Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report

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

Consanguinity 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

Consanguinity and its relevance to clinical genetics

Bittles, A. H. (2001) · Clinical Genetics · doi:10.1034/j.1399-0004.2001.600201.x · Cited by 602

Reproductive Behavior and Health in Consanguineous Marriages

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Mutations 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

Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors

Bennett, 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

Consanguineous marriage in Jordan

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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

Consanguineous marriages

Hamamy, H. (2011) · Journal of Community Genetics · doi:10.1007/s12687-011-0072-y · Cited by 456

Risk factors for congenital anomaly in a multiethnic birth cohort: an analysis of the Born in Bradford study

Sheridan, 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

American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing

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

Genetics 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

An Estimate of the Average Number of Recessive Lethal Mutations Carried by Humans

Gao, Z., Waggoner, D., Stephens, M., Ober, C., & Przeworski, M. (2015) · Genetics · doi:10.1534/genetics.114.173351 · Cited by 109

Consanguinity, endogamy, and genetic disorders in Tunisia

Halim, N. B., Alaya, N. B. B., Romdhane, L., Kéfi, R., Chouchane, I., Bouyacoub, Y., Arfa, I., Cherif, W., Nouira, S., Talmoudi, F., et al. (2012) · Journal of Community Genetics · doi:10.1007/s12687-012-0128-7 · Cited by 109

Ancient DNA reveals admixture history and endogamy in the prehistoric Aegean

Skourtanioti, E., Ringbauer, H., Gnecchi‐Ruscone, G. A., Bianco, R. A., Burri, M., Freund, C., Furtwängler, A., Martins, N. F. G., Knolle, F., Neumann, G. U., et al. (2023) · Nature Ecology & Evolution · doi:10.1038/s41559-022-01952-3 · Cited by 106

Effects of consanguinity in a cohort of subjects with certain genetic disorders in Qatar

Ben‐Omran, T., Al-Ghanim, K. A., Yavarna, T., Akoum, M. E., Samara, M. M., Chandra, P., & Al-Dewik, N. I. E. (2019) · Molecular Genetics & Genomic Medicine · doi:10.1002/mgg3.1051 · Cited by 102

A multicenter clinical exome study in unselected cohorts from a consanguineous population of Saudi Arabia demonstrated a high diagnostic yield

Alfares, A. A., Alfadhel, M., Wani, T. A., Alsahli, S., Alluhaydan, I., Mutairi, F. A., Alothaim, A., Balwi, M. A. A., Alsubaie, L., Al-Turki, S., et al. (2017) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2017.04.002 · Cited by 98

Αlpha-thalassemia: A practical overview

Musallam, K. M., Cappellini, M. D., Coates, T. D., Kuo, K. H. M., Al-Samkari, H. T., Sheth, S., Viprakasit, V., & Taher, A. T. (2024) · Blood Reviews · doi:10.1016/j.blre.2023.101165 · Cited by 104

National surveillance for type 1, type 2 diabetes and prediabetes among children and adolescents: a population-based study (SAUDI-DM)

Al-Rubeaan, K. A. (2015) · Journal of Epidemiology & Community Health · doi:10.1136/jech-2015-205710 · Cited by 92

Diagnostic Exome Sequencing to Elucidate the Genetic Basis of Likely Recessive Disorders in Consanguineous Families

Makrythanasis, P., Nelis, M., Santoni, F. A., Guipponi, M., Vannier, A., Béna, F., Gimelli, S., Stathaki, E., Temtamy, S. A., Mégarbané, A., et al. (2014) · Human Mutation · doi:10.1002/humu.22617 · Cited by 87

Consanguinity and Dysmorphology in Arabs

Al‐Gazali, L., & Hamamy, H. (2014) · Human Heredity · doi:10.1159/000360421 · Cited by 86

Genetics and genomics in Brazil: a promising future

Passos‐Bueno, M. R., Bertola, D. R., Horovitz, D. D. G., Ferraz, V. E. D. F., & Brito, L. A. (2014) · Molecular Genetics & Genomic Medicine · doi:10.1002/mgg3.95 · Cited by 83

Royal dynasties as human inbreeding laboratories: the Habsburgs

Ceballos, F. C., & Ortiz-Álvarez, G. (2013) · Heredity · doi:10.1038/hdy.2013.25 · Cited by 79

Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome

Halim, D., Brosens, E., MULLER, F. M., Wangler, M. F., Beaudet, A. L., Lupski, J. R., Coban‐Akdemir, Z., Doukas, M., Stoop, H., de Graaf, B. M., et al. (2017) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2017.05.011 · Cited by 81

Genetic and reproductive consequences of consanguineous marriage in Bangladesh

Anwar, S., Mourosi, J. T., Arafat, S. M. Y., & Hosen, M. J. (2020) · PLoS ONE · doi:10.1371/journal.pone.0241610 · Cited by 86

THE PREVALENCE OF CONSANGUINEOUS MARRIAGES AND AFFECTING FACTORS IN TURKEY: A NATIONAL SURVEY

Kaplan, S., Pınar, G., Kaplan, B., Özçoban, F. A., Karabulut, E., Ayar, B., & Dilmen, U. (2016) · Journal of Biosocial Science · doi:10.1017/s0021932016000055 · Cited by 75

Next-generation community genetics for low- and middle-income countries

Kingsmore, S. F., Lantos, J. D., Dinwiddie, D. L., Miller, N., Soden, S. E., Farrow, E., & Saunders, C. (2012) · Genome Medicine · doi:10.1186/gm324 · Cited by 75

Primary immunodeficiencies in highly consanguineous North African populations

Barbouche, M., Galal, N. M., Ben‐Mustapha, I., Jeddane, L., Mellouli, F., Ailal, F., Béjaoui, M., Boutros, J., Elmarsafy, A. M., & Bousfiha, A. A. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.06260.x · Cited by 72

Ethics in genetic counselling

Clarke, A., & Wallgren-Pettersson, C. (2018) · Journal of Community Genetics · doi:10.1007/s12687-018-0371-7 · Cited by 68

Consanguinity: A blessing or menace at population level?

Bhinder, M. A., Sadia, H., Mahmood, N., Qasim, M., Hussain, Z., Rashid, M., Zahoor, M. Y., Bhatti, R. A., Shehzad, W., Waryah, A. M., et al. (2019) · Annals of Human Genetics · doi:10.1111/ahg.12308 · Cited by 68

Consanguinity and genetic disorders in Egypt

Temtamy, S. A., & Aglan, M. (2012) · Middle East Journal of Medical Genetics · doi:10.1097/01.mxe.0000407744.14663.d8 · Cited by 67

Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency

Ansar, M., Ranza, E., Shetty, M., Paracha, S. A., Azam, M., Kern, I., Iwaszkiewicz, J., Farooq, O. K., Pournaras, C. J., Malclès, A., et al. (2019) · Human Molecular Genetics · doi:10.1093/hmg/ddz303 · Cited by 64

Long-term exposure to ambient air pollution and autism spectrum disorder in children: A case-control study in Tehran, Iran

Yousefian, F., Mahvi, A. H., Yunesian, M., Hassanvand, M. S., Kashani, H., & Amini, H. (2018) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2018.06.259 · Cited by 63

THE CHANGING PROFILE OF CONSANGUINITY RATES IN BAHRAIN, 1990–2009

Arrayed, S. A., & Hamamy, H. (2011) · Journal of Biosocial Science · doi:10.1017/s0021932011000666 · Cited by 58

Consanguineous Marriage, Reproductive Behaviour and Postnatal Mortality in Contemporary Iran

Hosseini‐Chavoshi, M., Abbasi‐Shavazi, M. J., & Bittles, A. H. (2014) · Human Heredity · doi:10.1159/000358403 · Cited by 57

Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages

Vahidnezhad, H., Youssefian, L., Zeinali, S., Saeidian, A. H., Sotoudeh, S., Mozafari, N., Abiri, M., Kajbafzadeh, A. M., Barzegar, M., Ertel, A., et al. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.10.023 · Cited by 56

Prevalence and determinants of consanguineous marriage and its types in India: evidence from the National Family Health Survey, 2015–2016

Sharma, S. K., Kalam, M. A., Ghosh, S., & Roy, S. (2020) · Journal of Biosocial Science · doi:10.1017/s0021932020000383 · Cited by 55

Psychological Distress during Pregnancy in a Multi-Ethnic Community: Findings from the Born in Bradford Cohort Study

Prady, S. L., Pickett, K. E., Croudace, T. J., Fairley, L., Bloor, K. E., Gilbody, S. M., KIERNAN, K. E., & Wright, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060693 · Cited by 55

Skeletal Anomalies in The Neandertal Family of El Sidrón (Spain) Support A Role of Inbreeding in Neandertal Extinction

Ríos, L., Kivell, T. L., Lalueza‐Fox, C., Estalrrich, A., García‐Tabernero, A., Huguet, R., Quintino, Y., de la Rasilla, M., & Rosas, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-38571-1 · Cited by 56

University Students’ knowledge, attitudes, and practices towards the National Premarital Screening Program of Saudi Arabia

Melaibari, M., Shilbayeh, S. A. R., & Kabli, A. (2017) · Journal of the Egyptian Public Health Association · doi:10.21608/epx.2017.7008 · Cited by 52

Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing

Lal, D., Neubauer, B. A., Toliat, M. R., Altmüller, J., Thiele, H., Nürnberg, P., Kamrath, C., Schänzer, A., Sander, T., Hahn, A., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146040 · Cited by 52

Epidemiology of Thalassemia in Gulf Cooperation Council Countries: A Systematic Review

Abu-Shaheen, A. K., Heena, H., Nofal, A., Abdelmoety, D., Al-Matary, A., Alsheef, M. A., & AlFayyad, I. (2020) · BioMed Research International · doi:10.1155/2020/1509501 · Cited by 54

Prevalance of BRCA1 and BRCA2 mutations in familial breast cancer patients in Lebanon

Jalkh, N., Nassar-Slaba, J., Chouery, E., Salem, N., Uhrchammer, N., Golmard, L., Stoppa-Lyonnet, D., Bignon, Y., & Mégarbané, A. (2012) · Hereditary Cancer in Clinical Practice · doi:10.1186/1897-4287-10-7 · Cited by 53

Genetics of Obesity in Consanguineous Populations: Toward Precision Medicine and the Discovery of Novel Obesity Genes

Saeed, S., Arslan, M., & Froguel, P. (2018) · Obesity · doi:10.1002/oby.22064 · Cited by 54

Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short stature

Ansar, M., Ebstein, F., Özkoç, H., Paracha, S. A., Iwaszkiewicz, J., Gesemann, M., Zoete, V., Ranza, E., Santoni, F. A., Sarwar, M. T., et al. (2020) · Human Molecular Genetics · doi:10.1093/hmg/ddaa032 · Cited by 44

Potential social, economic and general health benefits of consanguineous marriage: results from the Born in Bradford cohort study

Bhopal, R. S., Petherick, E., Wright, J., & Small, N. (2013) · European Journal of Public Health · doi:10.1093/eurpub/ckt166 · Cited by 47

Consanguinity and Primary Immunodeficiencies

Al–Herz, W., Al‐Dhekri, H., Barbouche, M., & Rezaei, N. (2014) · Human Heredity · doi:10.1159/000357710 · Cited by 47

Importance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene Functions

Erzurumluoglu, A. M., Shihab, H. A., Rodrı́guez, S., Gaunt, T. R., & Day, I. N. M. (2016) · Annals of Human Genetics · doi:10.1111/ahg.12150 · Cited by 49

Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families

Li, L., Chen, Y., Jiao, X., Jin, C., Jiang, D., Tanwar, M., Ma, Z., Huang, L., Ma, X., Sun, W., et al. (2017) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.17-21424 · Cited by 46

Consanguineous marriage and reproductive risk: attitudes and understanding of ethnic groups practising consanguinity in Western society

Teeuw, M. E., Loukili, G., Bartels, E. A. C., ten Kate, L. P., Cornel, M. C., & Henneman, L. (2013) · European Journal of Human Genetics · doi:10.1038/ejhg.2013.167 · Cited by 44

Classification, clinical features, and genetics of neural tube defects.

Salih, M. A. M., Murshid, W. R., & Seidahmed, M. Z. (2014) · PubMed Central · Cited by 42

RYR2, PTDSS1 and AREG genes are implicated in a Lebanese population-based study of copy number variation in autism

Soueid, J., Kourtian, S., Makhoul, N. J., Makoukji, J., El-Haddad, S., Ghanem, S. S., Kobeissy, F. H., & Boustany, R. (2016) · Scientific Reports · doi:10.1038/srep19088 · Cited by 44

ESTIMATING THE HEALTH AND SOCIOECONOMIC EFFECTS OF COUSIN MARRIAGE IN SOUTH ASIA

Mobarak, A. M., Chaudhry, T. T., Brown, J. S., Zelenska, T., Khan, M. N., Chaudry, S., Wajid, R. A., Bittles, A. H., & Li, S. (2018) · Journal of Biosocial Science · doi:10.1017/s0021932018000275 · Cited by 41

Consanguinity and Prevalence Patterns of Inherited Disease in the UK Pakistani Community

Corry, P. C. (2014) · Human Heredity · doi:10.1159/000362598 · Cited by 40

Thalassemia in the United Arab Emirates: Why it can be prevented but not eradicated

Kim, S., & Tridane, A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0170485 · Cited by 40

The impact of consanguinity on the frequency of inborn errors of metabolism

Afzal, M. U., Lund, A. M., & Skovby, F. (2018) · Molecular Genetics and Metabolism Reports · doi:10.1016/j.ymgmr.2017.11.004 · Cited by 39

Consanguineous marriage in Oman: understanding the community awareness about congenital effects of and attitude towards consanguineous marriage

Islam, M. M. (2016) · Annals of Human Biology · doi:10.1080/03014460.2016.1224385 · Cited by 38

Consanguinity in the Contemporary World

Romeo, G., & Bittles, A. H. (2014) · Human Heredity · doi:10.1159/000363352 · Cited by 38

Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies

Lipov, A., Jurgens, S. J., Mazzarotto, F., Allouba, M., Pirruccello, J. P., Aguib, Y., Gennarelli, M., Yacoub, M. H., Ellinor, P. T., Bezzina, C. R., et al. (2023) · Nature Cardiovascular Research · doi:10.1038/s44161-023-00346-3 · Cited by 38

Effect of consanguinity on birth defects in Saudi women: Results from a nested case‐control study

Majeed‐Saidan, M. A., Ammari, A. N., Alhashem, A. M., Rakaf, M. S. A., Shoukri, M. M., Garne, E., & Kurdi, A. M. (2014) · Birth Defects Research Part A Clinical and Molecular Teratology · doi:10.1002/bdra.23331 · Cited by 40

Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia

Melhem, M., Abu‐Farha, M., Antony, D., Madhoun, A. S. A., Bacchelli, C., Alkayal, F., Al‐Khairi, I., John, S. E., Alomari, M., Beales, P., et al. (2016) · European Journal Of Haematology · doi:10.1111/ejh.12819 · Cited by 37

Identifying Genes Responsible for Intellectual Disability in Consanguineous Families

Iqbal, Z., & van Bokhoven, H. (2014) · Human Heredity · doi:10.1159/000360539 · Cited by 39

The Determinants of Consanguineous Marriages among the Arab Population: A Systematic Review

Goundali, K. E., Chebabe, M., Laamırı, F. Z., & Hilali, A. (2022) · Iranian Journal of Public Health · doi:10.18502/ijph.v51i2.8679 · Cited by 35

Consanguinity, Endogamy and Inborn Errors of Metabolism in Oman: A Cross-Sectional Study

Al‐Thihli, K., Al-Murshedi, F. M., Alhashmi, N., Al-Mamari, W. S., Islam, M. M., & Al‐Yahyaee, S. (2014) · Human Heredity · doi:10.1159/000362686 · Cited by 34

Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of Consanguinity

Youssefian, L., Saeidian, A. H., Palizban, F., Bagherieh, A., Abdollahimajd, F., Sotoudeh, S., Mozafari, N., Farahani, R. A., Mahmoudi, H., Babashah, S., et al. (2021) · Clinical Chemistry · doi:10.1093/clinchem/hvab042 · Cited by 33

Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray

Fan, Y., Ouyang, X., Peng, J., Sacharow, S., Tekin, M., Barbouth, D., Bodamer, O. A., Yusupov, R., Navarrete, C., Heller, A. H., et al. (2013) · Molecular Cytogenetics · doi:10.1186/1755-8166-6-38 · Cited by 35

Consanguinity and epilepsy in Oran, Algeria: A case–control study

Chentouf, A., Talhi, R., Dahdouh, A., Benbihi, L., Benilha, S., Oubaiche, M. L., & Chaouch, M. (2015) · Epilepsy Research · doi:10.1016/j.eplepsyres.2014.12.014 · Cited by 33

Differential impact of consanguineous marriages on autosomal recessive diseases in T unisia

Halim, N. B., Hsouna, S., Lasram, K., Rejeb, I., Walha, A., Talmoudi, F., Messai, H., Brick, A. S. B., Ouragini, H., Cherif, W., et al. (2015) · American Journal of Human Biology · doi:10.1002/ajhb.22764 · Cited by 33

Adolescents in Arab countries: Health statistics and social context

Obermeyer, C. M. (2015) · Doha International Family Institute Journal · doi:10.5339/difi.2015.1 · Cited by 30

Birth defects: Risk factors and consequences

Fett‐Conte, A. C., & Oliveira, C. I. F. (2015) · Journal of Pediatric Genetics · doi:10.3233/pge-13052 · Cited by 31

Success of Face Analysis Technology in Rare Genetic Diseases Diagnosed by Whole-Exome Sequencing: A Single-Center Experience

Elmas, M., & Göğüş, B. (2020) · Molecular Syndromology · doi:10.1159/000505800 · Cited by 29

Consanguineous marriages and congenital anomalies

Bittles, A. H. (2013) · The Lancet · doi:10.1016/s0140-6736(13)61503-2 · Cited by 29

“I am Your Mother and Your Father!” In Vitro Derived Gametes and the Ethics of Solo Reproduction

Cutas, D., & Smajdor, A. (2016) · Health Care Analysis · doi:10.1007/s10728-016-0321-7 · Cited by 27

Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis

Foreman, P. K., Margulis, A. V., Alexander, K., Shediac, R., Calingaert, B., Harding, A., Pladevall, M., & Landis, S. (2021) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-021-01874-6 · Cited by 27

Bartter Syndrome: A Systematic Review of Case Reports and Case Series

Qasba, R. K., Bucharles, A. C. F., Piccoli, M. V. F., Sharma, P., Banga, A., Kamaraj, B., Nawaz, F. A., Kumar, H. J., Happy, M. A., Qasba, R. K., et al. (2023) · Medicina · doi:10.3390/medicina59091638 · Cited by 27

Consanguinity and pregnancy outcomes in a multi-ethnic, metropolitan European population

Becker, R., Keller, T., Wegner, R., Neitzel, H., Stümm, M., Knoll, U., Stärk, M., Fangerau, H., & Bittles, A. H. (2014) · Prenatal Diagnosis · doi:10.1002/pd.4487 · Cited by 27

Modelling the constraints on consanguineous marriage when fertility declines

Barakat, B. F., & Gietel‐Basten, S. (2014) · Demographic Research · doi:10.4054/demres.2014.30.9 · Cited by 27

Attitude of Saudi Arabian adults towards consanguineous marriage

Alharbi, O. A., Al-Shaia, W. A., Al-Hamam, A. A., Al-Marzoug, H. M., Ahmed, A. E., & Bagha, M. (2015) · Qatar medical journal · doi:10.5339/qmj.2015.12 · Cited by 27

ENDOGAMY, CONSANGUINITY AND THE HEALTH IMPLICATIONS OF CHANGING MARITAL CHOICES IN THE UK PAKISTANI COMMUNITY

Small, N., Bittles, A. H., Petherick, E., & Wright, J. (2016) · Journal of Biosocial Science · doi:10.1017/s0021932016000419 · Cited by 27

Under-Five Child Mortality and Morbidity Associated with Consanguineous Child Marriage in Pakistan: Retrospective Analysis using Pakistan Demographic and Health Surveys, 1990–91, 2006–07, 2012–13

Mustafa, M., Zakar, R., Zakar, M. Z., Chaudhry, A., & Nasrullah, M. (2017) · Maternal and Child Health Journal · doi:10.1007/s10995-016-2208-5 · Cited by 27

The Prevention of Thalassemia Revisited: A Historical and Ethical Perspective by the Thalassemia International Federation

Angastiniotis, M., Petrou, M., Loukopoulos, D., Modell, B., Farmakis, D. T., Englezos, P., & Eleftheriou, A. (2021) · Hemoglobin · doi:10.1080/03630269.2021.1872612 · Cited by 26

Prevalence and risk factors of molar incisor hypomineralization in the Middle East: A systematic review and meta-analysis

Bukhari, S. T., Alhasan, H. A., Qari, M. T., Sabbagh, H. J., & Farsi, N. (2022) · Journal of Taibah University Medical Sciences · doi:10.1016/j.jtumed.2022.12.011 · Cited by 26

Consanguinity and Autism

Roy, N., Ghaziuddin, M., & Mohiuddin, S. S. (2020) · Current Psychiatry Reports · doi:10.1007/s11920-019-1124-y · Cited by 26

Specific Aspects of Consanguinity: Some Examples from the Tunisian Population

Romdhane, L., Halim, N. B., Rejeb, I., Kéfi, R., Bouyacoub, Y., Rekaya, M. B., Messai, H., Messaoud, O., Riahi, Z., Bonnet, C., et al. (2014) · Human Heredity · doi:10.1159/000362167 · Cited by 25

Awareness and Attitude Towards the Premarital Screening Programme Among High School Students in Muscat, Oman

Kindi, R. M. A., N/A, Kannekanti, S., N/A, Natarajan, J., N/A, Shakman, L., Alazri, Z., & Al-Kalbani, N. I. (2019) · Sultan Qaboos University medical journal · doi:10.18295/squmj.2019.19.03.007 · Cited by 25

Frequency and management of medically actionable incidental findings from genome and exome sequencing data: a systematic review

Elfatih, A., Mohammed, I., Abdelrahman, D., & Mifsud, B. (2021) · Physiological Genomics · doi:10.1152/physiolgenomics.00025.2021 · Cited by 25

PGAP3 ‐related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation

Abdel‐Hamid, M. S., Issa, M. Y., Otaify, G. A., Abdel‐Ghafar, S. F., Elbendary, H. M., & Zaki, M. S. (2017) · Clinical Genetics · doi:10.1111/cge.13033 · Cited by 25

Band-like calcification with simplified gyration and polymicrogyria: report of 10 new families and identification of five novel OCLN mutations

Abdel‐Hamid, M. S., Abdel‐Salam, G. M. H., Issa, M. Y., Emam, B. A., & Zaki, M. S. (2017) · Journal of Human Genetics · doi:10.1038/jhg.2017.4 · Cited by 25

The illnesses of Charles Darwin and his children: a lesson in consanguinity

Hayman, J., Álvarez, G., Ceballos, F. C., & Berra, T. M. (2017) · Biological Journal of the Linnean Society · doi:10.1093/biolinnean/blw041 · Cited by 24

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

Youssefian, L., Vahidnezhad, H., Saeidian, A. H., Sotoudeh, S., Mahmoudi, H., Daneshpazhooh, M., Aghazadeh, N., Adams, R., Ghanadan, A., Zeinali, S., et al. (2017) · European Journal of Human Genetics · doi:10.1038/ejhg.2017.137 · Cited by 24

Enhancing inclusion of diverse populations in genomics: A competence framework

Sharif, S. M., Blyth, M., Ahmed, M., Sheridan, E. G., Saltus, R., Yu, J., Tonkin, E. T., & Kirk, M. (2020) · Journal of Genetic Counseling · doi:10.1002/jgc4.1263 · Cited by 25

PREVALENCE OF CONSANGUINEOUS MARRIAGES IN SOUTH SINAI, EGYPT

Yamamah, G., Raouf, E. R. A., Talaat, A. A., Saad‐Hussein, A., Hamamy, H. A., & Meguid, N. A. (2012) · Journal of Biosocial Science · doi:10.1017/s002193201200020x · Cited by 24

A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman

Palombo, F., Al-Wardy, N., Gnecchi‐Ruscone, G. A., Oppo, M., Al‐Kindi, M. N., Angius, A., Lamki, K. A., Girotto, G., Giangregorio, T., Benelli, M., et al. (2016) · Journal of Human Genetics · doi:10.1038/jhg.2016.120 · Cited by 24

Beyond the panel: preconception screening in consanguineous couples using the TruSight One “clinical exome”

Kirk, E. P., Barlow-Stewart, K. K., Selvanathan, A., Josephi‐Taylor, S., Worgan, L. C., Rajagopalan, S., Cowley, M. J., Gayevskiy, V., Bittles, A. H., Burnett, L., et al. (2018) · Genetics in Medicine · doi:10.1038/s41436-018-0082-9 · Cited by 23

Association of cerebral palsy with consanguineous parents and other risk factors in a Palestinian population

Daher, S., & El-Khairy, L. (2014) · Eastern Mediterranean Health Journal · doi:10.26719/2014.20.7.459 · Cited by 23

Consanguinity and associated perinatal outcomes, including stillbirth

Kapurubandara, S., Melov, S. J., Shalou, E. R., & Alahakoon, I. (2016) · Australian and New Zealand Journal of Obstetrics and Gynaecology · doi:10.1111/ajo.12493 · Cited by 21

Familial Recurrence of 3MC Syndrome in Consanguineous Families: A Clinical and Molecular Diagnostic Approach with review of the Literature

Gardner, O. K., Haynes, K., Schweitzer, D. N., Johns, A. L., Magee, W. P., Urata, M. M., & Sanchez-Lara, P. A. (2016) · The Cleft Palate-Craniofacial Journal · doi:10.1597/15-151 · Cited by 23

Children at Risk of Specific Learning Disorder: A Study on Prevalence and Risk Factors

Bozatlı, L., Aykutlu, H. C., Giray, A. S., Ataş, T., Özkan, Ç., Yıldırım, B. G., & Görker, I. (2024) · Children · doi:10.3390/children11070759 · Cited by 34

ASSESSMENT OF KNOWLEDGE, ATTITUDE AND PRACTICE TOWARDS CONSANGUINEOUS MARRIAGES AMONG A COHORT OF MULTIETHNIC HEALTH CARE PROVIDERS IN SAUDI ARABIA

Alnaqeb, D., Hamamy, H., Youssef, A. M., & Al-Rubeaan, K. A. (2016) · Journal of Biosocial Science · doi:10.1017/s0021932016000675 · Cited by 22

Variability in laboratory reporting practices for regions of homozygosity indicating parental relatedness as identified by SNP microarray testing

Grote, L. E., Myers, M. F., Lovell, A., Saal, H. M., & Sund, K. L. (2012) · Genetics in Medicine · doi:10.1038/gim.2012.83 · Cited by 21

Effects of diabetes education program on metabolic control among Saudi type 2 diabetic patients

Alshahrani, A. M., Hassan, A., Al-Rubeaan, K. A., Sharqawi, A. H. A., & Ahmad, N. A. (2012) · Cited by 21

Neurological features and outcomes of Wilson’s disease: a single-center experience

Samancı, B., Şahin, E., Bılgıç, B., Tüfekçıoğlu, Z., Gurvit, H. I., Emre, M., Demır, K., & Hanagasi, H. A. (2021) · Neurological Sciences · doi:10.1007/s10072-020-05013-0 · Cited by 20

Exploring the Genetic Landscape of Retinal Diseases in North-Western Pakistan Reveals a High Degree of Autozygosity and a Prevalent Founder Mutation in ABCA4

Rehman, A. U., Peter, V. G., Quinodoz, M., Rashid, A., Khan, S. A., Superti‐Furga, A., & Rivolta, C. (2019) · Genes · doi:10.3390/genes11010012 · Cited by 20

Two new families with enamel renal syndrome: A novel FAM20A gene mutation and review of literature

Hassib, N. F., Shoeib, M., ElSadek, H. A., Wali, M. E., Mostafa, M. I., & Abdel‐Hamid, M. S. (2020) · European Journal of Medical Genetics · doi:10.1016/j.ejmg.2020.104045 · Cited by 19

The Effect of Consanguinity on Neonatal Outcomes and Health

Abbas, H. A., & Yunis, K. A. (2014) · Human Heredity · doi:10.1159/000362125 · Cited by 19

Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree

Makrythanasis, P., Guipponi, M., Santoni, F. A., Zaki, M. S., Issa, M. Y., Ansar, M., Hamamy, H., & Antonarakis, S. E. (2016) · Human Genomics · doi:10.1186/s40246-016-0082-2 · Cited by 19

UK Pakistani views on the adverse health risks associated with consanguineous marriages

Ajaz, M., Ali, N., & Randhawa, G. (2015) · Journal of Community Genetics · doi:10.1007/s12687-015-0214-8 · Cited by 19

Consanguinity and Genomics

(2014) · KARGER eBooks · doi:10.1159/isbn.978-3-318-02703-7 · Cited by 1

Consanguinity: implications for practice, research, and policy

Teebi, A. S., & El‐Shanti, H. (2006) · The Lancet · doi:10.1016/s0140-6736(06)68406-7 · Cited by 41

Consanguineous marriage as socio-medical problem

Bobdjonova, O. B., & Абдурахманова, Ф. М. (2020) · I P Pavlov Russian Medical Biological Herald · doi:10.23888/pavlovj2020282249-258 · Cited by 2

Genetics of consanguineous marriage: Impact and importance of counseling

Akrami, S. M. (2015) · Journal of Pediatric Genetics · doi:10.3233/pge-12034 · Cited by 6

Empirical estimates of the global prevalence of consanguineous marriage in contemporary societies

Bittles, A. H. (1998) · Cited by 38