نتایج جستجو برای: homozygosity mapping

تعداد نتایج: 200921  

2009
Maleeha Azam Muhammad Imran Khan Andreas Gal Alamdar Hussain Syed Tahir Abbas Shah Muhammad Shakil Khan Ahmed Sadeque Habib Bokhari Rob W.J. Collin Ulrike Orth Maria M. van Genderen A.I. den Hollander Frans P. M. Cremers Raheel Qamar

PURPOSE To identify the gene mutations responsible for autosomal recessive retinitis pigmentosa (arRP) in Pakistani families. METHODS A cohort of consanguineous families with typical RP phenotype in patients was screened by homozygosity mapping using microsatellite markers that mapped close to 21 known arRP genes and five arRP loci. Mutation analysis was performed by direct sequencing of the ...

2012
M J Soltani Banavandi K Kahrizi F Behjati M Mohseni H Darvish I Bahman S S Abedinni S Ghasemi Firouzabadi E Jafari Sh Ghadami F Sabbagh Gh R Kavoosi H Najmabadi

BACKGROUND Intellectual disability (ID) has a worldwide prevalence of 1-3% and results from extraordinary heterogeneous. To shed more light on the causes of ID in Kerman Province, in Southeast Iran, we set out in 2008 to perform systematic clinical studies and homozygosity mapping in large Iranian families with ID. METHODS Fifty seven families with a minimum of two mentally retarded children ...

2012
Samer Khateb Lina Zelinger Tamar Ben-Yosef Saul Merin Ornit Crystal-Shalit Menachem Gross Eyal Banin Dror Sharon

We used a combined approach of homozygosity mapping and whole exome sequencing (WES) to search for the genetic cause of autosomal recessive retinitis pigmentosa (arRP) in families of Yemenite Jewish origin. Homozygosity mapping of two arRP Yemenite Jewish families revealed a few homozygous regions. A subsequent WES analysis of the two index cases revealed a shared homozygous novel nucleotide de...

2010
Ines Pereiro Diana Valverde Teresa Piñeiro-Gallego Montserrat Baiget Salud Borrego Carmen Ayuso Charles Searby Darryl Nishimura

PURPOSE Bardet-Biedl syndrome (BBS, OMIM 209900) is a rare multi-organ disorder in which BBS patients manifest a variable phenotype that includes retinal dystrophy, polydactyly, mental delay, obesity, and also reproductive tract and renal abnormalities. Mutations in 14 genes (BBS1-BBS14) are found in 70% of the patients, indicating that additional mutations in known and new BBS genes remain to ...

Journal: :Investigative ophthalmology & visual science 2011
Rob W J Collin L Ingeborgh van den Born B Jeroen Klevering Marta de Castro-Miró Karin W Littink Kentar Arimadyo Maleeha Azam Volkan Yazar Marijke N Zonneveld Codrut C Paun Anna M Siemiatkowska Tim M Strom Jayne Y Hehir-Kwa Hester Y Kroes Jan-Tjeerd H N de Faber Mary J van Schooneveld John R Heckenlively Carel B Hoyng Anneke I den Hollander Frans P M Cremers

PURPOSE To determine the genetic defects underlying autosomal recessive retinitis pigmentosa (arRP) in the Dutch population and in a subset of patients originating from other countries. The hypothesis was that, because there has been little migration over the past centuries in certain areas of The Netherlands, a significant fraction of Dutch arRP patients carry their genetic defect in the homoz...

Journal: :American journal of human genetics 2008
Ruth McQuillan Anne-Louise Leutenegger Rehab Abdel-Rahman Christopher S Franklin Marijana Pericic Lovorka Barac-Lauc Nina Smolej-Narancic Branka Janicijevic Ozren Polasek Albert Tenesa Andrew K Macleod Susan M Farrington Pavao Rudan Caroline Hayward Veronique Vitart Igor Rudan Sarah H Wild Malcolm G Dunlop Alan F Wright Harry Campbell James F Wilson

Estimating individual genome-wide autozygosity is important both in the identification of recessive disease variants via homozygosity mapping and in the investigation of the effects of genome-wide homozygosity on traits of biomedical importance. Approaches have tended to involve either single-point estimates or rather complex multipoint methods of inferring individual autozygosity, all on the b...

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