Literature DB >> 27124789

Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden.

Mohamed Abouelhoda1,2, Turki Sobahy1,2, Mohamed El-Kalioby1,2, Nisha Patel1, Hanan Shamseldin1, Dorota Monies1,2, Nada Al-Tassan1,2, Khushnooda Ramzan1, Faiqa Imtiaz1, Ranad Shaheen1, Fowzan S Alkuraya1,2,3.   

Abstract

BACKGROUND: Most autosomal recessive diseases are rare, but they collectively account for a substantial proportion of disease burden, especially in consanguineous populations. Estimation of this disease burden, however, is hampered by many factors, including lack of countrywide registries. Establishing carrier frequency can be a practical surrogate to estimate disease burden, although the requirement of a large representative cohort may be challenging.
PURPOSE: We propose that the application of clinical genomics in the diagnostic setting offers a unique opportunity to estimate carrier frequency in the population as a secondary benefit.
METHODS: We used a data set of ~7,100 patients who underwent genomic testing for various Mendelian disorders to estimate the carrier frequency.
RESULTS: We were able to calculate the frequency of 259 confirmed founder recessive mutations. We found the corresponding disease burden to be, at minimum, ~7 per 1,000 children born to first-cousin parents, with disorders related to intellectual disability and vision impairment being the most common.
CONCLUSION: Our approach can be utilized to inform the design of new policies for the prevention of genetic disorders and highlights an important secondary benefit of clinical genomics.Genet Med 18 12, 1244-1249.

Entities:  

Mesh:

Year:  2016        PMID: 27124789     DOI: 10.1038/gim.2016.37

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  33 in total

1.  Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield.

Authors:  S Anazi; S Maddirevula; E Faqeih; H Alsedairy; F Alzahrani; H E Shamseldin; N Patel; M Hashem; N Ibrahim; F Abdulwahab; N Ewida; H S Alsaif; H Al Sharif; W Alamoudi; A Kentab; F A Bashiri; M Alnaser; A H AlWadei; M Alfadhel; W Eyaid; A Hashem; A Al Asmari; M M Saleh; A AlSaman; K A Alhasan; M Alsughayir; M Al Shammari; A Mahmoud; Z N Al-Hassnan; M Al-Husain; R Osama Khalil; N Abd El Meguid; A Masri; R Ali; T Ben-Omran; P El Fishway; A Hashish; A Ercan Sencicek; M State; A M Alazami; M A Salih; N Altassan; S T Arold; M Abouelhoda; S M Wakil; D Monies; R Shaheen; F S Alkuraya
Journal:  Mol Psychiatry       Date:  2016-07-19       Impact factor: 15.992

2.  Warsaw breakage syndrome: Further clinical and genetic delineation.

Authors:  Ebba Alkhunaizi; Ranad Shaheen; Sanjay Kumar Bharti; Ann M Joseph-George; Karen Chong; Ghada M H Abdel-Salam; Mohammed Alowain; Susan I Blaser; Blake C Papsin; Mohammed Butt; Mais Hashem; Nicole Martin; Ruth Godoy; Robert M Brosh; Fowzan S Alkuraya; David Chitayat
Journal:  Am J Med Genet A       Date:  2018-09-14       Impact factor: 2.802

3.  Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.

Authors:  Dorota Monies; Mohammed Abouelhoda; Mirna Assoum; Nabil Moghrabi; Rafiullah Rafiullah; Naif Almontashiri; Mohammed Alowain; Hamad Alzaidan; Moeen Alsayed; Shazia Subhani; Edward Cupler; Maha Faden; Amal Alhashem; Alya Qari; Aziza Chedrawi; Hisham Aldhalaan; Wesam Kurdi; Sameena Khan; Zuhair Rahbeeni; Maha Alotaibi; Ewa Goljan; Hadeel Elbardisy; Mohamed ElKalioby; Zeeshan Shah; Hibah Alruwaili; Amal Jaafar; Ranad Albar; Asma Akilan; Hamsa Tayeb; Asma Tahir; Mohammed Fawzy; Mohammed Nasr; Shaza Makki; Abdullah Alfaifi; Hanna Akleh; Suad Yamani; Dalal Bubshait; Mohammed Mahnashi; Talal Basha; Afaf Alsagheir; Musad Abu Khaled; Khalid Alsaleem; Maisoon Almugbel; Manal Badawi; Fahad Bashiri; Saeed Bohlega; Raashida Sulaiman; Ehab Tous; Syed Ahmed; Talal Algoufi; Hamoud Al-Mousa; Emadia Alaki; Susan Alhumaidi; Hadeel Alghamdi; Malak Alghamdi; Ahmed Sahly; Shapar Nahrir; Ali Al-Ahmari; Hisham Alkuraya; Ali Almehaidib; Mohammed Abanemai; Fahad Alsohaibaini; Bandar Alsaud; Rand Arnaout; Ghada M H Abdel-Salam; Hasan Aldhekri; Suzan AlKhater; Khalid Alqadi; Essam Alsabban; Turki Alshareef; Khalid Awartani; Hanaa Banjar; Nada Alsahan; Ibraheem Abosoudah; Abdullah Alashwal; Wajeeh Aldekhail; Sami Alhajjar; Sulaiman Al-Mayouf; Abdulaziz Alsemari; Walaa Alshuaibi; Saeed Altala; Abdulhadi Altalhi; Salah Baz; Muddathir Hamad; Tariq Abalkhail; Badi Alenazi; Alya Alkaff; Fahad Almohareb; Fuad Al Mutairi; Mona Alsaleh; Abdullah Alsonbul; Somaya Alzelaye; Shakir Bahzad; Abdulaziz Bin Manee; Ola Jarrad; Neama Meriki; Bassem Albeirouti; Amal Alqasmi; Mohammed AlBalwi; Nawal Makhseed; Saeed Hassan; Isam Salih; Mustafa A Salih; Marwan Shaheen; Saadeh Sermin; Shamsad Shahrukh; Shahrukh Hashmi; Ayman Shawli; Ameen Tajuddin; Abdullah Tamim; Ahmed Alnahari; Ibrahim Ghemlas; Maged Hussein; Sami Wali; Hatem Murad; Brian F Meyer; Fowzan S Alkuraya
Journal:  Am J Hum Genet       Date:  2019-05-23       Impact factor: 11.025

4.  ASHG 2020 Curt Stern Award introduction: Fowzan Sami Alkuraya.

Authors:  Cynthia C Morton
Journal:  Am J Hum Genet       Date:  2021-03-04       Impact factor: 11.025

5.  How the human genome transformed study of rare diseases.

Authors:  Fowzan S Alkuraya
Journal:  Nature       Date:  2021-02       Impact factor: 49.962

6.  Report of a Second Lebanese Family with Basel-Vanagaite-Smirin-Yosef Syndrome: Possible Founder Mutation.

Authors:  Pratibha Nair; Sandra Sabbagh; Sami Bizzari; Florian Brunner; Samantha Stora; Mahmoud T Al-Ali; Martin Gencik; Stephany El-Hayek; André Mégarbané
Journal:  Mol Syndromol       Date:  2019-06-28

7.  2020 Curt Stern Award address: a more perfect clinical genome-how consanguineous populations contribute to the medical annotation of the human genome.

Authors:  Fowzan S Alkuraya
Journal:  Am J Hum Genet       Date:  2021-03-04       Impact factor: 11.025

8.  Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome.

Authors:  Nina Mann; Slim Mzoughi; Ronen Schneider; Susanne J Kühl; Denny Schanze; Verena Klämbt; Svjetlana Lovric; Youying Mao; Shasha Shi; Weizhen Tan; Michael Kühl; Ana C Onuchic-Whitford; Ernestine Treimer; Thomas M Kitzler; Franziska Kause; Sven Schumann; Makiko Nakayama; Florian Buerger; Shirlee Shril; Amelie T van der Ven; Amar J Majmundar; Kristina Marie Holton; Amy Kolb; Daniela A Braun; Jia Rao; Tilman Jobst-Schwan; Eva Mildenberger; Thomas Lennert; Alma Kuechler; Dagmar Wieczorek; Oliver Gross; Beate Ermisch-Omran; Anja Werberger; Martin Skalej; Andreas R Janecke; Neveen A Soliman; Shrikant M Mane; Richard P Lifton; Jan Kadlec; Ernesto Guccione; Michael J Schmeisser; Martin Zenker; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2021-02-16       Impact factor: 10.121

9.  The prevalence, genetic complexity and population-specific founder effects of human autosomal recessive disorders.

Authors:  Qingyang Xiao; Volker M Lauschke
Journal:  NPJ Genom Med       Date:  2021-06-02       Impact factor: 8.617

10.  An Early Diagnostic Clue for COL18A1- and LAMA1-Associated Diseases: High Myopia With Alopecia Areata in the Cranial Midline.

Authors:  Panfeng Wang; Xiaoyun Jia; Xueshan Xiao; Shiqiang Li; Yuxi Long; Mengchu Liu; Yongyu Li; Jun Li; Yan Xu; Qingjiong Zhang
Journal:  Front Cell Dev Biol       Date:  2021-06-25
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