Analysis of Human Genetic Linkage

Cited by (755)

Items 401–500 of 755

1. Assessing accuracy in linkage analysis by means of confidence regions
   Ola Hössjer · 2003 · Genetic Epidemiology
2. How useful is the fine-scale mapping of complex trait linkage peaks? Evaluating the impact of additional microsatellite genotyping on the posterior probability of linkage
   Steven Wiltshire, Andrew P. Morris, Mark I. McCarthy, Lon R. Cardon · 2004 · Genetic Epidemiology
3. Genetical genomics of Th1 and Th2 immune response in a baboon model of atherosclerosis risk factors
   Amanda Vinson, Joanne E. Curran, Mathew P. Johnson, Tom Dyer, Eric Keith Moses, John Blangero, Laura A. Cox, J. Rogers, Lorena M. Havill, John L. VandeBerg et al. · 2011 · Atherosclerosis
4. Multiple Interval Mapping for Quantitative Trait Loci via EM Algorithm in the Presence of Crossover Interference
   Ying Zhou · 2010 · Communication in Statistics- Theory and Methods
5. Flies, Genes, and Brains: Oskar Vogt, Nikolai Timoféeff-Ressovsky, and the Origin of the Concepts of Penetrance and Expressivity
   Manfred D. Laubichler, Sahotra Sarkar · 2002 · Philosophy and medicine
6. Re-Sequencing Data for Refining Candidate Genes and Polymorphisms in QTL Regions Affecting Adiposity in Chicken
   Pierre‐François Roux, Morgane Boutin, Colette Désert, Anis Djari, Diane Esquerré, Christophe Klopp, Sandrine Lagarrigue, Olivier Demeure · 2014 · PLoS ONE
7. Genetic diversity and the structure of linkage disequilibrium in the methylenetetrahydrofolate reductase locus
   Ekaterina A. Trifonova, М. Г. Спиридонова, В. А. Степанов · 2008 · Russian Journal of Genetics
8. Pedigree-Defined Haplotypes and Their Applications to Genetic Studies
   Chester A. Alper, Charles E. Larsen · 2017 · Methods in molecular biology
9. Evaluation of sequence variants in the pre-B cell leukemia transcription factor 1 gene: A positional and functional candidate for type 2 diabetes and impaired insulin secretion
   Hua Wang, Winston S. Chu, Xiaoqin Wang, Zhengxian Zhang, Steven C. Elbein · 2005 · Molecular Genetics and Metabolism
10. A unified theory of autism revisited: linkage evidence points to chromosome X using a high‐risk subset of AGRE families
    Kristina Allen‐Brady, Dale S. Cannon, Reid J. Robison, William M. McMahon, Hilary H Coon · 2010 · Autism Research
11. Individual-Specific Liability Groups in Genetic Linkage, with Applications to Kindreds with Li-Fraumeni Syndrome
    Sanjay S. Shete, Christopher I. Amos, Shih-Jen Hwang · 2002 · The American Journal of Human Genetics
12. Building chromosome-wide LD maps
    María M. Abad‐Grau, Rosana Montes, Paola Sebastiani · 2006 · Bioinformatics
13. Neurogenetics: single gene disorders
    S-M Pulst · 2003 · Journal of Neurology Neurosurgery & Psychiatry
14. Landscaping Crossover Interference Across a Genome
    Lidan Sun, Jing Wang, Mengmeng Sang · 2017 · Trends in Plant Science
15. The Association of Aquaporin-1 Gene with Marathon Running Performance Level: a Confirmatory Study Conducted in Male Hispanic Marathon Runners
    Miguel A. Rivera, Thomas Davin Fahey, Juan Ricardo Lopez-Taylor, Juan López-Quiles Martínez · 2020 · Sports Medicine - Open
16. Allele frequencies of 14 STR loci in the population of Malta
    M. Cassar, Cécile Farrugia, Christopher Vidal · 2007 · Legal Medicine
17. A study comparing precision of the maximum multipoint heterogeneity LOD statistic to three model‐free multipoint linkage methods
    Stephen J. Finch, Chien‐Hsiun Chen, Derek Gordon · 2001 · Genetic Epidemiology
18. No association between common variations in the neuronal nicotinic acetylcholine receptor alpha2 subunit gene (CHRNA2) and bipolar I disorder
    Falk W. Lohoff, Thomas N. Ferraro, Leilah McNabb · 2005 · Psychiatry Research
19. A novel genetic modifier of p53, mop1, results in embryonic lethality
    Susan C. Evans, Min Liang, Christopher Amos, Xiangjun Gu, Guillermina Lozano · 2004 · Mammalian Genome
20. Asthma, Allergy, and Airway Hyperresponsiveness Are Not Linked to the β2-Adrenoceptor Gene
    Charles W. Emala, Christopher K. McQuitty, Scott M. Eleff · 2002 · CHEST Journal
21. Family-based association tests for quantitative traits using pooled DNA
    Joel S. Bader, Pak Chung Sham · 2002 · European Journal of Human Genetics
22. The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data
    Elizabeth Holliday, Bryan J. Mowry, David Charles Chant, Dale R. Nyholt · 2005 · Human Genetics
23. Multivariate genetic analysis of an oligogenic disease
    Steven O. Moldin, Paul Van Eerdewegh · 1995 · Genetic Epidemiology
24. Linkage analysis in juvenile neuronal ceroid lipofuscinosis
    Jonathan L. Haines, Wei‐Lang Yan, Rose‐Mary Boustany · 1992 · American Journal of Medical Genetics
25. Two Approaches for Consolidating Results from Genome Scans of Complex Traits: Selection Methods and Scan Statistics
    Derek Gordon, Josephine J. Hoh, Stephen J. Finch · 2001 · Genetic Epidemiology
26. Recombination analysis of autosomal short tandem repeats in C hinese H an families
    Qiuling Liu, Hong Luo, Hu Zhao, Xiaoling Huang, Jianding Cheng, De-Jian Lü · 2013 · Electrophoresis
27. Allelic structure and distribution of 103 STR loci in a Southern Tunisian population
    Abdellatif Maalej, Ahmed Rebaï, Adnene Ayadi, Jomaa Jouida, H. Makni, Hammadi Ayadi · 2004 · Journal of Genetics
28. Target-Site Resistances to ALS and PPO Inhibitors Are Linked in Waterhemp (Amaranthus tuberculatus)
    Patrick J. Tranel, Chenxi Wu, Ahmed Sadeque · 2016 · Weed Science
29. A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families
    Lisbeth Venø Kruse, Mette Nyegaard, Ulla Christensen et al. · 2012 · European Journal of Human Genetics
30. Analysis of coding variants in the betacellulin gene in type 2 diabetes and insulin secretion in African American subjects
    Steven C. Elbein, Xiaoqin Wang, Mohammad Azharul Karim, Winston S. Chu, Kristi D. Silver · 2006 · BMC Medical Genetics
31. A genome-wide search replicates evidence of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE) unlinked to the ACE gene
    Colin A. McKenzie, Xiaofeng Zhu, Terrence E. Forrester, Amy Luke, Adebowale Adeyemo, Nourdine Bouzekri, Richard Cooper · 2008 · BMC Medical Genomics
32. Linkage and Association Analysis Identifies TRAF1 Influencing Common Carotid Intima–Media Thickness
    Nicole Heßler, Marie Henrike Geisel, Stefan Coassin, Raimund Erbel, Stefanie Heilmann‐Heimbach, Frauke Hennig, Barbara H. Hoffmann, Karl‐Heinz Jöckel, Susanne Moebus, Susanna Moskau‐Hartmann et al. · 2016 · Stroke
33. Designing Optimally Multiplexed SNP Genotyping Assays
    Yonatan Aumann, Efrat Manisterski, Zohar Yakhini · 2003 · Lecture notes in computer science
34. Joint linkage and segregation analysis under multiallelic trait inheritance: simplifying interpretations for complex traits
    Elisabeth A. Rosenthal, Ellen M. Wijsman · 2010 · Genetic Epidemiology
35. Bayesian estimates of linkage disequilibrium
    Paola Sebastiani B, María M. Abad‐Grau · 2007 · BMC Genetics
36. Genetics, Genomics, Proteomics, and Bioinformatics
    Peter Andreas Kopp · 2005 · Clinical Pediatric Endocrinology
37. Checking Consistency of Pedigree Information is NP-complete (Preliminary Report)
    Luca Aceto, Jens Alsted Hansen, Anna Ingólfsdóttir · 2002 · BRICS Report Series
38. Genetic Discoveries in Atrial Fibrillation and Implications for Clinical Practice
    Saagar Mahida, Leeds General Infirmary, Great George Street, Leeds, LS1 3EX, UK. E: saagar7m7@yahoo.co.uk · 2014 · Arrhythmia & Electrophysiology Review
39. Identification of QTL and loci for egg production traits to tropical climate conditions in chickens
    Ching-Yi Lien, Michèle Tixier‐Boichard, Shih-Wen Wu · 2020 · Livestock Science
40. New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involving TWIST1 regulatory elements
    Vanessa Luiza Romanelli Tavares, Sofia Lígia Guimarães Ramos, Yan Zhou, Cibele Masotti, Suzana Ezquina, Danielle de Paula Moreira, Henk P.J. Buermans, Renato S Freitas, Johan T. den Dunnen, Stephen R.F. Twigg et al. · 2021 · Journal of Medical Genetics
41. Substantial Linkage Disequilibrium Across the Dihydrolipoyl Succinyltransferase Gene Region Without Alzheimer's Disease Association
    Abraham M. Brown, Derek Gordon, Hsinhwa Lee, Michael A. Caudy, Vahram H. Haroutunian, John P. Blass · 2004 · Neurochemical Research
42. Sample Reproducibility of Genetic Association Using Different Multimarker TDTs in Genome-Wide Association Studies: Characterization and a New Approach
    María M. Abad‐Grau, Nuria Medina-Medina, Rosana Montes, Fuencisla Matesanz, Vineet Bafna · 2012 · PLoS ONE
43. Using Linkage Analysis to Detect Gene-Gene Interactions. 2. Improved Reliability and Extension to More-Complex Models
    Susan E. Hodge, Valerie R. Hager, David A. Greenberg · 2016 · PLoS ONE
44. Genetic Linkage Studies
    Ezra Susser, Sharon Schwartz, Alfredo Morabia · 2006
45. Linkage, recombination, and mutation rate analyses of 19 X-chromosomal STR loci in Chinese Southern Han pedigrees
    Xingyi Yang, Yutian Chen, Xiangpei Zeng et al. · 2019 · International Journal of Legal Medicine
46. A Likelihood Ratio Test for Genome‐Wide Association under Genetic Heterogeneity
    Qian Meng, Yongzhao Shao · 2013 · Annals of Human Genetics
47. Localization of an acromesomelic dysplasia on chromosome 9 by homozygosity mapping
    Peter Ianakiev, M W Kilpatrick, MJ Daly · 2000 · Clinical Genetics
48. Modeling the effect of inbreeding among founders in linkage analysis
    Ola Hössjer · 2006 · Theoretical Population Biology
49. Affective disorder not linked to HLA
    R. Arlen Price · 1989 · Genetic Epidemiology
50. Linkage Analysis, Model‐Based
    Joseph Douglas Terwilliger · 2005 · Encyclopedia of Biostatistics
51. Reducing sample sizes in genome scans: Group sequential study designs with futility stops
    Inke Regina König, H. -J. Schäfer, Andreas Ziegler · 2003 · Genetic Epidemiology
52. Genetic Analysis: Moving between Linkage and Association
    Albert V. Smith · 2012 · Cold Spring Harbor Protocols
53. The Genetics of Familial and Non-Familial Hyperthyroid Graves’ Disease
    Y. Tomer, T. Davies · 2000 · Endocrine updates
54. Likelihood Approach for Detecting Imprinting and In Utero Maternal Effects Using General Pedigrees from Prospective Family‐Based Association Studies
    Jingyuan Yang, Shili Lin · 2011 · Biometrics
55. No Association between SNP rs498055 on Chromosome 10 and Late‐Onset Alzheimer Disease in Multiple Datasets
    Xueying Sharon Liang, Nathalie C. Schnetz‐Boutaud, Jackie Bartlett · 2007 · Annals of Human Genetics
56. Refined mapping of the autosomal recessive non‐syndromic deafness locus DFNB13 using eight novel microsatellite markers
    Saber Masmoudi, Ilhem Charfedine, IB Rebeh · 2004 · Clinical Genetics
57. Analysis of Genetic Linkage Data for Mendelian Traits
    Nicole Dueker, Margaret Ann Pericak‐Vance · 2014 · Current Protocols in Human Genetics
58. The power to detect genetic linkage for quantitative traits in the Utah CEPH pedigrees
    Alka Malhotra, Kevin Cromer, Mark Leppert · 2005 · Journal of Human Genetics
59. A simple method for detection of imprinting effects based on case–parents trios
    J-Y Zhou, Y-Q Hu, Wing K. Fung · 2006 · Heredity
60. A reanalysis of 409 European‐Ancestry and African American schizophrenia pedigrees reveals significant linkage to 8p23.3 with evidence of locus heterogeneity
    Elizabeth Holliday, Bryan J. Mowry, D. Nyholt · 2008 · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
61. Interest of X chromosome (Argus X-12 kit) in complex kinship analysis
    Laura Cainé, Raquel Carvalho, Sérgio Costa · 2011 · Forensic science international. Genetics supplement series
62. Refined assignment of the infantile neuronal ceroid‐lipofuscinosis (INCL) locus at 1p32 and the current status of prenatal and carrier diagnostics
    Elina Hellsten, Jouni Vesa, Irma E. Järvelä · 1993 · Journal of Inherited Metabolic Disease
63. Designing an optimum genetic association study using dense SNP markers and family-based sample
    C. Charles Gu · 2003 · Frontiers in bioscience
64. Integrating genotypic data with transcriptomic and proteomic data
    Denis C. Shields, Aisling M O’Halloran · 2002 · Comparative and Functional Genomics
65. Genetic association tests for family data with missing parental genotypes: A comparison
    Alice S. Whittemore, Jerry Halpern · 2003 · Genetic Epidemiology
66. How do stochastic processes and genetic threshold effects explain incomplete penetrance and inform causal disease mechanisms?
    Jenkins, Dagan · 2024 · Philosophical Transactions of the Royal Society B: Biological Sciences
67. Who named it? www.whonamedit.com
    Andrew J. Larner · 2003 · Journal of Neurology Neurosurgery & Psychiatry
68. Dopamine Genes and Sensory Sensitivity as a Temperamental Trait
    Wojciech Łukasz Dragan, Włodzimierz Oniszczenko, Piotr M. Czerski · 2012 · Journal of Individual Differences
69. The ADH gene cluster SNP rs1789891 and temperamental dimensions in patients with alcohol dependence and affective disorders
    Włodzimierz Oniszczenko, JANUSZ K. RYBAKOWSKI, Wojciech Łukasz Dragan, Anna Grzywacz, Jerzy Samochowiec · 2015 · Scandinavian Journal of Psychology
70. Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families
    Joan E. Bailey‐Wilson, Erica J. Childs, Cheryl D. Cropp et al. · 2012 · BMC Medical Genetics
71. Meta-analysis of quantitative pleiotropic traits for next-generation sequencing with multivariate functional linear models
    Chi‐Yang Chiu, Jeesun Jung, Wei Chen, Daniel E. Weeks, Haobo Ren, Michael Boehnke, Christopher Ian Amos, Aiyi Liu, James L. Mills, Mei‐Ling Ting Lee et al. · 2016 · European Journal of Human Genetics
72. A Novel Locus for X-linked Retinitis Pigmentosa
    Zongzhong Tong, Zhenglin Yang, Jay J. Meyer, Allen W McInnes, Xue Lai, Asif M. Azimi, Jenn Baird, Yu Zhao, Erik Pearson, Changguan Wang et al. · 2006 · Annals of the Academy of Medicine Singapore
73. A Marginal Likelihood Model for Family‐Based Data
    Shaw‐Hwa Lo, Xin Liu, Yongzhao Shao · 2003 · Annals of Human Genetics
74. Distribution of model‐based multipoint heterogeneity lod scores
    Chao Xing, Nathan J. Morris, Guan Xing · 2010 · Genetic Epidemiology
75. Improving estimates of genetic maps: a meta‐analysis‐based approach
    William C. L. Stewart · 2007 · Genetic Epidemiology
76. The Evaluation of DNA Evidence in Pedigrees Requiring Population Inference
    Fabio Corradi, Giampietro Lago, Federico Mattia Stefanini · 2003 · Journal of the Royal Statistical Society Series A (Statistics in Society)
77. Analysis of Genetic Linkage
    Rita M. Cantor · 2014 · Elsevier eBooks
78. Linkage and Association Studies
    Ingrid B. Borecki · 2006 · Encyclopedia of Life Sciences
79. Information and effective number of meioses in linkage analysis
    Ola Hössjer · 2004 · Journal of Mathematical Biology
80. Comparison of methods incorporating quantitative covariates into affected sib pair linkage analysis
    Hui‐Ju Tsai, Daniel E. Weeks · 2005 · Genetic Epidemiology
81. On modeling locus heterogeneity using mixture distributions.
    Shili Lin, Swati Biswas · 2004 · BMC Genetics
82. Survival Analysis: Lessons from Quantitative Genetics
    Lindon J. Eaves · 1987 · Springer eBooks
83. Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test
    María M. Abad‐Grau, Nuria Medina-Medina, Rosana Montes, José Javier Moreno-Ortega, Fuencisla Matesanz · 2010 · Human Genetics
84. Genetic variability determination in a long-term selected Rhode Island Red chicken strain using microsatellite markers
    Abdul Rahim, Sanjeev Kumar, Ramji Yadav · 2017 · Veterinarski arhiv
85. Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk
    Nandita Mukhopadhyay, Janelle Annette Noble, Manika Govil · 2018 · PLoS ONE
86. Heterogeneity in Statistical Genetics
    Derek Gordon, Stephen J. Finch, Wonkuk Kim · 2020 · Statistics for biology and health
87. Resolving the recombination pattern of 38 X-STRs from Chinese Han three-generation pedigrees
    Feng Song, Xiaowen Wei, Chengye Zhou · 2022 · Legal Medicine
88. INCREASING POWER BY USING HAPLOTYPE SIMILARITY IN A MULTIMARKER TRANSMISSION/DISEQUILIBRIUM TEST
    María M. Abad‐Grau, Nuria Medina-Medina, Serafı́n Moral · 2012 · Journal of Bioinformatics and Computational Biology
89. Group sequential testing of homogeneity in genetic linkage analysis
    Yin Cui, Yuejiao Fu, Abdulkadir A. Hussein · 2009 · Computational Statistics & Data Analysis
90. A comparison of different linkage statistics in small to moderate sized pedigrees with complex diseases
    Antònia Flaquer, Konstantin Strauch · 2012 · BMC Research Notes
91. The Identification of Colon Cancer Susceptibility Genes by Using Genome-Wide Scans
    Denise Daley · 2010 · Methods in molecular biology
92. Genetic Epidemiology of Complex Phenotypes
    Lynette Peddle, Proton Rahman · 2008 · Methods in molecular biology
93. The Rise and Fall and Rise of Linkage Analysis as a Technique for Finding and Characterizing Inherited Influences on Disease Expression
    Ettie M. Lipner, David A. Greenberg · 2018 · Methods in molecular biology
94. Linkage Analysis
    Jennifer H. Barrett, M. Dawn Teare · 2011 · Methods in molecular biology
95. Network-based quantitative trait linkage analysis of microbiome composition in inflammatory bowel disease families
    Arunabh Sharma, Olaf Junge, Silke Szymczak, Malte Christoph Rühlemann, Janna Enderle, Stefan Schreiber, Matthias Laudes, André Franke, Wolfgang Lieb, Michael Krawczak et al. · 2023 · Frontiers in Genetics
96. Genetic Linkage Analysis Algorithms and Their Implementation
    Anna Ingólfsdóttir, Daniel Fannar Gudbjartsson · 2005 · Lecture notes in computer science
97. Methods for Combining Multiple Genome-Wide Linkage Studies
    Trecia A. Kippola, Stephanie A. Santorico · 2009 · Methods in molecular biology
98. Maximum‐likelihood estimation in linkage heterogeneity models including additional information via the EM algorithm
    Jeanine J. Houwing‐Duistermaat, Lodewijk A. Sandkuijl, Arthur A B Bergen · 1995 · Genetic Epidemiology
99. Allele sharing and allelic association I: Sib pair tests with increased power
    Laura C. Lazzeroni · 2002 · Genetic Epidemiology
100. Unraveling the genetics of atherosclerosis: implications for diagnosis and treatment
     David Seo, Pascal J. Goldschmidt‐Clermont · 2006 · Expert Review of Molecular Diagnostics