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Frontiers in genetics, ISSN 1664-8021, 2013, Volume 4, p. 59
The increased feasibility of whole-genome (or whole-exome) sequencing has led to renewed interest in using family data to find disease mutations. For clinical... 
MCMC | Epistasis | genome-wide association | linkage analysis | PPL | Linkage Disequilibrium
Journal Article
Journal Article
Human Genetics, ISSN 0340-6717, 2/2015, Volume 134, Issue 2, pp. 191 - 201
Journal Article
American Journal of Medical Genetics - Neuropsychiatric Genetics, ISSN 1552-4841, 07/2001, Volume 105, Issue 5, pp. 406 - 413
Journal Article
American Journal of Psychiatry, ISSN 0002-953X, 04/2009, Volume 166, Issue 4, pp. 434 - 441
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2003, Volume 73, Issue 6, pp. 1471 - 1473
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 04/2005, Volume 76, Issue 4, p. 688
Results of autism linkage studies have been difficult to interpret across research groups, prompting the use of ever-increasing sample sizes to increase power.... 
Autism | Genetic linkage | Genetics
Journal Article
by Anney, Richard J.L and Kenny, Elaine M and O'Dushlaine, Colm and Yaspan, Brian L and Parkhomenka, Elena and Buxbaum, Joseph D and Sutcliffe, James and Gill, Michael and Gallagher, Louise and Bailey, Anthony J and Fernandez, Bridget A and Szatmari, Peter and Scherer, Stephen W and Patterson, Andrew and Marshall, Christian R and Pinto, Dalila and Vincent, John B and Fombonne, Eric and Betancur, Catalina and Delorme, Richard and Leboyer, Marion and Bourgeron, Thomas and Mantoulan, Carine and Roge, Bernadette and Tauber, Mäité and Freitag, Christine M and Poustka, Fritz and Duketis, Eftichia and Klauck, Sabine M and Poustka, Annemarie and Papanikolaou, Katerina and Tsiantis, John and Bolshakova, Nadia and Brennan, Sean and Hughes, Gillian and McGrath, Jane and Merikangas, Alison and Ennis, Sean and Green, Andrew and Casey, Jillian P and Conroy, Judith M and Regan, Regina and Shah, Naisha and Maestrini, Elena and Bacchelli, Elena and Minopoli, Fiorella and Stoppioni, Vera and Battaglia, Agatino and Igliozzi, Roberta and Parrini, Barbara and Tancredi, Raffaella and Oliveira, Guiomar and Almeida, Joana and Duque, Frederico and Vicente, Astrid and Correia, Catarina and Magalhaes, Tiago R and Gillberg, Christopher and Nygren, Gudrun and De Jonge, Maretha and Van Engeland, Herman and Vorstman, Jacob A.S and Wittemeyer, Kerstin and Baird, Gillian and Bolton, Patrick F and Rutter, Michael L and Green, Jonathan and Lamb, Janine A and Pickles, Andrew and Parr, Jeremy R and Le Couteur, Ann and Berney, Tom and McConachie, Helen and Wallace, Simon and Coutanche, Marc and Foley, Suzanne and White, Kathy and Monaco, Anthony P and Holt, Richard and Farrar, Penny and Pagnamenta, Alistair T and Mirza, Ghazala K and Ragoussis, Jiannis and Sousa, Inês and Sykes, Nuala and Wing, Kirsty and Hallmayer, Joachim and Cantor, Rita M and Nelson, Stanley F and Geschwind, Daniel H and Abrahams, Brett S and Volkmar, Fred and Pericak-Vance, Margaret A and Cuccaro, Michael L and Gilbert, John and Cook, Edwin H and Guter, Stephen J and Jacob, Suma and Nurnberger, John I and McDougle, Christopher J and ... and Autism Genome Project and The Autism Genome Project
European Journal of Human Genetics, ISSN 1018-4813, 10/2011, Volume 19, Issue 10, pp. 1082 - 1089
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2008, Volume 82, Issue 6, pp. 1349 - 1356
We report here a preliminary model of the genetic architecture of Autoimmune Thyroid Disorder (AITD). Using a flexible class of mathematical modeling... 
POSTERIOR PROBABILITY | FAMILIES | DISEASE | THYROGLOBULIN | GENETICS & HEREDITY | ASCERTAINMENT |