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Linkage analysis

Gene selection tool (GST): A R-based tool for genetic disorders based on the sliding-window proportion test using whole-exome sequencing data

Sugi Lee, Minah Jung, Jaeeun Jung, Kunhyang Park, Jea-Woon Ryu, Jeongkil Kim, Dae-soo Kim

published 28 Sep 2017

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Accurate phenotyping: Reconciling approaches through Bayesian model averaging

Carla Chia-Ming Chen, Jonathan Macgregor Keith, Kerrie Lee Mengersen

published 19 Apr 2017

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A Genome-Wide SNP Linkage Analysis Suggests a Susceptibility Locus on 6p21 for Ankylosing Spondylitis and Inflammatory Back Pain Trait

Yanli Zhang, Zetao Liao, Qiujing Wei, Yunfeng Pan, Xinwei Wang, Shuangyan Cao, Zishi Guo, Yuqiong Wu, Ju Rong, Ou Jin, Manlong Xu, Zhiming Lin, Jieruo Gu

published 14 Dec 2016

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Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts

Bushra Irum, Shahid Y. Khan, Muhammad Ali, Haiba Kaul, Firoz Kabir, Bushra Rauf, Fareeha Fatima, Raheela Nadeem, Arif O. Khan, Saif Al Obaisi, Muhammad Asif Naeem, Idrees A. Nasir, Shaheen N. Khan, Tayyab Husnain, Sheikh Riazuddin, Javed Akram, Allen O. Eghrari, S. Amer Riazuddin

published 04 Nov 2016

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Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families

Hiroko Okuda, Atsuko Noguchi, Hatasu Kobayashi, Daiki Kondo, Kouji H. Harada, Shohab Youssefian, Hirotomo Shioi, Risako Kabata, Yuki Domon, Kazufumi Kubota, Yutaka Kitano, Yasunori Takayama, Toshiaki Hitomi, Kousaku Ohno, Yoshiaki Saito, Takeshi Asano, Makoto Tominaga, Tsutomu Takahashi, Akio Koizumi

published 25 May 2016

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Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

Beate Peter, Ellen M. Wijsman, Alejandro Q. Nato Jr., University of Washington Center for Mendelian Genomics , Mark M. Matsushita, Kathy L. Chapman, Ian B. Stanaway, John Wolff, Kaori Oda, Virginia B. Gabo, Wendy H. Raskind

published 27 Apr 2016

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Creative Activities in Music – A Genome-Wide Linkage Analysis

Jaana Oikkonen, Tuire Kuusi, Petri Peltonen, Pirre Raijas, Liisa Ukkola-Vuoti, Kai Karma, Päivi Onkamo, Irma Järvelä

published 24 Feb 2016

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Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome

Kaihui Zhang, Shu Liu, Bing Feng, Yali Yang, Haiyan Zhang, Rui Dong, Yi Liu, Zhongtao Gai

published 03 Feb 2016

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Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing

Dennis Lal, Bernd A. Neubauer, Mohammad R. Toliat, Janine Altmüller, Holger Thiele, Peter Nürnberg, Clemens Kamrath, Anne Schänzer, Thomas Sander, Andreas Hahn, Michael Nothnagel

published 20 Jan 2016

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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

published 11 Jan 2016

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The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families

Behzad Davarniya, Hao Hu, Kimia Kahrizi, Luciana Musante, Zohreh Fattahi, Masoumeh Hosseini, Fariba Maqsoud, Reza Farajollahi, Thomas F. Wienker, H. Hilger Ropers, Hossein Najmabadi

published 26 Aug 2015

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Viral Genetic Linkage Analysis in the Presence of Missing Data

Shelley H. Liu, Gabriel Erion, Vladimir Novitsky, Victor De Gruttola

published 24 Aug 2015

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A Major Gene for Bovine Ovulation Rate

Brian W. Kirkpatrick, Chris A. Morris

published 05 Jun 2015

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