The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.
Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report
Open accessAbstract
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.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“This will bias the results if, as seems plausible, consanguineous marriages tend to occur in families with a tradition of close-kin unions (Hussain and Bittles 2000; Hamamy et al. 2011).”
From An Estimate of the Average Number of Recessive Lethal Mutations Carried by Humans (2015) · cites this paper as Hamamy et al. 2011
In the citing paper
“This prediction agrees well with the estimated 3.5 -4.4% increased risk for prereproductive mortality and 1.7 -2.8% increased incidence of congenital anomalies in children of first cousins above the general population risk (Hamamy et al. 2011).”
From An Estimate of the Average Number of Recessive Lethal Mutations Carried by Humans (2015) · cites this paper as Hamamy et al. 2011
In the citing paper
“Over the past centuries, consanguineous marriages were a common practice, and the custom remains prevalent in many countries (Bittles and Black 2010a; Hamamy et al. 2011).”
From An Estimate of the Average Number of Recessive Lethal Mutations Carried by Humans (2015) · cites this paper as Hamamy et al. 2011
Citations
Cites
Consanguinity, human evolution, and complex diseases
Bittles, A. H., & Black, M. L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906079106 · Cited by 646
Self-citationConsanguinity and reproductive health among Arabs
Tadmouri, G. O., Nair, P., Obeid, T., Ali, M. T. A., Khaja, N. A., & Hamamy, H. (2009) · Reproductive Health · doi:10.1186/1742-4755-6-17 · Cited by 642
Self-citationConsanguinity and its relevance to clinical genetics
Bittles, A. H. (2001) · Clinical Genetics · doi:10.1034/j.1399-0004.2001.600201.x · Cited by 602
Self-citationReproductive Behavior and Health in Consanguineous Marriages
Bittles, A. H., Mason, W. M., Greene, J., & Rao, N. A. (1991) · Science · doi:10.1126/science.2028254 · Cited by 331
Self-citationMutations in PYCR1 cause cutis laxa with progeroid features
Reversade, B., Escande‐Beillard, N., Dimopoulou, A., Fischer‐Zirnsak, B., Chng, S. C., Li, Y., Shboul, M., Tham, P.-Y., Kayserili, H., Al‐Gazali, L., et al. (2009) · Nature Genetics · doi:10.1038/ng.413 · Cited by 262
Self-citationBennett, R. L., Motulsky, A. G., Bittles, A. H., Hudgins, L., Uhrich, S. B., Doyle, D. L., Silvey, K., Scott, C. R., Cheng, E., McGillivray, B., et al. (2002) · Journal of Genetic Counseling · doi:10.1023/a:1014593404915 · Cited by 234
Self-citationConsanguineous marriage in Jordan
Khoury, S., & Massad, D. (1992) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320430502 · Cited by 219
Genetic Disorders Among Arab Populations
Teebi, A. S. (2010) · Springer eBooks · doi:10.1007/978-3-642-05080-0 · Cited by 162
CONSANGUINEOUS MARRIAGE IN A NEWLY DEVELOPED COUNTRY: THE QATARI POPULATION
Bener, A., & Alali, K. (2004) · Journal of Biosocial Science · doi:10.1017/s0021932004007060 · Cited by 160
Contribution of BRCA1 and BRCA2 Mutations to Breast and Ovarian Cancer in Pakistan
Liede, A., Malik, I. A., Aziz, Z., Rios, P. D. L., Kwan, E., & Narod, S. A. (2002) · The American Journal of Human Genetics · doi:10.1086/342506 · Cited by 159
Temtamy, S. A., & Aglan, M. S. (2008) · Orphanet Journal of Rare Diseases · doi:10.1186/1750-1172-3-15 · Cited by 158
Self-citationCONSANGUINITY IN LEBANON: PREVALENCE, DISTRIBUTION AND DETERMINANTS
Barbour, B., & Salameh, P. (2009) · Journal of Biosocial Science · doi:10.1017/s0021932009003290 · Cited by 144
Jurdi, R., & Saxena, P. C. (2002) · Journal of Biosocial Science · doi:10.1017/s0021932003000014 · Cited by 144
Consanguineous marriages in Jordan: why is the rate changing with time?
Hamamy, H. A., Jamhawi, L., Al‐Darawsheh, J., & Ajlouni, K. M. (2005) · Clinical Genetics · doi:10.1111/j.1399-0004.2005.00426.x · Cited by 141
Self-citationIdentification of multiple loci for Alzheimer disease in a consanguineous Israeli-Arab community
Farrer, L. A. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddg037 · Cited by 133
The impact of consanguinity on neonatal and infant health.
Bittles, A. H., & Black, M. L. (2010) · Early Human Development · doi:10.1016/j.earlhumdev.2010.08.003 · Cited by 132
Self-citationConsanguinity in a population sample of Israeli Muslim Arabs, Christian Arabs and Druze
Vardi-Saliternik, R., Friedlander, Y., & Cohen, T. (2002) · Annals of Human Biology · doi:10.1080/03014460110100928 · Cited by 119
Consanguineous marriage and congenital heart defects: A case‐control study in the neonatal period
Yunis, K. A., Mumtaz, G. R., Fadi, B., Chamseddine, F., May, K., Joseph, R., Makhoul, G., & Hala, T. (2006) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.31309 · Cited by 92
Consanguinity, inbreeding, and genetic drift in Italy
Cavalli-Sforza, L. L., Moroni, A., & Zei, G. (2004) · Cited by 86
Self-citationMendelian disorders and multifactorial traits: the big divide or one for all?
Antonarakis, S. E., Chakravarti, A., Cohen, J. C., & Hardy, J. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2793 · Cited by 85
Self-citationCONSANGUINITY IN QATAR: KNOWLEDGE, ATTITUDE AND PRACTICE IN A POPULATION BORN BETWEEN 1946 AND 1991
Sandridge, A. L., TAKEDDIN, J., Al-KAABI, E. H., & Frances, Y.-M. (2009) · Journal of Biosocial Science · doi:10.1017/s002193200999023x · Cited by 85
CONSANGUINITY TRENDS AND CORRELATES IN THE PALESTINIAN TERRITORIES
Assaf, S., & Khawaja, M. (2008) · Journal of Biosocial Science · doi:10.1017/s0021932008002940 · Cited by 80
PREVALENCE OF CONSANGUINEOUS MARRIAGES IN SYRIA
Othman, H., & Saadat, M. (2009) · Journal of Biosocial Science · doi:10.1017/s0021932009003411 · Cited by 80
Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE)
Al‐Gazali, L., & Ali, B. R. (2010) · Human Mutation · doi:10.1002/humu.21232 · Cited by 79
A recent survey of consanguineous marriages in Japan
Imaizumi, Y. (1986) · Clinical Genetics · doi:10.1111/j.1399-0004.1986.tb00600.x · Cited by 68
Consanguineous marriages in Beirut: Time trends, spatial distribution
Khlat, M. (1988) · Biodemography and Social Biology · doi:10.1080/19485565.1988.9988710 · Cited by 60
Jordan: Communities and Community Genetics
Hamamy, H., Al-Hait, S., Alwan, A., & Ajlouni, K. M. (2006) · Public Health Genomics · doi:10.1159/000096282 · Cited by 60
Self-citationAldahmesh, M. A., Abu‐Safieh, L., Khan, A. O., Al‐Hassnan, Z. N., Shaheen, R., Rajab, M., Monies, D., Meyer, B. F., & Alkuraya, F. S. (2009) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.32753 · Cited by 55
Temtamy, S. A., Aglan, M., Valencia, M., Cocchi, G., Pacheco, M., Ashour, A. M., Amr, K. S., Helmy, S. M. H., Gammal, M. E., Wright, M., et al. (2008) · Human Mutation · doi:10.1002/humu.20778 · Cited by 54
Self-citationFamilial aggregation, the PDE4D gene, and ischemic stroke in a genetically isolated population
van Rijn, M. J. E., Slooter, A. J. C., Schut, A. F., Isaacs, A. J., Aulchenko, Y. S., Snijders, P. J. L. M., Kappelle, L. J., Swieten, J. C. V., Oostra, B. A., & van Duijn, C. M. (2005) · Neurology · doi:10.1212/01.wnl.0000178744.42953.b7 · Cited by 49
Consanguinity, Genetic Drift, and Genetic Diseases in Populations with Reduced Numbers of Founders
Bittles, A. H. (2009) · Springer eBooks · doi:10.1007/978-3-540-37654-5_19 · Cited by 48
Self-citationDoes consanguinity lead to decreased incidence of breast cancer?
Bener, A., El-Ayoubi, H. R., Ali, A. I., Al-Kubaisi, A., & Al‐Sulaiti, H. (2010) · Cancer Epidemiology · doi:10.1016/j.canep.2010.04.004 · Cited by 42
Culture and Acculturation Influences on Palestinian Perceptions of Prenatal Genetic Counseling
Awwad, R. I., Veach, P. M., Bartels, D. M., & LeRoy, B. S. (2007) · Journal of Genetic Counseling · doi:10.1007/s10897-007-9131-2 · Cited by 41
Self-citationZlotogora, J., & Shalev, S. A. (2010) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.33537 · Cited by 41
Self-citationGrjibovski, A. M., Magnus, P. M., & Stoltenberg, C. (2009) · Scandinavian Journal of Public Health · doi:10.1177/1403494808100939 · Cited by 36
Negotiating Risk: British Pakistani Experiences of Genetics
Shaw, A. (2009) · Cited by 35
Self-citationThe molecular basis of autosomal recessive diseases among the Arabs and Druze in Israel
Zlotogora, J. (2010) · Human Genetics · doi:10.1007/s00439-010-0890-8 · Cited by 33
Self-citationBennett, R. L., Hudgins, L., Smith, C. O., & Motulsky, A. G. (1999) · Genetics in Medicine · doi:10.1097/00125817-199909000-00007 · Cited by 32
Self-citationRelatives as spouses: Preferences and opportunities for kin marriage in a Western society
Bras, H. A. J., van Poppel, F. W. A., & Mandemakers, K. (2009) · American Journal of Human Biology · doi:10.1002/ajhb.20896 · Cited by 32
Collaborative genomics for human health and cooperation in the Mediterranean region
Özçelık, T., Kanaan, M. N., Avraham, K. B., Yannoukakos, D., Mégarbané, A., Tadmouri, G. O., Middleton, L. T., Romeo, G., King, M., & Levy‐Lahad, E. (2010) · Nature Genetics · doi:10.1038/ng0810-641 · Cited by 29
Self-citationDobrusin, M., Weitzman, D., Levine, J., Kremer, I., Rietschel, M., Maier, W., & Belmaker, R. H. (2009) · The World Journal of Biological Psychiatry · doi:10.3109/15622970701849960 · Cited by 27
Ignoring Distant Genealogic Loops Leads to False‐positives in Homozygosity Mapping
Liu, F., Elefante, S., van Duijn, C. M., & Aulchenko, Y. S. (2006) · Annals of Human Genetics · doi:10.1111/j.1469-1809.2006.00279.x · Cited by 26
Inbreeding effects in the epigenetic era
Biémont, C. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2664-c1 · Cited by 25
Consanguinity Mapping of Congenital Heart Disease in a South Indian Population
Mcgregor, T. L., Misri, A., Bartlett, J., Orabona, G., Friedman, R. D., Sexton, D., Maheshwari, S., & Morgan, T. M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010286 · Cited by 22
Teeuw, M. E., Henneman, L., Bochdanovits, Z., Heutink, P., Kuik, D. J., Cornel, M. C., & ten Kate, L. P. (2010) · BMC Medical Genetics · doi:10.1186/1471-2350-11-113 · Cited by 22
Self-citationten Kate, L. P., Teeuw, M. E., Henneman, L., & Cornel, M. C. (2010) · Journal of Community Genetics · doi:10.1007/s12687-010-0002-4 · Cited by 17
Self-citationMégarbané, A., Dorison, N., Rodriguez, D., & Tamraz, J. C. (2010) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.33417 · Cited by 16
Inbreeding and epigenetics: beneficial as well as deleterious effects
Nebert, D. W., Gálvez‐Peralta, M., Shi, Z., & Dragin, N. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2664-c2 · Cited by 13
Welberg, L. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2926 · Cited by 3
Romeo, G. (2010) · Human Mutation · doi:10.1002/humu.21369 · Cited by 3
Self-citationConsanguinity, inbreeding and genetic drift in Italy. Monographs in population biology 39
Pollak, E. (2004) · American Journal of Human Biology · doi:10.1002/ajhb.20085 · Cited by 2
Research works printed but not linked: 1
- Geneva International Consanguinity Workshop. 2010. Available at: http://www.medecine.unige.ch/consanguinity/. Accessed December 1, 2010.
Cited by
Sorted by citations
Hamamy, H. (2011) · Journal of Community Genetics · doi:10.1007/s12687-011-0072-y · Cited by 456
Self-citationSheridan, E. G., Wright, J., Small, N., Corry, P. C., Oddie, S., Whibley, C., Petherick, E., Malik, T., Pawson, N., McKinney, P. A., et al. (2013) · The Lancet · doi:10.1016/s0140-6736(13)61132-0 · Cited by 255
Rehder, C. W., David, K. L., Hirsch, B. A., Toriello, H. V., Wilson, C. M., & Kearney, H. M. (2013) · Genetics in Medicine · doi:10.1038/gim.2012.169 · Cited by 158
Carrier screening for recessive disorders
Antonarakis, S. E. (2019) · Nature Reviews Genetics · doi:10.1038/s41576-019-0134-2 · Cited by 134
Self-citationGenetics of consanguinity and inbreeding in health and disease
Fareed, M., & Afzal, M. (2016) · Annals of Human Biology · doi:10.1080/03014460.2016.1265148 · Cited by 128
Metadata
- Authors
- Hamamy, H., Antonarakis, S. E., Cavalli-Sforza, L. L., Temtamy, S., Romeo, G., Ten Kate, L. P., Bennett, R. L., Shaw, A., Megarbane, A., van Duijn, C., Bathija, H., Fokstuen, S., Engel, E., Zlotogora, J., Dermitzakis, E., Bottani, A., Dahoun, S., Morris, M. A., Arsenault, S., Aglan, M. S., Ajaz, M., Alkalamchi, A., Alnaqeb, D., Alwasiyah, M. K., Anwer, N., Awwad, R., Bonnefin, M., Peter Corry, M. D., Gwanmesia, L., Karbani, G. A., Mostafavi, M., Pippucci, T., Ranza-Boscardin, E., Reversade, B., Sharif, S. M., Teeuw, M. E., & Bittles, A. H.
- Affiliations
- University of Geneva (CH)
- University of Pavia (IT)
- National Research Centre (EG)
- University of Bologna (IT)
- Amsterdam UMC Location Vrije Universiteit Amsterdam (NL)
- University of Washington Medical Center (US)
- University of Oxford (GB)
- Erasmus MC (NL)
- World Health Organization (CH)
- University Hospital of Geneva (CH)
- Génome Québec (CA)
- University of Bedfordshire (GB)
- Ministry of Health (IQ)
- King Saud University (SA)
- Baghdad Medical City (IQ)
- Hadassah Medical Center (IL)
- King's College London (GB)
- Leeds Teaching Hospitals NHS Trust (GB)
- IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola (IT)
- Agency for Science, Technology and Research (SG)
- Chapel Allerton Hospital (GB)
- Amsterdam Public Health (NL)
- Edith Cowan University (AU)
- Corresponding author
- Hamamy, Hanan
- ORCID
- Venue
- Genetics in Medicine
- Publisher
- Elsevier BV
- Published
- 2011-09
- Volume
- 13
- Issue
- 9
- Pages
- 841-847
- ISSN
- 1098-3600 (ISSN-L)
- OpenAlex
- W2062921444
- Cited by
- 345
- References
- 51
- Citations by year
- 2026: 22 · 2025: 28 · 2024: 27 · 2023: 28 · 2022: 18 · 2021: 31 · 2020: 25 · 2019: 23 · 2018: 23 · 2017: 17 · 2016: 24 · 2015: 21 · 2014: 30 · 2013: 11 · 2012: 14
- FWCI
- 61.91
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Genetics in Medicine (publishedVersion)
- PubMed (publishedVersion)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- Archive ouverte UNIGE (University of Geneva) (publishedVersion)
- Murdoch University Research Portal (submittedVersion)
- Australasian Journal of Paramedicine (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- Digital Academic REpository of VU University Amsterdam (Vrije Universiteit Amsterdam) (submittedVersion)
- Pure Amsterdam UMC (submittedVersion)
- Archive ouverte UNIGE (University of Geneva) (submittedVersion, cc-by)
- Topics
- Social Sciences › Sociology and Political Science › Marriage and Family Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Keywords
- consanguineous marriage, cousin marriage, autozygosity, inbreeding depression, genetic counseling, genotype-phenotype correlation, copy number variation, immigrant communities
- MeSH terms
- Consanguinity, Disease, Female, Humans, Male, Marriage, Quantitative Trait, Heritable, Genetic Research, DNA Copy Number Variations
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review