نتایج جستجو برای: homozygosity mapping

تعداد نتایج: 200921  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2016
Aziz Belkadi Vincent Pedergnana Aurélie Cobat Yuval Itan Quentin B Vincent Avinash Abhyankar Lei Shang Jamila El Baghdadi Aziz Bousfiha Alexandre Alcais Bertrand Boisson Jean-Laurent Casanova Laurent Abel

Principal component analysis (PCA), homozygosity rate estimations, and linkage studies in humans are classically conducted through genome-wide single-nucleotide variant arrays (GWSA). We compared whole-exome sequencing (WES) and GWSA for this purpose. We analyzed 110 subjects originating from different regions of the world, including North Africa and the Middle East, which are poorly covered by...

Journal: :Genetic epidemiology 1997
S W Guo

Homozygosity mapping is a very powerful method for mapping rare recessive diseases in humans. In many applications, it is often desirable to compute prior (or unconditional) multilocus probability of autozygosity for inbred pedigrees. This paper proposes a simple yet powerful method for computing the prior multilocus autozygosity probability for complex inbred pedigrees. The method has an added...

Journal: :Archives of disease in childhood 1999
J P Shield E J Wadsworth T J Hassold L A Judis P A Jacobs

AIMS To examine the age of onset of insulin dependent diabetes mellitus (IDDM) in children with Down's syndrome compared with non-trisomic individuals, and to assess whether differences might be related to disomic homozygosity at the autoimmune polyglandular disease type 1 (APECED) gene locus. METHODS Children with Down's syndrome and IDDM were identified through the Down's syndrome associati...

2015
Sundaramurthy Srilekha Tharigopala Arokiasamy Natarajan N. Srikrupa Vetrivel Umashankar Swaminathan Meenakshi Parveen Sen Suman Kapur Nagasamy Soumittra Dror Sharon

Leber congenital amaurosis (LCA) and retinitis pigmentosa (RP) are retinal degenerative diseases which cause severe retinal dystrophy affecting the photoreceptors. LCA is predominantly inherited as an autosomal recessive trait and contributes to 5% of all retinal dystrophies; whereas RP is inherited by all the Mendelian pattern of inheritance and both are leading causes of visual impairment in ...

2017
Carlos A. Pantoja-Melendez Antonio Miranda-Duarte Bladimir Roque-Ramirez Juan C. Zenteno

Limb-Girdle Muscular Dystrophy type 2 (LGMD2) is a group of autosomally recessive inherited disorders defined by weakness and wasting of the shoulder and pelvic girdle muscles. In the past, several population isolates with high incidence of LGMD2 arising from founder mutation effects have been identified. The aim of this work is to describe the results of clinical, epidemiologic, and molecular ...

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