Literature DB >> 23208456

Consanguinity, endogamy, and genetic disorders in Tunisia.

Nizar Ben Halim1, Nissaf Ben Alaya Bouafif, Lilia Romdhane, Rym Kefi Ben Atig, Ibtissem Chouchane, Yosra Bouyacoub, Imen Arfa, Wafa Cherif, Sonia Nouira, Faten Talmoudi, Khaled Lasram, Sana Hsouna, Welid Ghazouani, Hela Azaiez, Leila El Matri, Abdelmajid Abid, Neji Tebib, Marie-Françoise Ben Dridi, Salem Kachboura, Ahlem Amouri, Mourad Mokni, Saida Ben Arab, Koussay Dellagi, Sonia Abdelhak.   

Abstract

Entities:  

Year:  2012        PMID： 23208456      PMCID： PMC3666836          DOI： 10.1007/s12687-012-0128-7

Source DB:  PubMed          Journal:  J Community Genet        ISSN： 1868-310X


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  86 in total

Review 1.  Does inbreeding lead to decreased human fertility?

Authors:  A H Bittles; J C Grant; S G Sullivan; R Hussain
Journal:  Ann Hum Biol       Date:  2002 Mar-Apr       Impact factor: 1.533

2.  Inbreeding: Disease susceptibility in California sea lions.

Authors:  Karina Acevedo-Whitehouse; Frances Gulland; Denise Greig; William Amos
Journal:  Nature       Date:  2003-03-06       Impact factor: 49.962

3.  Inbreeding and risk of late onset complex disease.

Authors:  I Rudan; D Rudan; H Campbell; A Carothers; A Wright; N Smolej-Narancic; B Janicijevic; L Jin; R Chakraborty; R Deka; P Rudan
Journal:  J Med Genet       Date:  2003-12       Impact factor: 6.318

4.  Inbreeding and susceptibility to osteoporosis in Croatian island isolates.

Authors:  Igor Rudan; Tatjana Skarić-Jurić; Nina Smolej-Narancić; Branka Janićijević; Diana Rudan; Irena Martinović Klarić; Lovorka Barać; Marijana Pericić; Radoslav Galić; Margaret Lethbridge-Cejku; Pavao Rudan
Journal:  Coll Antropol       Date:  2004-12

5.  Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia.

Authors:  Todd Lencz; Christophe Lambert; Pamela DeRosse; Katherine E Burdick; T Vance Morgan; John M Kane; Raju Kucherlapati; Anil K Malhotra
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-05       Impact factor: 11.205

6.  Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.

Authors:  C Geoffrey Woods; James Cox; Kelly Springell; Daniel J Hampshire; Moin D Mohamed; Martin McKibbin; Rowena Stern; F Lucy Raymond; Richard Sandford; Saghira Malik Sharif; Gulshan Karbani; Mustaq Ahmed; Jacquelyn Bond; David Clayton; Chris F Inglehearn
Journal:  Am J Hum Genet       Date:  2006-03-21       Impact factor: 11.025

7.  Consanguinity and early mortality in the Muslim populations of India and Pakistan.

Authors:  R Hussain; A H Bittles; S Sullivan
Journal:  Am J Hum Biol       Date:  2001 Nov-Dec       Impact factor: 1.937

8.  Founder mutations and the high prevalence of myotonia congenita in northern Finland.

Authors:  H Papponen; T Toppinen; P Baumann; V Myllylä; J Leisti; H Kuivaniemi; G Tromp; R Myllylä
Journal:  Neurology       Date:  1999-07-22       Impact factor: 9.910

9.  The probability of consanguineous marriages.

Authors:  L L Cavalli-Sforza; M Kimura; I Barrai
Journal:  Genetics       Date:  1966-07       Impact factor: 4.562

10.  Estimating human inbreeding coefficients: comparison of genealogical and marker heterozygosity approaches.

Authors:  A D Carothers; I Rudan; I Kolcic; O Polasek; C Hayward; A F Wright; H Campbell; P Teague; N D Hastie; J L Weber
Journal:  Ann Hum Genet       Date:  2006-09       Impact factor: 1.670
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  16 in total

1.  Clinical and genetic study of Tunisian families with genetic generalized epilepsy: contribution of CACNA1H and MAST4 genes.

Authors:  Zied Landoulsi; Fatma Laatar; Eric Noé; Saloua Mrabet; Mouna Ben Djebara; Guillaume Achaz; Caroline Nava; Stéphanie Baulac; Imen Kacem; Amina Gargouri-Berrechid; Riadh Gouider; Eric Leguern
Journal:  Neurogenetics       Date:  2018-06-12       Impact factor: 2.660

2.  Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes.

Authors:  Leila Youssefian; Hassan Vahidnezhad; Amir Hossein Saeidian; Soheila Sotoudeh; Hamidreza Mahmoudi; Maryam Daneshpazhooh; Nessa Aghazadeh; Rebecca Adams; Alireza Ghanadan; Sirous Zeinali; Paolo Fortina; Jouni Uitto
Journal:  Eur J Hum Genet       Date:  2017-09-06       Impact factor: 4.246

3.  Update of the spectrum of mucopolysaccharidoses type III in Tunisia: identification of three novel mutations and in silico structural analysis of the missense mutations.

Authors:  Souad Ouesleti; Maria Francisca Coutinho; Isaura Ribeiro; Abdehedi Miled; Dalila Saidane Mosbahi; Sandra Alves
Journal:  World J Pediatr       Date:  2017-01-19       Impact factor: 2.764

4.  Clinical and genetic characteristics of Tunisian children with infantile nephropathic cystinosis.

Authors:  Mariem El Younsi; Médiha Trabelsi; Sandra Ben Youssef; Inès Ouertani; Yousra Hammi; Ahlem Achour; Faouzi Maazoul; Maher Kharrat; Tahar Gargah; Ridha M'rad
Journal:  Pediatr Nephrol       Date:  2022-04-20       Impact factor: 3.714

5.  Stillbirth Among Arab Women in Canada, 1981-2015.

Authors:  Nathalie Auger; Judith Racape; Marie-France Raynault; Marianne Bilodeau-Bertrand; Ga Eun Lee; Teresa Janevic
Journal:  Public Health Rep       Date:  2020-01-22       Impact factor: 2.792

6.  A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients.

Authors:  Khaoula Ben-Farhat; Imen Ben-Mustapha; Meriem Ben-Ali; Karen Rouault; Saber Hamami; Najla Mekki; Amel Ben-Chehida; Beya Larguèche; Zohra Fitouri; Selim Abdelmoula; Monia Khemiri; Mohamed-Neji Guediche; Samir Boukthir; Sihem Barsaoui; Jalel Chemli; Mohamed-Ridha Barbouche
Journal:  J Clin Immunol       Date:  2016-05-25       Impact factor: 8.317

Review 7.  Lessons from Genetic Studies of Primary Immunodeficiencies in a Highly Consanguineous Population.

Authors:  Mohamed-Ridha Barbouche; Najla Mekki; Meriem Ben-Ali; Imen Ben-Mustapha
Journal:  Front Immunol       Date:  2017-06-27       Impact factor: 7.561

8.  Particular Mal de Meleda phenotypes in Tunisia and mutations founder effect in the Mediterranean region.

Authors:  Mbarka Bchetnia; Nadia Laroussi; Monia Youssef; Cherine Charfeddine; Ahlem Sabrine Ben Brick; Mohamed Samir Boubaker; Mourad Mokni; Sonia Abdelhak; Jameleddine Zili; Rym Benmously
Journal:  Biomed Res Int       Date:  2013-09-04       Impact factor: 3.411

9.  Further evidence of mutational heterogeneity of the XPC gene in Tunisian families: a spectrum of private and ethnic specific mutations.

Authors:  Mariem Ben Rekaya; Manel Jerbi; Olfa Messaoud; Ahlem Sabrine Ben Brick; Mohamed Zghal; Chiraz Mbarek; Ashraf Chadli-Debbiche; Meriem Jones; Mourad Mokni; Hamouda Boussen; Mohamed Samir Boubaker; Becima Fazaa; Houda Yacoub-Youssef; Sonia Abdelhak
Journal:  Biomed Res Int       Date:  2013-07-25       Impact factor: 3.411

10.  Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.

Authors:  Bashayer Al-Mubarak; Mohamed Abouelhoda; Aisha Omar; Hesham AlDhalaan; Mohammed Aldosari; Michael Nester; Hussain A Alshamrani; Mohamed El-Kalioby; Ewa Goljan; Renad Albar; Shazia Subhani; Asma Tahir; Sultana Asfahani; Alaa Eskandrani; Ahmed Almusaiab; Amna Magrashi; Jameela Shinwari; Dorota Monies; Nada Al Tassan
Journal:  Sci Rep       Date:  2017-07-18       Impact factor: 4.379
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