Analysis of Human Genetic Linkage

Cited by (755)

Items 301–400 of 755

1. 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
2. Genome‐wide identity‐by‐descent sharing among CEPH siblings
   Alain Gagnon, Jan Beise, James W. Vaupel · 2005 · Genetic Epidemiology
3. EM-random forest and new measures of variable importance for multi-locus quantitative trait linkage analysis
   Sophia S. F. Lee, Lei Sun, Rafal Kustra · 2008 · Bioinformatics
4. A pleiotropic QTL on 2p influences serum Lp-PLA2 activity and LDL cholesterol concentration in a baboon model for the genetics of atherosclerosis risk factors
   Amanda Vinson, Michael C. Mahaney, Laura A. Cox · 2007 · Atherosclerosis
5. Annotating individual human genomes
   Ali Torkamani, Ashley A. Scott‐Van Zeeland, Eric J. Topol, Nicholas J. Schork · 2011 · Genomics
6. Convergence of Advances in Genomics, Team Science, and Repositories as Drivers of Progress in Psychiatric Genomics
   Thomas Lehner, Geetha Senthil, Anjene Musick Addington · 2014 · Biological Psychiatry
7. QTL affecting stress response to crowding in a rainbow trout broodstock population
   Caird E. Rexroad, Roger L. Vallejo, Sixin Liu · 2012 · BMC Genetics
8. Linkage and association of phospholipid transfer protein activity to LASS4
   Elisabeth A. Rosenthal, James Ronald, Joseph H. Rothstein, Ramakrishnan Rajagopalan, Jane Ranchalis, Gertrud Wolfbauer, John J. Albers, John D. Brunzell, Arno G. Motulsky, Mark J. Rieder et al. · 2011 · Journal of Lipid Research
9. Speeding up HMM algorithms for genetic linkage analysis via chain reductions of the state space
   Dan Geiger, Christopher Meek, Ydo Wexler · 2009 · Bioinformatics
10. Association of the dihydrolipoamide dehydrogenase gene with Alzheimer's disease in an Ashkenazi Jewish population
    Abraham M. Brown, Derek Gordon, Hsinhwa Lee, Michael A. Caudy, John Hardy, Vahram H. Haroutunian, John P. Blass · 2004 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
11. AFLP linkage map of sea urchin constructed using an interspecific cross between Strongylocentrotus nudus (♀) and S. intermedius (♂)
    Zunchun Zhou, Zhenmin Bao, Ying Dong · 2006 · Aquaculture
12. Molecular screening and association studies of retinoid-related orphan receptor γ (RORC): a positional and functional candidate for type 2 diabetes
    Hua Wang, Winston S. Chu, Swapan K. Das, Zhengxian Zheng, Sandra J. Hasstedt, Steven C. Elbein · 2003 · Molecular Genetics and Metabolism
13. Current perspectives on the genetic analysis of autism
    Hilary H Coon · 2006 · American Journal of Medical Genetics Part C Seminars in Medical Genetics
14. Detection of QTL for body weight and body fat content in mice using genetic markers
    G. A. Brockmann, D. Timtchenko, P. Das · 1996 · Journal of Animal Breeding and Genetics
15. Genetics of Interactive Behavior in Silver Foxes (Vulpes vulpes)
    Ronald M. Nelson, Svetlana V. Temnykh, Jennifer Lynn Johnson, Anastasiya V. Kharlamova, Anastasiya V. Vladimirova, Rimma G. Gulevich, Darya V. Shepeleva, I. N. Oskina, Gregory M. Acland, Lars Rönnegård et al. · 2016 · Behavior Genetics
16. Detection of QTL for traits related to adaptation to sub-optimal climatic conditions in chickens
    Ching-Yi Lien, Michèle Tixier‐Boichard, Shih-Wen Wu · 2017 · Genetics Selection Evolution
17. The Genetic Epidemiology of Growth and Development
    Bradford Towne, Ellen W. Demerath, Stefan A. Czerwinski · 2012 · Elsevier eBooks
18. Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus
    Xin Liang, Nathalie C. Schnetz‐Boutaud, Shannon J. Kenealy et al. · 2005 · Molecular Psychiatry
19. A_16_C haplotype in the FcεRIβ gene confers a higher risk for atopic asthma in the Indian population
    Shilpy Sharma, Rana Nagarkatti, Chandrika B‐Rao, Pramod V. Niphadkar, V K Vijayan, SK Sharma, Balaram Ghosh · 2004 · Clinical Genetics
20. A Confidence-Set Approach for Finding Tightly Linked Genomic Regions
    Shili Lin, James Allen Rogers, Jason C. Hsu · 2001 · The American Journal of Human Genetics
21. Identification of linked regions using high-density SNP genotype data in linkage analysis
    Guohui Lin, Zhanyong Wang, Lusheng Wang · 2007 · Bioinformatics
22. On finite mixture models
    Jiahua Chen · 2017 · Statistical Theory and Related Fields
23. The Phe‐124‐Cys and A‐161T Variants of the Human 5‐HT 1B Receptor Gene Are Not Major Determinants of the Clinical Response to Sumatriptan
    Suneet Mehrotra, Kaate R. J. Vanmolkot, Rune R. Frants · 2007 · Headache The Journal of Head and Face Pain
24. Population Isolates in South Tyrol and Their Value for Genetic Dissection of Complex Diseases
    Fabio Marroni, Irene Pichler, Alessandro De Grandi, Cláudia B. Volpato, Florian D. Vogl, Gerd K. Pinggera, Joan Wilson, Peter Paul Pramstaller · 2006 · Annals of Human Genetics
25. 10 Major strengths and weaknesses of the lod score method
    Jürg Ott · 2001 · Advances in genetics
26. QTL detection for coccidiosis (Eimeria tenella) resistance in a Fayoumi × Leghorn F2 cross, using a medium-density SNP panel
    Nicola Bacciu, Bertrand Bed’Hom, Olivier Filangi · 2014 · Genetics Selection Evolution
27. RC_Link: Genetic linkage analysis using Bayesian networks
    David L. Allen, Adnan Y. Darwiche · 2007 · International Journal of Approximate Reasoning
28. An AFLP linkage map for Douglas-fir based upon multiple full-sib families
    Nicholas K. Ukrainetz, Kermit Ritland, Shawn D. Mansfield · 2007 · Tree Genetics & Genomes
29. Examining the effect of linkage disequilibrium on multipoint linkage analysis
    Qiqing Huang, Sanjay S. Shete, Michael D. Swartz · 2005 · BMC Genetics
30. Psychogeriatric Research: A Conceptual Introduction to Aging and Geriatric Neuroscience
    Ramón Cacabelos · 2001 · Psychogeriatrics
31. Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defects
    Bruno Saint-Jore, Mathilde Varret, Christiane Dachet et al. · 2000 · European Journal of Human Genetics
32. Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses: ELAC2 and familial early‐onset prostate cancer
    Nicola J. Camp, Jeffrey J. Swensen, Benjamin Davies Horne · 2004 · Genetic Epidemiology
33. Exploring the genetic basis of diseases through a heterogeneous bibliometric network: A methodology and case study
    Mengjia Wu, Yi Zhang, Guangquan Zhang, Jie Lü · 2020 · Technological Forecasting and Social Change
34. Replication of linkage with bipolar disorder on chromosome 16p in the eastern Quebec population
    Chantal Mérette, Marc‐André Roy, Alexandre Bureau, Alain Fournier, Claudia Émond, Denis Cliche, Valérie Jomphe, Yvon C. Chagnon, Michel Maziade · 2007 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
35. Hypothesis Testing in a Mixture Case-Control Model
    Jing Qin, Kung‐Yee Liang · 2010 · Biometrics
36. Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease
    Xueying Sharon Liang, Eden R. Martin, Nathalie C. Schnetz‐Boutaud, Jackie Bartlett, Brent C. Anderson, Stephan L. Zuchner, Harry E. Gwirtsman, Don E. Schmechel, Regina M. Carney, John R. Gilbert et al. · 2007 · Human Mutation
37. The role of candidate genes in unraveling the genetics of autism
    Chris Stodgell, Jennifer L. Ingram, Susan L Hyman · 2000 · International review of research in mental retardation
38. Putative Susceptibility Locus on Chromosome 21q for Lumbar Disc Disease (LDD) in the Finnish Population
    Iita M. Virtanen, Noora Noponen, Sandra Barral · 2007 · Journal of Bone and Mineral Research
39. Linkage analysis of candidate endothelin pathway genes in nonsyndromic familial orofacial cleft
    Furio Pezzetti, Luca Scapoli, Marcella Martinelli · 2000 · Annals of Human Genetics
40. Linkage disequilibrium mapping of novel lung tumor susceptibility quantitative trait loci in mice
    Daolong Wang, William J. Lemon, Ming You · 2002 · Oncogene
41. A likelihood-based extended admixture model of oligogenic inheritance in ‘model-based’ and ‘model-free’ analysis
    Joseph Douglas Terwilliger · 2000 · European Journal of Human Genetics
42. Genotype-by-diet effects on co-variation in Lp-PLA2 activity and LDL-cholesterol concentration in baboons fed an atherogenic diet
    Amanda Vinson, Michael C. Mahaney, Vincent P. Diego, Laura A. Cox, Jeffrey Rogers, John L. VandeBerg, David L. Rainwater · 2008 · Journal of Lipid Research
43. Power and Effective Study Size in Heritability Studies
    Jesse D. Raffa, E. A. Thompson · 2016 · Statistics in Biosciences
44. MGST2 and WNT2 are candidate genes for comitant strabismus susceptibility in Japanese patients
    Jingjing Zhang, Toshihiko Matsuo · 2017 · PeerJ
45. Molecular genetics of autism
    Rita M. Cantor · 2009 · Current Psychiatry Reports
46. Investigation of polymorphisms in the CREM gene in panic disorder
    Steven P. Hamilton, Susan L. Slager, David Mayo · 2003 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
47. p75NTR gene and suicide attempts in young adults with a history of childhood‐onset mood disorder
    Stuart McGregor, J. Strauss, Natalie Bulgin, Vincenzo De Luca, Charles J. George, Mária Kovács, James L. Kennedy · 2007 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
48. Clinical and genetic investigation of isolated microspherophakia in a consanguineous Tunisian family
    Salim Ben Yahia, Farah Ouechtati, Béchir Jelliti · 2009 · Journal of Human Genetics
49. Examination of tetrahydrobiopterin pathway genes in autism
    Nathalie C. Schnetz‐Boutaud, Bernard M. Anderson, K. D. Brown, H. H. Wright, Ruth K. Abramson, Michael L. Cuccaro, John R. Gilbert, Margaret Ann Pericak‐Vance, Jonathan L. Haines · 2009 · Genes Brain & Behavior
50. Marker-assisted assessment of genotype by environment interaction: A case study of single nucleotide polymorphism-mortality association in broilers in two hygiene environments1
    N. Long, Daniel Gianola, Guilherme J. M. Rosa · 2008 · Journal of Animal Science
51. An Ancient, MHC-Linked, Nonclassical Class I Lineage in Cartilaginous Fish
    Tereza Almeida, Pedro José Esteves, Martin F. Flajnik · 2020 · The Journal of Immunology
52. Segregation and linkage analysis*
    Robert C. Elston · 1992 · Animal Genetics
53. Vitamin D Receptor Gene Polymorphisms Predict Acquired Resistance to Clodronate Treatment in Patients with Paget’s Disease of Bone
    Giuseppe Mossetti, Luigi Gennari, Domenico Rendina et al. · 2008 · Calcified Tissue International
54. Computing Power and Sample Size for Case-Control Association Studies with Copy Number Polymorphism: Application of Mixture-Based Likelihood Ratio Test
    Wonkuk Kim, Derek Gordon, Jonathan L. Sebat · 2008 · PLoS ONE
55. A Train of Thoughts on Gene Mapping
    Josephine Hoh, Jürg Ott · 2001 · Theoretical Population Biology
56. X chromosomal recombination study in three-generation families in Hungary
    Horolma Pamjav, Renáta Kugler, Andrea Zalán · 2011 · Forensic Science International Genetics
57. A score for Bayesian genome screening
    E. Warwick Daw, Ellen Marie Wijsman, E. A. Thompson · 2003 · Genetic Epidemiology
58. Assignment of chromosomal locations for unassigned SNPs/scaffolds based on pair-wise linkage disequilibrium estimates
    Mehar Singh Khatkar, Matthew Hobbs, Markus Neuditschko, Johann Sölkner, Frank W. Nicholas, Herman W. Raadsma · 2010 · BMC Bioinformatics
59. Binomial Mixture Model‐based Association Tests under Genetic Heterogeneity
    Hui Zhou, Wei Pan · 2009 · Annals of Human Genetics
60. Linkage mapping of the locus for inherited ovine arthrogryposis (IOA) to sheep Chromosome 5
    Angela M. Murphy, David Evan MacHugh, Stephen D. E. Park · 2007 · Mammalian Genome
61. Association between temperament in terms of the Regulative Theory of Temperament and DRD4 and DAT1 gene polymorphisms
    Włodzimierz Oniszczenko, Wojciech Łukasz Dragan · 2012 · Comprehensive Psychiatry
62. Haplotype Counting for Sensitive Chimerism Testing
    Marija Debeljak, Evelina Mocci, Max C. Morrison, Aparna Pallavajjalla, Katie F. Beierl, Marie Amiel, Michaël Noë, Laura DeLong Wood, Ming‐Tseh Lin, Christopher D. Gocke et al. · 2017 · Journal of Molecular Diagnostics
63. Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families
    Ellen M. Wijsman, Joseph H. Rothstein, Robert P. Igo, John D. Brunzell, Arno G. Motulsky, Gail Pairitz Jarvik · 2010 · Human Genetics
64. Analysis of heterogeneity and epistasis in physiological mixed populations by combined structural equation modelling and latent class analysis
    Mogens Fenger, Allan R Linneberg, Thomas Mears Werge, Torben Jørgensen · 2008 · BMC Genetics
65. Using disease symptoms to improve detection of linkage under genetic heterogeneity
    Alexandre Bureau, Aurélie Labbe, Jordie Croteau, Chantal Mérette · 2008 · Genetic Epidemiology
66. Importance sampling-based estimation over AND/OR search spaces for graphical models
    Vibhav Gogate, Rina Dechter · 2012 · Artificial Intelligence
67. Genetic variation and forensic efficiency of autosomal insertion/deletion polymorphisms in Chinese Bai ethnic group: phylogenetic analysis to other populations
    Chun-Hua Yang, Caiyong Yin, Chunmei Shen et al. · 2017 · Oncotarget
68. Linkage analysis identifies novel genetic modifiers of microbiome traits in families with inflammatory bowel disease
    Arunabh Sharma, Silke Szymczak, Malte Christoph Rühlemann, Sandra Freitag‐Wolf, Carolin Knecht, Janna Enderle, Stefan Schreiber, André Franke, Wolfgang Lieb, Michael Krawczak et al. · 2022 · Gut Microbes
69. Correlational structure of ‘frontal’ tests and intelligence tests indicates two components with asymmetrical neurostructural correlates in old age
    Simon R. Cox, Sarah E. MacPherson, Karen J. Ferguson, Jack J. Nissan, Natalie A. Royle, Alasdair M. J. MacLullich, Joanna Marguerite Wardlaw, Ian J. Deary · 2014 · Intelligence
70. Quantitative Trait Loci Affecting Response to Crowding Stress in an F2 Generation of Rainbow Trout Produced Through Phenotypic Selection
    Caird E. Rexroad, Roger L. Vallejo, Sixin Liu · 2013 · Marine Biotechnology
71. Bone marrow-derived epithelial cells and hair follicle stem cells contribute to development of chronic cutaneous neoplasms
    Heuijoon Park, Sonali Lad, Kelsey Boland et al. · 2018 · Nature Communications
72. Unsupervised quantitative methods to analyze student reasoning lines: Theoretical aspects and examples
    Onofrio Rosario Battaglia, Benedetto Di Paola, Claudio Fazio · 2019 · Physical Review Physics Education Research
73. A linkage search for joint panic disorder/bipolar genes
    Mark W. Logue, Martina Durner, Gary A. Heiman · 2009 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
74. Design and Implementation of a Twin-Family Database for Behavior Genetics and Genomics Studies
    Dorret Irene Boomsma, Gonneke A. H. M. Willemsen, Jacqueline M. Vink et al. · 2008 · Twin Research and Human Genetics
75. Statistical tools for linkage analysis and genetic association studies
    P. Forabosco, M. Falchi, M. Devoto · 2005 · Expert Review of Molecular Diagnostics
76. Theoretical strategies for high-resolution mapping of complex genetic disorders in humans
    Zewei Luo, Rongmei Zhang · 1999 · Chinese Science Bulletin
77. An Immunoglobulin Switchlike Sequence Is Linked With Canine Narcolepsy
    Emmanuel Jean-Marie Mignot, R. A. Bell, C. Rattazzi · 1994 · SLEEP
78. Power comparison between population-based case-control studies and family-based transmission-disequilibrium tests: An empirical study
    Saurabh Ghosh, Tanushree Haldar · 2011 · Indian journal of human genetics
79. Likelihood Ratio Testing for Admixture Models with Application to Genetic Linkage Analysis
    Chongzhi Di, Kung‐Yee Liang · 2011 · Biometrics
80. Absence of association of a polymorphic GGC repeat at the 5′ untranslated region of the reelin gene with schizophrenia
    Chia-Hsing Huang, Chia‐Hsiang Chen · 2006 · Psychiatry Research
81. Homozygosity Mapping on Homozygosity Haplotype Analysis to Detect Recessive Disease-Causing Genes from a Small Number of Unrelated, Outbred Patients
    Koichi Hagiwara, Hiroyuki Morino, Jun Shiihara · 2011 · PLoS ONE
82. A parallel genetic algorithm to discover patterns in genetic markers that indicate predisposition to multifactorial disease
    Tobias Rausch, Alun Thomas, Nicola J. Camp · 2008 · Computers in Biology and Medicine
83. Principles for the organization of gene-sets
    Wentian Li, Jan Freudenberg, Michaela Oswald · 2015 · Computational Biology and Chemistry
84. Exploiting gene × gene interaction in linkage analysis
    Yungui Huang, Christopher W. Bartlett, Alberto M. Segre · 2007 · BMC Proceedings
85. Analysis of Polymorphism of the Number of Tandem Repeats in the Aggrecan Gene Exon G3 in the Families with Idiopathic Scoliosis
    Irina V. Zorkoltseva, O. A. Lubinsky, Ruslan Sharipov · 2002 · Russian Journal of Genetics
86. The Genetic Epidemiology of Growth and Development
    Bradford Towne, Ellen W. Demerath, Stefan A. Czerwinski · 2002 · Elsevier eBooks
87. Further evidence for linkage of low–mid frequency hearing impairment to the candidate region on chromosome 4p16.3
    S Brodwolf, IR Böddeker, Andreas Ziegler · 2001 · Clinical Genetics
88. Presymptomatic Diagnosis of Nonsyndromic Hearing Loss by Genotyping
    Achih H. Chen, Robert F. Mueller, Sai D. Prasad · 1998 · Archives of Otolaryngology - Head and Neck Surgery
89. Standardization of a SNP panel for parentage verification and identification in the domestic cat (Felis silvestris catus)
    M. de Groot, Heidi Anderson, H. Bauer, C. Bauguil, Rebecca R. Bellone, R. Brugidou, Reuben M. Buckley, Peter Dovč, Oliver P. Forman, Robert A. Grahn et al. · 2021 · Animal Genetics
90. In silico whole-genome EST analysis reveals 2322 novel microsatellites for the silver-lipped pearl oyster, Pinctada maxima
    David B. Jones, Kyall Richard Zenger, Dean Robert Jerry · 2011 · Marine Genomics
91. Design considerations in a sib-pair study of linkage for susceptibility loci in cancer
    Richard A. Kerber, Christopher Ian Amos, Beow Yong Yeap, Dianne M. Finkelstein, Duncan C. Thomas · 2008 · BMC Medical Genetics
92. Testing homogeneity in discrete mixtures
    Richard Charnigo, Jiayang Sun · 2007 · Journal of Statistical Planning and Inference
93. Semiparametric Inference in a Genetic Mixture Model
    Pengfei Li, Yukun Liu, Jing Qin · 2016 · Journal of the American Statistical Association
94. Power of pedigree likelihood analysis in extended pedigrees to classify rare variants of uncertain significance in cancer risk genes
    Elisabeth A. Rosenthal, John Michael O. Rañola, Brian H. Shirts · 2017 · Familial Cancer
95. Prevalence and inheritance of hip osteoarthritis in Iceland
    Þorvaldur Ingvarsson · 2001 · Acta Orthopaedica Scandinavica
96. The Complexity of Checking Consistency of Pedigree Information and Related Problems
    Luca Aceto, Jens Alsted Hansen, Anna Ingólfsdóttir · 2003 · BRICS Report Series
97. Molecular Genetics of Schizophrenia
    Peter McGuffin, Michael J. Owen, Michael Gill · 1992 · Springer eBooks
98. Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program
    Jason M. Laramie, Jemma B. Wilk, Steven C. Hunt · 2006 · BMC Medical Genetics
99. A comparison of methods for intermediate fine mapping
    Charalampos Papachristou, Shili Lin · 2006 · Genetic Epidemiology
100. No association between common variations in the human alpha 2 subunit gene (ATP1A2) of the sodium–potassium-transporting ATPase and idiopathic generalized epilepsy
     Falk W. Lohoff, Thomas N. Ferraro, Thomas Sander · 2005 · Neuroscience Letters