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Simultaneous localization of two linked disease susceptibility genesBIERNACKA, Joanna M; LEI SUN; BULL, Shelley B et al.Genetic epidemiology. 2005, Vol 28, Num 1, pp 33-47, issn 0741-0395, 15 p.Article

Conditional multipoint linkage analysis using affected sib pairs: An alternative approachCHIU, Yen-Feng; LIANG, Kung-Yee.Genetic epidemiology. 2004, Vol 26, Num 2, pp 108-115, issn 0741-0395, 8 p.Article

Identity-by-descent analysis of sibship configurations when parental haplotypes can be distinguishedSHUTE, N. C. E.American journal of medical genetics. 1988, Vol 29, Num 2, pp 425-429, issn 0148-7299Article

A simulation-based analysis of chromosome segment sharing among a group of arbitrarily related individualsLIBIGER, Ondrej; SCHORK, Nicholas J.European journal of human genetics. 2007, Vol 15, Num 12, pp 1260-1268, issn 1018-4813, 9 p.Article

A multimarker regression-based test of linkage for affected sib-pairs at two linked lociBARBER, Mathew J; TODD, John A; CORDELL, Heather J et al.Genetic epidemiology. 2006, Vol 30, Num 3, pp 191-208, issn 0741-0395, 18 p.Article

A Monte Carlo approach to calculating probabilities for continuous identity by descent dataBROWNING, Sharon.Journal of applied probability. 2000, Vol 37, Num 3, pp 850-864, issn 0021-9002Article

Introduction of the IBD information into the Weighted Pairwise Correlation method for linkage analysisZINN-JUSTIN, A; ABEL, L.Genetic epidemiology. 1999, Vol 17, Num 1, pp 35-50, issn 0741-0395Article

Multipoint affected sibpair linkage methods for localizing susceptibility genes of complex diseasesGLIDDEN, David V; LIANG, Kung-Yee; CHIU, Yen-Feng et al.Genetic epidemiology. 2003, Vol 24, Num 2, pp 107-117, issn 0741-0395, 11 p.Article

Clinical Genetics and the Hutterite Population : A Review of Mendelian DisordersBOYCOTT, Kym M; PARBOOSINGH, Jillian S; MOLLER, Lisbeth Birk et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 8, pp 1088-1098, issn 1552-4825, 11 p.Article

Tests for the presence of two linked disease susceptibility genesBIERNACKA, Joanna M; LEI SUN; BULL, Shelley B et al.Genetic epidemiology. 2005, Vol 29, Num 4, pp 389-401, issn 0741-0395, 13 p.Article

Genomic mismatch scanning identifies human genomic DNA shared identical by descentCHEUNG, V. G; NELSON, S. F.Genomics (San Diego, Calif.). 1998, Vol 47, Num 1, pp 1-6, issn 0888-7543Article

Novel Autosomal Recessive Malformation Syndrome ssociated With Developmental Delay and Distinctive Facies Maps to 16ptel in the Hutterite PopulationBOYCOTT, Kym M; BEAULIEU, Chandree; PUFFENBERGER, Erik G et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 6, pp 1349-1356, issn 1552-4825, 8 p.Article

Introductory guide to the statistics of molecular genetics : Molecular geneticsELEY, Thalia C; RIJSDIJK, Frühling.Journal of child psychology and psychiatry and allied disciplines (Print). 2005, Vol 46, Num 10, pp 1042-1044, issn 0021-9630, 3 p.Article

Power of multipoint identity-by-descent methods to detect linkage using variance component modelsEKSTRØM, Claus Thorn.Genetic epidemiology. 2001, Vol 21, Num 4, pp 285-298, issn 0741-0395Article

Linkage-disequilibrium mapping without genotypingCHEUNG, V. G; GREGG, J. P; NELSON, S. F et al.Nature genetics. 1998, Vol 18, Num 3, pp 225-230, issn 1061-4036Article

Testing linkage and gene x environment interaction: Comparison of different affected sib-pair methodsDIZIER, M. H; SELINGER-LENEMAN, H; GENIN, E et al.Genetic epidemiology. 2003, Vol 25, Num 1, pp 73-79, issn 0741-0395, 7 p.Article

Haplotype kinship for three populations of the Goettingen minipigFLURY, Christine; WEIGEND, Steffen; DING, Xiangdong et al.Genetics selection evolution (Print). 2007, Vol 39, Num 2, pp 159-179, issn 0999-193X, 21 p.Article

Fuzzy p-values in latent variable problemsTHOMPSON, Elizabeth A; GEYER, Charles J.Biometrika. 2007, Vol 94, Num 1, pp 49-60, issn 0006-3444, 12 p.Article

Phenotypic and Genetic Analysis of a Large Family With Migraine-Associated VertigoLEE, Hane; JEN, Joanna C; CHA, Yoon-Hee et al.Headache. 2008, Vol 48, Num 10, pp 1460-1467, issn 0017-8748, 8 p.Article

Prediction of IBD based on population history for fine gene mappingHERNANDEZ-SANCHEZ, Jules; HALEY, Chris S; WOOLLIAMS, John A et al.Genetics selection evolution (Print). 2006, Vol 38, Num 3, pp 231-252, issn 0999-193X, 22 p.Article

A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disordersINNES, A. M; BOYCOTT, K. M; PARBOOSINGH, J. S et al.Clinical genetics. 2010, Vol 78, Num 5, pp 424-431, issn 0009-9163, 8 p.Article

QTL detection and allelic effects for growth and fat traits in outbred pig populationsNAGAMINE, Yoshitaka; VISSCHER, Peter M; HALEY, Chris S et al.Genetics selection evolution (Print). 2004, Vol 36, Num 1, pp 83-96, issn 0999-193X, 14 p.Article

Using DNA Fingerprints to Infer Familial Relationships Within NHANES III HouseholdsKATKI, Hormuzd A; SANDERS, Christopher L; GRAUBARD, Barry I et al.Journal of the American Statistical Association. 2010, Vol 105, Num 490, pp 552-563, issn 0162-1459, 12 p.Article

High-Resolution Identity by Descent Mapping Uncovers the Genetic Basis for Blood Pressure Differences Between Spontaneously Hypertensive Rat LinesBELL, Rebecca; HERRING, Stacy M; GOKUL, Nisha et al.Circulation. Cardiovascular genetics (Print). 2011, Vol 4, Num 3, pp 223-231, issn 1942-325X, 9 p.Article

New Algorithms for Evaluating the Log-Likelihood Function Derivatives in the AI-REML MethodMISHCHENKO, Kateryna; NEYTCHEVA, Maya.Communications in statistics. Simulation and computation. 2009, Vol 38, Num 6-7, pp 1348-1364, issn 0361-0918, 17 p.Article

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