TY - GEN
T1 - Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report
AU - Hamamy, Hanan
AU - Antonarakis, Stylianos E.
AU - Cavalli-Sforza, Luigi Luca
AU - Temtamy, Samia
AU - Romeo, Giovanni
AU - Kate, Leo P.Ten
AU - Bennett, Robin L.
AU - Shaw, Alison
AU - Megarbane, Andre
AU - Van Duijn, Cornelia
AU - Bathija, Heli
AU - Fokstuen, Siv
AU - Engel, Eric
AU - Zlotogora, Joel
AU - Dermitzakis, Emmanouil
AU - Bottani, Armand
AU - Dahoun, Sophie
AU - Morris, Michael A.
AU - Arsenault, Steve
AU - Aglan, Mona S.
AU - Ajaz, Mubasshir
AU - Alkalamchi, Ayad
AU - Alnaqeb, Dhekra
AU - Alwasiyah, Mohamed K.
AU - Anwer, Nawfal
AU - Awwad, Rawan
AU - Bonnefin, Melissa
AU - Corry, Peter
AU - Gwanmesia, Lorraine
AU - Karbani, Gulshan A.
AU - Mostafavi, Maryam
AU - Pippucci, Tommaso
AU - Ranza-Boscardin, Emmanuelle
AU - Reversade, Bruno
AU - Sharif, Saghira M.
AU - Teeuw, Marieke E.
AU - Bittles, Alan H.
N1 - Generated from Scopus record by KAUST IRTS on 2023-02-15
PY - 2011/9/1
Y1 - 2011/9/1
N2 - Approximately 1.1 billion people currently live in countries where consanguineous marriages are customary, and among them one in every three marriages is between cousins. Opinions diverge between those warning of the possible health risks to offspring and others who highlight the social benefits of consanguineous marriages. A consanguinity study group of international experts and counselors met at the Geneva International Consanguinity Workshop from May 3 2010, to May 7, 2010, to discuss the known and presumptive risks and benefits of close kin marriages and to identify important future areas for research on consanguinity. The group highlighted the importance of evidence-based counseling recommendations for consanguineous marriages and of undertaking both genomic and social research in defining the various influences and outcomes of consanguinity. Technological advances in rapid high-throughput genome sequencing and for the identification of copy number variants by comparative genomic hybridization offer a significant opportunity to identify genotype-phenotype correlations focusing on autozygosity, the hallmark of consanguinity. The ongoing strong preferential culture of close kin marriages in many societies, and among migrant communities in Western countries, merits an equivalently detailed assessment of the social and genetic benefits of consanguinity in future studies. © 2011 Lippincott Williams &Wilkins.
AB - Approximately 1.1 billion people currently live in countries where consanguineous marriages are customary, and among them one in every three marriages is between cousins. Opinions diverge between those warning of the possible health risks to offspring and others who highlight the social benefits of consanguineous marriages. A consanguinity study group of international experts and counselors met at the Geneva International Consanguinity Workshop from May 3 2010, to May 7, 2010, to discuss the known and presumptive risks and benefits of close kin marriages and to identify important future areas for research on consanguinity. The group highlighted the importance of evidence-based counseling recommendations for consanguineous marriages and of undertaking both genomic and social research in defining the various influences and outcomes of consanguinity. Technological advances in rapid high-throughput genome sequencing and for the identification of copy number variants by comparative genomic hybridization offer a significant opportunity to identify genotype-phenotype correlations focusing on autozygosity, the hallmark of consanguinity. The ongoing strong preferential culture of close kin marriages in many societies, and among migrant communities in Western countries, merits an equivalently detailed assessment of the social and genetic benefits of consanguinity in future studies. © 2011 Lippincott Williams &Wilkins.
UR - https://linkinghub.elsevier.com/retrieve/pii/S1098360021036480
UR - http://www.scopus.com/inward/record.url?scp=80052606841&partnerID=8YFLogxK
U2 - 10.1097/GIM.0b013e318217477f
DO - 10.1097/GIM.0b013e318217477f
M3 - Conference contribution
SP - 841
EP - 847
BT - Genetics in Medicine
ER -