   Maria M. Martinez, Myriam Khlat, Marion Leboyer · 1989 · Genetic Epidemiology
4. Parametric and Nonparametric Linkage Analysis
   Joan E. Bailey‐Wilson · 2018 · Encyclopedia of Life Sciences
5. TDT-HET: A new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data
   Douglas Londoño, Steven G. Buyske, Stephen J. Finch · 2012 · BMC Bioinformatics
6. Contrasting Methods of Quantifying Fine Structure of Human Recombination
   Andrew G. Clark, Xu Wang, Tara Cox Matise · 2010 · Annual Review of Genomics and Human Genetics
7. Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes
   Raquel Rabionet, James M Jaworski, Allison E. Ashley‐Koch, Eden R. Martin, James S. Sutcliffe, Jonathan L. Haines, G. Robert DeLong, Ruth K. Abramson, Harry H. Wright, Michael L. Cuccaro et al. · 2004 · Neuroscience Letters
8. Challenges and solutions for gene identification in the presence of familial locus heterogeneity
   Atteeq Ur Rehman, Regie Lyn P. Santos‐Cortez, Meghan C. Drummond, Mohsin Shahzad, Kwanghyuk Lee, Robert J. Morell, Muhammad Ansar, Abid Jan, Xin Wang, Abdul Aziz et al. · 2014 · European Journal of Human Genetics
9. Memory intensive AND/OR search for combinatorial optimization in graphical models
   Radu Marinescu, Rina Dechter · 2009 · Artificial Intelligence
10. A microsatellite linkage map of the blacklip abalone, Haliotis rubra
    Matthew Baranski, S. Loughnan, Christopher M. Austin · 2006 · Animal Genetics
11. Association analysis of polymorphic CGG repeat in 5′ UTR of the reelin and VLDLR genes with schizophrenia
    Akihisa Akahane, Hiroshi Kunugi, Hiroshi O. Tanaka, Shinichiro Nanko · 2002 · Schizophrenia Research
12. A family with X‐linked optic atrophy linked to the OPA2 locus Xp11.4‐Xp11.2
    Bradley J. Katz, Yu Zhao, Judith E. A. Warner · 2006 · American Journal of Medical Genetics Part A
13. Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communities
    Mi‐Hye Lee, Derek Gordon, Jürg Ott, Kangmo Lu, Leiv Ose, Tatu A. Miettinen, Helena Gylling, Anton F. H. Stalenhoef, Arti Pandya, Hideki Hidaka et al. · 2001 · European Journal of Human Genetics
14. Statistical Approaches to Gene Mapping
    Jürg Ott, Josephine J. Hoh · 2000 · The American Journal of Human Genetics
15. Description of the international consortium for prostate cancer genetics, and failure to replicate linkage of hereditary prostate cancer to 20q13
    Daniel J. Schaid, Bao Chang · 2004 · The Prostate
16. Defining the autism minimum candidate gene region on chromosome 7
    Holli B. Hutcheson, Yvonne M. Bradford, Susan E. Folstein, Marybeth Gardiner, Susan L. Santangelo, James S. Sutcliffe, Jonathan L. Haines · 2002 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
17. Linear trend tests for case–control genetic association that incorporate random phenotype and genotype misclassification error
    Derek Gordon, Chad A. Haynes, Yaning Yang, Patricia L. Kramer, Stephen J. Finch · 2007 · Genetic Epidemiology
18. Evaluation of a variant in the transcription factor 7‐like 2 (TCF7L2) gene and prostate cancer risk in a population‐based study
    Ilir Agalliu, Miia Suuriniemi, Ludmila Prokunina‐Olsson · 2008 · The Prostate
19. Mixed deterministic and probabilistic networks
    Robert Mateescu, Rina Dechter · 2008 · Annals of Mathematics and Artificial Intelligence
20. Brain white matter integrity and cortisol in older men: the Lothian Birth Cohort 1936
    Simon R. Cox, Mark E. Bastin, Karen J. Ferguson, Susana Muñoz Maniega, Sarah E. MacPherson, Ian J. Deary, Joanna Marguerite Wardlaw, Alasdair M. J. MacLullich · 2014 · Neurobiology of Aging
21. The Genetics of Polycystic Ovary Syndrome
    Brad Eilerman, Marzieh Salehi, Yaron Tomer · 2009 · Springer eBooks
22. Construction of high-resolution recombination maps in Asian seabass
    Le Wang, Bin Bai, Peng Liu, Shu Qing Huang, Zi Yi Wan, Elaine Chua, Baoqing Ye, Gen Hua Yue · 2017 · BMC Genomics
23. Association of a variation in the promoter region of the brain-derived neurotrophic factor gene with familial Parkinson's disease
    Abbas Parsian, Rashmi R. Sinha, Brad Alan Racette, Jing Hua Zhao, Joel S. Perlmutter · 2004 · Parkinsonism & Related Disorders
24. Statistical significance for hierarchical clustering in genetic association and microarray expression studies
    Mark A. Levenstien, Yaning Yang, Jürg Ott · 2003 · BMC Bioinformatics
25. Biological Models of Behavior and the Life Course
    Michael J. Shanahan, Scott Michael Hofer, Lilly Shanahan · 2007 · Springer eBooks
26. LINKAGE AND ASSOCIATION STUDIES OFIL1BANDIL1RNGENE POLYMORPHISMS IN PREECLAMPSIA
    Augusta M.A. Lachmeijer, M. P. Nosti-Escanilla, Esther Bastiaans et al. · 2002 · Hypertension in Pregnancy
27. Examination of association to autism of common genetic variationin genes related to dopamine
    Bernard M. Anderson, Nathalie C. Schnetz‐Boutaud, J. Bartlett, H.H. Wright, Ruth K. Abramson, Michael L. Cuccaro, John R. Gilbert, Margaret Ann Pericak‐Vance, Jonathan L. Haines · 2008 · Autism Research
28. A bibliography and comments on the use of statistical models in epidemiology in the 1980s
    Mitchell H. Gail · 1991 · Statistics in Medicine
29. Of replications and refutations: The status of Alzheimer’s disease genetic research
    Lars Bertram, Rudolph E. Tanzi · 2001 · Current Neurology and Neuroscience Reports
30. Characteristics of genetic markers and maps for cost‐effective genome screens using diallelic markers
    Katrina A.B. Goddard, Ellen M. Wijsman · 2002 · Genetic Epidemiology
31. Genome Scan of a Nonword Repetition Phenotype in Families with Dyslexia: Evidence for Multiple Loci
    Zoran Brkanac, Nicola H. Chapman, Robert P. Igo, Mark M. Matsushita, Kathleen H. Nielsen, Virginia Wise Berninger, Ellen M. Wijsman, Wendy H. Raskind · 2008 · Behavior Genetics
32. Possible association between the gamma-aminobutyric acid type B receptor 1 (GABBR1) gene and schizophrenia
    Gwyneth C. Zai, Nicole A. King, Gregory W.H. Wong, Cathy L. Barr, James L. Kennedy · 2005 · European Neuropsychopharmacology
33. Mutation screening and association of human retinoid X receptor γ variation with lipid levels in familial type 2 diabetes
    Hua Wang, Winston S. Chu, Christopher Hemphill, Sandra J. Hasstedt, Steven C. Elbein · 2002 · Molecular Genetics and Metabolism
34. Introduction and overview
    Robert C. Elston · 2000 · Statistical Methods in Medical Research
35. Does white matter structure or hippocampal volume mediate associations between cortisol and cognitive ageing?
    Simon R. Cox, Sarah E. MacPherson, Karen J. Ferguson, Natalie A. Royle, Susana Muñoz Maniega, María del C. Valdés Hernández, Mark E. Bastin, Alasdair M. J. MacLullich, Joanna Marguerite Wardlaw, Ian J. Deary · 2015 · Psychoneuroendocrinology
36. Linkage of a bipolar disorder susceptibility locus to human chromosome 13q32 in a new pedigree series
    Sarah H. Shaw, Zofi Mroczkowski‐Parker, Tatyana Shekhtman, Madeline Alexander, Ronald A. Remick, Adele Dessa Sadovnick, Susan L. McElroy, P E Keck, John R. Kelsoe · 2003 · Molecular Psychiatry
37. Post-genome respiratory epidemiology: a multidisciplinary challenge
    F. Kauffmann, the Post Genome Respiratory Epidemiology group · 2004 · European Respiratory Journal
38. Linkage analysis of ordinal traits for pedigree data
    Rui Feng, James Frederick Leckman, Heping Zhang D · 2004 · Proceedings of the National Academy of Sciences
39. Sequence variation in the transforming growth factor-β1 (TGFB1) gene and multiple sclerosis susceptibility
    A. J. Green, Lisa F. Barcellos, Jacqueline B. Rimmler et al. · 2001 · Journal of Neuroimmunology
40. Genetic Linkage Studies in Alopecia Areata
    Amalia Martı́nez-Mir, Abraham Zlotogorski, Jürg Ott · 2003 · Journal of Investigative Dermatology Symposium Proceedings
41. Regression Models for Linkage Heterogeneity Applied to Familial Prostate Cancer
    Daniel J. Schaid, Shannon K. McDonnell, Stephen N. Thibodeau · 2001 · The American Journal of Human Genetics
42. Novel integrative genomics strategies to identify genes for complex traits
    Eric E. Schadt · 2006 · Animal Genetics
43. Allelic association study between phospholipase A2 genes and bipolar affective disorder
    Ivanor Meira‐Lima, D. Jardim, Ricardo Magrani Junqueira · 2003 · Bipolar Disorders
44. Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies
    Anna González‐Neira, Juan Manuel Rosa-Rosa, Ana Osório et al. · 2007 · BMC Genomics
45. A Robust Multipoint Linkage Statistic (tlod) for Mapping Complex Trait Loci
    Victor Abkevich, Nicola J. Camp, Alexander Gutin · 2001 · Genetic Epidemiology
46. Polymorphism screening and haplotype analysis of the tryptophan hydroxylase gene (TPH1)and association with bipolar affective disorder in Taiwan
    Te-Jen Lai, Chia-Yen Wu, Hsu-Wen Tsai, Yi-Mei Joy Lin, H. Sunny Sun · 2005 · BMC Medical Genetics
47. Genetic study of the myelin oligodendrocyte glycoprotein (MOG) gene in schizophrenia
    Gwyneth C. Zai, Nicole A. King, K. Wigg, Jillian M. Couto, Gregory W.H. Wong, William G. Honer, Cathy L. Barr, James L. Kennedy · 2004 · Genes Brain & Behavior
48. Spectrum of Nonrandom Associations Between Microsatellite Loci on Human Chromosome 11p15
    Carlos Zapata, Santiago Rodrı́guez, Guillermo Visedo, Felipe Sacristán · 2001 · Genetics
49. Effect of heterogeneity and assumed mode of inheritance on lod scores
    Martina Durner, David A. Greenberg · 1992 · American Journal of Medical Genetics
50. Linkage Mapping in Aquaculture Species
    Roy G. Danzmann, Karim Gharbi · 2007
51. Community detection in directed acyclic graphs
    Leo Speidel, Taro Takaguchi, Naoki Masuda · 2015 · The European Physical Journal B
52. Association study between clinical response to rizatriptan and some candidate genes
    Carlo Asuni, A. Cherchi, Donatella Congiu · 2007 · The Journal of Headache and Pain
53. Chromosome 13q13–q14 locus overlaps mood and psychotic disorders: the relevance for redefining phenotype
    Michel Maziade, Yvon C Chagnon, Marc‐André Roy · 2009 · European Journal of Human Genetics
54. Are scurs in heterozygous polled (Pp) cattle a complex quantitative trait?
    Lilian Johanna Gehrke, Aurélien Capitan, Carsten Scheper et al. · 2020 · Genetics Selection Evolution
55. Allele-sharing among affected relatives: non-parametric methods for identifying genes
    Mei‐Chiung Shih, Alice S. Whittemore · 2001 · Statistical Methods in Medical Research
56. Evaluation of SRD5A2 sequence variants in susceptibility to hereditary and sporadic prostate cancer
    Bao‐Li Chang, S. Lilly Zheng, Sarah D. Isaacs · 2003 · The Prostate
57. The Interface of Genetics and Public Health: Research and Educational Challenges
    Melissa A. Austin, Patricia A. Peyser, Muin J. Khoury · 2000 · Annual Review of Public Health
58. Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE
    Johannes Dietter, Manuel Mattheisen, Robert Fürst, Franz Rüschendorf, Thomas F. Wienker, Konstantin Strauch · 2006 · Bioinformatics
59. Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
    Mine S. Cicek, Julie M. Cunningham, Brooke L. Fridley et al. · 2012 · PLoS ONE
60. Finding genes underlying human disease
    Catherine M. Stein, RC Elston · 2009 · Clinical Genetics
61. Linkage to 18qter differentiates two clinically overlapping syndromes: congenital cataracts-facial dysmorphism-neuropathy (CCFDN) syndrome and Marinesco-Sjögren syndrome
    Clotilde Lagier‐Tourenne, D Chaigne, J Gong, J Flori, M Mohr, D Ruh, D Christmann, J Flament, Jean‐Louis Mandel, Michel Koenig et al. · 2002 · Journal of Medical Genetics
62. Genetic diversity and population structure analysis of eight local chicken breeds of Southern Xinjiang
    W. Azimu, B. Manatbay, Yukun Li · 2018 · British Poultry Science
63. Confronting complexity in late‐onset Alzheimer disease: application of two‐stage analysis approach addressing heterogeneity and epistasis
    T. Thornton-Wells, J. H. Moore, E. Martin, M. Pericak-Vance, J. Haines · 2008 · Genetic Epidemiology
64. Family‐based association analysis of S100A8 genetic polymorphisms with aggressive periodontitis
    X. Y. Ren, Li Xu, Huanxin Meng, Huaxiang Zhao, Ruifang Lu, Z. B. Chen, Xiaodong Feng, Dongquan Shi, L. Zhang, Yu Tian · 2009 · Journal of Periodontal Research
65. Estimating genome-wide IBD sharing from SNP data via an efficient hidden Markov model of LD with application to gene mapping
    Sivan Bercovici, Christopher Meek, Ydo Wexler, Dan Geiger · 2010 · Bioinformatics
66. Design and analysis in genetic studies of human ageing and longevity
    Qihua Tan, Torben Arvid Kruse, Kaare Christensen · 2005 · Ageing Research Reviews
67. Genetics and clinical features of 15 Asian families with steroid-resistant nephrotic syndrome
    Akiko Kitamura, Hiroyasu Tsukaguchi, Kazumoto Iijima et al. · 2006 · Nephrology Dialysis Transplantation
68. Evaluation of apolipoprotein A-II as a positional candidate gene for familial Type II diabetes, altered lipid concentrations, and insulin resistance
    Steven C. Elbein, Weiwei Chu, Q. Ren, H. Wang, C. Hemphill, Sandra J. Hasstedt · 2002 · Diabetologia
69. Advancing drug discovery using the power of the human genome
    Karl Heilbron, Sahar V. Mozaffari, Vladimir Vacic, Peng Yue, Wei Wang, Jingchunzi Shi, Adrian M. Jubb, Steven J. Pitts, Xin Wang · 2021 · The Journal of Pathology
70. Toward the Human Genotope
    Peter Huggins, Lior S. Pachter, Bernd Sturmfels · 2007 · Bulletin of Mathematical Biology
71. Hot Regions of Noninterfering Crossovers Coexist with a Nonuniformly Interfering Pathway inArabidopsis thaliana
    Sayantani Basu-Roy, Franck Gauthier, Laurène Giraut · 2013 · Genetics
72. Exclusion mapping of the genetic predisposition for cervical artery dissections by linkage analysis
    Caspar Grond‐Ginsbach, Bernhard Klima, Ralf Weber · 2002 · Annals of Neurology
73. Genetic polymorphisms of the HCR gene and a genomic segment in close proximity to HLA-C are associated with patients with psoriasis in Taiwan
    Yun-Te Chang, Y.M. Shiao, Pei-Ju Chin et al. · 2004 · British Journal of Dermatology
74. Phenotypic definitions of psychotic illness for molecular genetic research
    ANNE E. FARMER, Julie H. Williams, Irene Jones · 1994 · American Journal of Medical Genetics
75. Analyses of hla linkage in white families with multiple cases of seropositive rheumatoid arthritis
    Rodney C.P. Go, Graciela S. Alarcón, Ronald T. Acton · 1987 · Arthritis & Rheumatism
76. The Evolving Field of Genetic Epidemiology: From Familial Aggregation to Genomic Sequencing
    Priya Duggal, Christine Ladd‐Acosta, Debashree Ray, Terri H. Beaty · 2019 · American Journal of Epidemiology
77. Genotype × Adiposity Interaction Linkage Analyses Reveal a Locus on Chromosome 1 for Lipoprotein-Associated Phospholipase A2, a Marker of Inflammation and Oxidative Stress
    Vincent P. Diego, David L. Rainwater, Xing-Li Wang, Shelley A. Cole, Joanne E. Curran, Matthew P. Johnson, Jeremy B. M. Jowett, Thomas D. Dyer, Jeff T. Williams, Eric Keith Moses et al. · 2006 · The American Journal of Human Genetics
78. XIBD: software for inferring pairwise identity by descent on the X chromosome
    Lyndal Henden, David Wakeham, Melanie Bahlo · 2016 · Bioinformatics
79. QTL Mapping in Intercross and Backcross Populations
    Fei Zou · 2009 · Methods in molecular biology
80. Copy-number-variation and copy-number-alteration region detection by cumulative plots
    Wentian Li, Annette Lee, Peter K. Gregersen · 2009 · BMC Bioinformatics
81. The complexity of checking consistency of pedigree information and related problems
    Luca Aceto, Jens A. Hansen, Anna Ingólfsdóttir · 2004 · Journal of Computer Science and Technology
82. A kindred with Parkinson’s disease not showing genetic linkage to established loci
    Katrina A. Gwinn, Richard Crook, S. J. Lincoln, Charles H. Adler, John N. Caviness, John Hardy, Matthew James Farrer · 2000 · Neurology
83. Genetics of Systemic Lupus Erythematosus: How Far Have We Come?
    Andrea L. Sestak, Swapan K. Nath, John B. Harley · 2005 · Rheumatic Disease Clinics of North America
84. Evaluation of microhaplotype panels for complex kinship analysis using massively parallel sequencing
    Jiaming Xue, Mengyu Tan, Ranran Zhang et al. · 2023 · Forensic Science International Genetics
85. Association between interleukin‐1 receptor antagonist gene and asthma‐related traits in a German adult population
    Cristian Pattaro, Joachim Heinrich, M. Werner · 2006 · Allergy
86. Molecular screening of the human glutamine–fructose-6-phosphate amidotransferase 1 (GFPT1) gene and association studies with diabetes and diabetic nephropathy
    Steven C. Elbein, Hailing Zheng, Yiwen Jia · 2004 · Molecular Genetics and Metabolism
87. Testing for Linkage and Association Across the Dihydrolipoyl Dehydrogenase Gene Region with Alzheimer’s Disease in Three Sample Populations
    Abraham M. Brown, Derek Gordon, Hsinhwa Lee, Fabienne Wavrant‐De Vrièze, Elena Cellini, Silvia Bagnoli, Benedetta Nacmias, Sandro Sorbi, John Hardy, John P. Blass · 2007 · Neurochemical Research
88. Association of the Exon 3 Deleted/Full-LengthGHRPolymorphism with Recombinant Growth Hormone Dose in Growth Hormone-Deficient Adults
    Silke Meyer, Stephan Schaefer, Lisette Stolk et al. · 2009 · Pharmacogenomics
89. Analysis of genetic diversity and phylogenetic relationships among red jungle fowls and Chinese domestic fowls
    Wenbin Bao, Guohong Chen, Bichun Li, Xinsheng Wu, Jingting Shu, Shenglong Wu, Qi Xu, Steffen Weigend · 2008 · Science in China Series C Life Sciences
90. Genome-wide linkage scan for prostate cancer susceptibility genes in men with aggressive disease: significant evidence for linkage at chromosome 15q12
    Ethan M. Lange, Lindsey A. Ho, Jennifer Beebe‐Dimmer · 2006 · Human Genetics
91. Linkage of autosomal dominant common variable immunodeficiency to chromosome 5p and evidence for locus heterogeneity
    David Braig, A.A. Schäffer, Erik Oliver Glocker · 2003 · Human Genetics
92. Spinal schistosomiasis
    Charles L. Gellido, S Onesti, Josefina F. Llena, M Suarez · 2000 · Neurology
93. Linkage analysis in heterogeneous and complex traits
    Jürg Ott, Ajita Bhat · 1999 · European Child & Adolescent Psychiatry
94. Epistasis Between Type 2 Diabetes Susceptibility Loci on Chromosomes 1q21‐25 and 10q23‐26 in Northern Europeans
    Steven Wiltshire, Jordana T. Bell, Christopher J. Groves, Christian Dina C, Andrew Tym Hattersley, Timothy M. Frayling, Mark Walker, G. A. Hitman, Martine Vaxillaire, Martin Farrall et al. · 2006 · Annals of Human Genetics
95. X chromosomal recombination—A family study analyzing 26 X ‐ STR L oci in C hinese H an three‐generation pedigrees
    Qiu‐Ling Liu, Ze‐Dong Li, Chengtao Li · 2013 · Electrophoresis
96. Genome-wide linkage scan for spontaneous DZ twinning
    Catherine A Derom, Damini Jawaheer, Wei V. Chen · 2005 · European Journal of Human Genetics
97. A quantitative analysis of Educational Data through the Comparison between Hierarchical and Not-Hierarchical Clustering
    Onofrio Rosario Battaglia, Benedetto Di Paola, Claudio Fazio · 2017 · Eurasia Journal of Mathematics Science and Technology Education
98. Nontuberculous mycobacterial cervicofacial lymphadenitis in children from the multicenter, randomized, controlled trial in The Netherlands: Relevance of polymorphisms in candidate host immunity genes
    Margje H. Haverkamp, Jerome A. H. Lindeboom, Adriëtte W. de Visser, Dennis Kremer, Taco Willem Kuijpers, Esther van de Vosse, Jaap T. van Dissel · 2010 · International Journal of Pediatric Otorhinolaryngology
99. Determinants of variation in serum paraoxonase enzyme activity in baboons
    David L. Rainwater, Michael C. Mahaney, Xing Li Wang, Jeffrey Rogers, Laura A. Cox, John L. VandeBerg · 2005 · Journal of Lipid Research
100. Optimized Group Sequential Study Designs for Tests of Genetic Linkage and Association in Complex Diseases
     Inke Regina König, H. -J. Schäfer, Hans‐Helge Müller · 2001 · The American Journal of Human Genetics