Search Results - "Human heredity" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Violation of the Constant Genetic Effect Assumption Can Result in Biased Estimates for Non-Linear Mendelian Randomization

Violation of the Constant Genetic Effect Assumption Can Result in Biased Estimates for Non-Linear Mendelian Randomization

by Burgess, Stephen
Published in Human heredity (01.01.2023)

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Journal Article

Power and Sample Size Calculations for Genetic Association Studies in the Presence of Genetic Model Misspecification

Power and Sample Size Calculations for Genetic Association Studies in the Presence of Genetic Model Misspecification

by Moore, Camille M., Jacobson, Sean A., Fingerlin, Tasha E.
Published in Human heredity (2019)

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Journal Article

The kinship2 R Package for Pedigree Data

The kinship2 R Package for Pedigree Data

by Sinnwell, Jason P., Therneau, Terry M., Schaid, Daniel J.
Published in Human heredity (01.01.2014)

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Likelihood-Based Association Analysis for Nuclear Families and Unrelated Subjects with Missing Genotype Data

Likelihood-Based Association Analysis for Nuclear Families and Unrelated Subjects with Missing Genotype Data

by Dudbridge, Frank
Published in Human heredity (01.01.2008)

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A Data-Adaptive Sum Test for Disease Association with Multiple Common or Rare Variants

A Data-Adaptive Sum Test for Disease Association with Multiple Common or Rare Variants

by Han, Fang, Pan, Wei
Published in Human heredity (01.01.2010)

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Comprehensive Assessment of Genotype Imputation Performance

Comprehensive Assessment of Genotype Imputation Performance

by Shi, Shuo, Yuan, Na, Yang, Ming, Du, Zhenglin, Wang, Jinyue, Sheng, Xin, Wu, Jiayan, Xiao, Jingfa
Published in Human heredity (2018)

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A statistical testing strategy accounting for random and non-random (skewed) X-chromosome inactivation identifies lung cancer susceptibility loci among smokers

A statistical testing strategy accounting for random and non-random (skewed) X-chromosome inactivation identifies lung cancer susceptibility loci among smokers

by Jantzen, Rodolphe, Camilleri-Broët, Sophie, Ezer, Nicole, Broët, Philippe
Published in Human heredity (14.06.2024)

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Two Novel Variants of the CAPN3 Gene in Chinese Patients with Limb-Girdle Muscular Dystrophy Recessive 1

Two Novel Variants of the CAPN3 Gene in Chinese Patients with Limb-Girdle Muscular Dystrophy Recessive 1

by Zhang, Lulu, Zhang, Yi, Han, Chunru, Jiang, Juean, Jiang, Jianhua, Cai, Xiuying, Yu, Liqiang, Qi, Huan, Fang, Qi, Ding, Dongxue
Published in Human heredity (05.06.2024)

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comorbidPGS: An R Package Assessing Shared Predisposition between Phenotypes Using Polygenic Scores

comorbidPGS: An R Package Assessing Shared Predisposition between Phenotypes Using Polygenic Scores

by Pascat, Vincent, Zudina, Liudmila, Ulrich, Anna, Maina, Jared G., Kaakinen, Marika, Pupko, Igor, Bonnefond, Amélie, Demirkan, Ayse, Balkhiyarova, Zhanna, Froguel, Philippe, Prokopenko, Inga
Published in Human heredity (13.05.2024)

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Place of Concordance-Discordance Model in Evaluating Next-Generation Sequencing Performance

Place of Concordance-Discordance Model in Evaluating Next-Generation Sequencing Performance

by Zhai, Yue, Bardel, Claire, Vallée, Maxime, Iwaz, Jean, Roy, Pascal
Published in Human heredity (16.03.2024)

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Implications of the Co-Dominance Model for Hardy-Weinberg Testing in Genetic Association Studies

Implications of the Co-Dominance Model for Hardy-Weinberg Testing in Genetic Association Studies

by Wellek, Stefan, Mueller-Nurasyid, Martina, Strauch, Konstantin
Published in Human heredity (02.03.2024)

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Implications of the Codominance Model for Hardy-Weinberg Testing in Genetic Association Studies

Implications of the Codominance Model for Hardy-Weinberg Testing in Genetic Association Studies

by Wellek, Stefan, Müller-Nurasyid, Martina, Strauch, Konstantin
Published in Human heredity (02.03.2024)

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A Statistical Testing Strategy Accounting for Random and Nonrandom (Skewed) X-Chromosome Inactivation Identifies Lung Cancer Susceptibility Loci among Smokers

A Statistical Testing Strategy Accounting for Random and Nonrandom (Skewed) X-Chromosome Inactivation Identifies Lung Cancer Susceptibility Loci among Smokers

by Jantzen, Rodolphe, Camilleri-Broët, Sophie, Ezer, Nicole, Broët, Philippe
Published in Human heredity (01.01.2024)

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Journal Article

Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer

Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer

by Brugger, Markus, Lutz, Manuel, Müller-Nurasyid, Martina, Lichtner, Peter, Slater, Emily P., Matthäi, Elvira, Bartsch, Detlef K., Strauch, Konstantin
Published in Human heredity (01.01.2024)

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Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants

Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants

by Curtis, David
Published in Human heredity (01.01.2024)

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The Diagnostic Value of miR-124a Expression in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis

The Diagnostic Value of miR-124a Expression in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis

by Wu, Tianhao, Zhang, Yanlong, Peng, Aqin, Wu, Xirui
Published in Human heredity (01.01.2023)

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A Comprehensive Study of Disease-Causing Variants in PAH, QDPR, PTS, and PCD Genes in Iranian Patients with Hyperphenylalaninemia: A Systematic Review

A Comprehensive Study of Disease-Causing Variants in PAH, QDPR, PTS, and PCD Genes in Iranian Patients with Hyperphenylalaninemia: A Systematic Review

by Ghanei, Mahmoud, Sadat Fatemi, Seyedeh Helia, Hamzehlouei, Tayebeh
Published in Human heredity (16.01.2023)

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A Novel PMVK Variant Associated with Familial Porokeratosis

A Novel PMVK Variant Associated with Familial Porokeratosis

by Zhang, Wenjing, Nie, Xinmiao, Shi, Lei, Shao, Fengmin, Cao, Lihua
Published in Human heredity (01.01.2023)

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A Common Variant of ARRB2 Promoter Region Associated with the Prognosis of Heart Failure

A Common Variant of ARRB2 Promoter Region Associated with the Prognosis of Heart Failure

by Ren, Hongqiang, liu, Yijun, Tan, Zhen, Luo, Guiquan, Zhang, Mei, Li, Shuang, Tang, Tingwei, Zhao, Li
Published in Human heredity (01.01.2023)

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Journal Article

Methods and Software to Analyze Gene-Environment Interactions under a Case-Mother-Control-Mother Design with Partially Missing Child Genotype

Methods and Software to Analyze Gene-Environment Interactions under a Case-Mother-Control-Mother Design with Partially Missing Child Genotype

by Bureau, Alexandre, Tian, Yuang, Levallois, Patrick, Giguère, Yves, Chen, Jinbo, Zhang, Hong
Published in Human heredity (01.01.2023)

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