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

Bittles, A. H., Mason, W. M., Greene, J., & Rao, N. A. (1991) · Science · doi:10.1126/science.2028254 · Cited by 331

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

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

History of the methodology of disease gene identification

Antonarakis, S. E. (2021) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.62400 · Cited by 18

Genetic Insights from Consanguineous Cardiomyopathy Families

Maurer, C., Boleti, O., Torbati, P. N., Norouzi, F., Fowler, A. N. R., Minaee, S., Salih, K. H., Taherpour, M., Birjandi, H., Alizadeh, B., et al. (2023) · Genes · doi:10.3390/genes14010182 · Cited by 18

Consanguinity as a Risk Factor for Autism

Alshaban, F. A. W., Aldosari, M., Ghazal, I., Al‐Shammari, H., Elhag, S. F., Thompson, I. R., Bruder, J., Shaath, H., Al‐Faraj, F., Tolefat, M., et al. (2023) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-023-06137-w · Cited by 18

Family Health History

Bennett, R. L. (2019) · Medical Clinics of North America · doi:10.1016/j.mcna.2019.06.002 · Cited by 21

Prenatal and preconception genetic counseling for consanguinity: Consanguineous couples' expectations, experiences, and perspectives

Thain, E., Shuman, C. T., Miller, K., Sappleton, K., Myles‐Reid, D., Chitayat, D. A., & Gibbons, C. (2019) · Journal of Genetic Counseling · doi:10.1002/jgc4.1150 · Cited by 17

Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families

Zhou, Y., Tariq, M., He, S., Abdullah, U., Zhang, J., & Baig, S. M. (2020) · BMC Medical Genetics · doi:10.1186/s12881-020-01087-x · Cited by 17

The Sociodemographic and Economic Correlates of Consanguineous Marriages in Highly Consanguineous Populations

Hamamy, H., & Alwan, S. S. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-420195-8.00018-5 · Cited by 17

Has the long-predicted decline in consanguineous marriage in India occurred?

Kumari, N., Bittles, A. H., & Saxena, P. C. (2019) · Journal of Biosocial Science · doi:10.1017/s0021932019000762 · Cited by 17

Genome-wide inbreeding estimation within Lebanese communities using SNP arrays

Jalkh, N., Sahbatou, M., Chouery, É., Mégarbané, A., Leutenegger, A., & Serre, J. (2014) · European Journal of Human Genetics · doi:10.1038/ejhg.2014.246 · Cited by 16

Consanguineous marriage and its relevance to divorce, polygyny and survival of marriage: evidence from a population-based analysis in Jordan

Islam, M. M. (2021) · Annals of Human Biology · doi:10.1080/03014460.2021.1877354 · Cited by 16

Intensive Kinship, Development, and Demography: Why Pakistan has the Highest Rates of Cousin Marriage in the World

Shenk, M. K., Naz, S., & Chaudhry, T. T. (2024) · Population and Development Review · doi:10.1111/padr.12678 · Cited by 15

Prenatal genetic counseling and consanguinity

Posch, A., Springer, S., Langer, M., Blaicher, W., Streubel, B., & Schmid, M. P. (2012) · Prenatal Diagnosis · doi:10.1002/pd.3971 · Cited by 15

Consanguinity and its association with visual impairment in southern India: the Pavagada Pediatric Eye Disease Study 2

Kemmanu, V., Giliyar, S. K., Rao, H. L., Shetty, B. K., Kumaramanickavel, G., & McCarty, C. A. (2018) · Journal of Community Genetics · doi:10.1007/s12687-018-0401-5 · Cited by 15

Genetic counseling and screening of consanguineous couples and their offspring practice resource: Focused Revision

Bennett, R. L., Malleda, N. R., Byers, P. H., Steiner, R. D., & Barr, K. (2021) · Journal of Genetic Counseling · doi:10.1002/jgc4.1477 · Cited by 14

CATCHing putative causative variants in consanguineous families

Santoni, F. A., Makrythanasis, P., & Antonarakis, S. E. (2015) · BMC Bioinformatics · doi:10.1186/s12859-015-0727-5 · Cited by 14

Risk factors associated with congenital hypothyroidism: a case-control study in southeast Iran

Khammarnia, M., Siakholak, F. R., Ansari, H., & Peyvand, M. (2018) · Electronic physician · doi:10.19082/6286 · Cited by 14

Dental Anomalies in Consanguineous Marriage: A Clinical-Radiological Study

Bağcı, N., Pamukçu, U., Altunkaynak, B., & Peker, İ. (2021) · International Dental Journal · doi:10.1016/j.identj.2021.02.003 · Cited by 14

First steps in exploring prospective exome sequencing of consanguineous couples

Teeuw, M. E., Waisfisz, Q., Zwijnenburg, P. J. G., Sistermans, E. A., Weiss, M. M., Henneman, L., ten Kate, L. P., Cornel, M. C., & Meijers-Heijboer, H. E. J. (2014) · European Journal of Medical Genetics · doi:10.1016/j.ejmg.2014.09.003 · Cited by 14

History’s Masters: The Effect of European Monarchs on State Performance

Ottinger, S., & Voigtländer, N. (2020) · National Bureau of Economic Research · doi:10.3386/w28297 · Cited by 14

Consanguinity and willingness to perform premarital genetic screening in Sudan

Elhadi, Y. A. M., Alrawa, S. S. K., Alfadul, E. S. A., Mahgoub, E. A. A., El-Osta, A. A. R., Belal, S. A., Lucero‐Prisno, D. E., Dabbah, N. A. E., & Yahia, A. (2023) · European Journal of Human Genetics · doi:10.1038/s41431-023-01438-1 · Cited by 13

Oral Phenotype and Salivary Microbiome of Individuals With Papillon–Lefèvre Syndrome

Lettieri, G. M., Santiago, L. M., Lettieri, G. C., Borges, L. G. D. A., Marconatto, L., de Oliveira, L. A., Damé‐Teixeira, N., & Salles, L. P. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.720790 · Cited by 13

Prevalence and Risk Factors of Consanguineous Marriage

Heidari, F., Dastgiri, S., Akbari, R., Khamnian, Z., Khanlarzadeh, E., Binazir, M. B., Jabbary-Fam, S., Badrazar, S., Heidarzadeh, M., & Tajaddini, N. (2014) · Electronic Journal of General Medicine · doi:10.15197/sabad.1.11.81 · Cited by 13

Consanguineous Marriage and its Relationship with Sociocultural Variables in Urban and Bedouin Geographical Regions in Kuwait

Al‐Kandari, Y. Y., & Al‐Kandari, Y. Y. (2018) · Arabian Humanities · doi:10.4000/cy.3731 · Cited by 13

Parental exome analysis identifies shared carrier status for a second recessive disorder in couples with an affected child

Mor‐Shaked, H., Rips, J., Gershon-Naamat, S., Reich, A., Elpeleg, O. N., Meiner, V., & Harel, T. (2020) · European Journal of Human Genetics · doi:10.1038/s41431-020-00756-y · Cited by 13

Consanguinity-based analysis of exome sequencing yields likely genetic causes in patients with inherited retinal dystrophy

Shen, R., Wang, J.-G., Li, Y., & Jin, Z. (2021) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-021-01902-5 · Cited by 13

A comprehensive genetic landscape of inherited retinal diseases in a large Pakistani cohort

Ullah, M., Rehman, A. U., Quinodoz, M., Rashid, A., Cancellieri, F., Munir, A., Kamińska, K., Iqbal, A., Javed, S., Dawood, M., et al. (2025) · npj Genomic Medicine · doi:10.1038/s41525-025-00488-2 · Cited by 12

Change in the Prevalence and Determinants of Consanguineous Marriages in India between National Family and Health Surveys of 1992–1993 and 2015–2016

Kalam, Sharma, Ghosh, & Roy (2020) · Human Biology · doi:10.13110/humanbiology.92.2.02 · Cited by 12

Autosomal dominant hereditary ataxia in Sri Lanka

Sumathipala, D., Abeysekera, G. S., Jayasekara, R. W., Tallaksen, C. M. E., & Dissanayake, V. H. W. (2013) · BMC Neurology · doi:10.1186/1471-2377-13-39 · Cited by 12

Challenges in the care for consanguineous couples: an exploratory interview study among general practitioners and midwives

Teeuw, M. E., Hagelaar, A., ten Kate, L. P., Cornel, M. C., & Henneman, L. (2012) · BMC Family Practice · doi:10.1186/1471-2296-13-105 · Cited by 12

Opportunity for Selection in Human Health

Govindaraju, D. R. (2014) · Advances in genetics · doi:10.1016/b978-0-12-800149-3.00001-9 · Cited by 11

Infant deaths from congenital anomalies: novel use of Child Death Overview Panel data

Firth, C., Petherick, E., & Oddie, S. (2018) · Archives of Disease in Childhood · doi:10.1136/archdischild-2017-314256 · Cited by 11

A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report

Manoochehri, J., Dastgheib, S. A., Khamirani, H. J., Mollaie, M., Sharifi, Z., Zoghi, S., Tabei, K., Mohammadi, S., Dehghanian, F., Farbood, Z., et al. (2021) · Human Genome Variation · doi:10.1038/s41439-021-00164-8 · Cited by 11

Consanguinity in the Chaouia population (Morocco): prevalence, trends, determinants, fertility, and spontaneous abortions

Cheffi, K., Dahbi, N., Khair, A. E., Stambouli, H., Elbouri, A., Talbi, J., Hilali, A., & Ossmani, H. E. (2022) · Egyptian Journal of Medical Human Genetics · doi:10.1186/s43042-022-00337-2 · Cited by 11

Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders

Saadi, S. M., Calì, E., Khalid, L. B., Yousaf, H., Zafar, G., Khan, H. N., Sher, M., Vona, B., Abdullah, U., Malik, N. A., et al. (2023) · Genes · doi:10.3390/genes14071404 · Cited by 11

Principles of Human Genetics and Mendelian Inheritance

Germain, D. P., & Simina, I.-E. (2018) · Springer eBooks · doi:10.1007/978-3-319-76148-0_1 · Cited by 11

Congenital Hypotonia: Cracking a SAGA of consanguineous kindred harboring four genetic variants

Kalfon, L., Baydany, M., Samra, N. N., Heno, N., Segal, Z. I., Eran, A., Yulevich, A., Fellig, Y., Mandel, H., & Zaccai, T. C. F. (2021) · Molecular Genetics & Genomic Medicine · doi:10.1002/mgg3.1849 · Cited by 11

An ESHG–ESHRE survey on the current practice of expanded carrier screening in medically assisted reproduction

Capalbo, A., de Wert, G. M. W. R., Henneman, L., Kakourou, G., Mcheik, S., Peterlin, B., van El, C. G., Vassena, R., Vermeulen, N., Viville, S., et al. (2024) · Human Reproduction · doi:10.1093/humrep/deae131 · Cited by 10

Consanguinity and Occurrence of Monogenic Diseases in a Single Tertiary Centre in Riyadh, Saudi Arabia: A 2 Years Cross-Sectional Study

Alshamlani, L. K., Alsulaim, D. S., Alabbad, R. S., Alhoshan, A. A., Alkhoder, J. F., Alsaleh, N. S., Almannai, M., Ababneh, F., Algattan, M., Alsini, L., et al. (2024) · The Application of Clinical Genetics · doi:10.2147/tacg.s476350 · Cited by 10

Genome Sequencing Identifies 13 Novel Candidate Risk Genes for Autism Spectrum Disorder in a Qatari Cohort

Ben‐Mahmoud, A., Gupta, V. R., Aleem, A. K. A., Thompson, I. R., Aden, A., Mbarek, H., Saad, C., Tolefat, M., Alshaban, F. A. W., Stanton, L. W., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252111551 · Cited by 14

Accelerated MEN2A in homozygous RET carriers in the context of consanguinity

Machens, A., & Dralle, H. (2024) · European Journal of Endocrinology · doi:10.1093/ejendo/lvae025 · Cited by 10

High-Throughput Sequencing and Rare Genetic Diseases

Makrythanasis, P., & Antonarakis, S. E. (2012) · Molecular Syndromology · doi:10.1159/000343941 · Cited by 10

Triple A syndrome with a novel indel mutation in the AAAS gene and delayed puberty

Bustanji, H., Sahar, B., Huebner, A., Ajlouni, K. M., Landgraf, D., Hamamy, H., & Koehler, K. (2015) · Journal of Pediatric Endocrinology and Metabolism · doi:10.1515/jpem-2014-0401 · Cited by 10

Community engagement and education: addressing the needs of South Asian families with genetic disorders

Khan, N., Kerr, G., & Kingston, H. M. (2016) · Journal of Community Genetics · doi:10.1007/s12687-016-0278-0 · Cited by 10

User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia

Josephi‐Taylor, S., Barlow-Stewart, K. K., Selvanathan, A., Roscioli, T., Bittles, A. H., Meiser, B., Worgan, L. C., Rajagopalan, S., Colley, A., & Kirk, E. P. (2018) · Journal of Genetic Counseling · doi:10.1007/s10897-018-0298-5 · Cited by 10

Paternal Factors Associated with Neonatal Deaths and Births with Low Weight: Evidence from Pakistan Demographic and Health Survey 2006–2007

Zakar, R., Zakar, M. Z., Aqil, N., & Nasrullah, M. (2015) · Maternal and Child Health Journal · doi:10.1007/s10995-015-1674-5 · Cited by 10

Promoting international, locally focused, and patient-oriented genetic counseling

Weil, J., Alaeddin, D. S., Awwad, R. I., Chanouha, N., Elbassiouny, B., Furqan, A., Jacobs, M. F., Kavanaugh, G., Neogi, A., Rao, S. K., et al. (2024) · Genetics in Medicine Open · doi:10.1016/j.gimo.2024.101880 · Cited by 9

A Multidisciplinary Perspective Addressing the Diagnostic Challenges of Late-Onset Pompe Disease in the Arabian Peninsula Region Developed From an Expert Group Meeting

Shehri, A. A., Al-Asmi, A. R., Salti, A. M. A., Almadani, A., Hassan, A., Bamaga, A. K., Cupler, E., Al-Hashel, J., Alabdali, M. M., Alanazy, M. H., et al. (2022) · Journal of Neuromuscular Diseases · doi:10.3233/jnd-220819 · Cited by 9

Comprehension of premarital screening and genetic disorders among the population of Riyadh

AlOtaiby, S., Alqahtani, A., Saleh, R., Mazyad, A., Albohigan, A., & Kutbi, E. (2023) · Journal of Taibah University Medical Sciences · doi:10.1016/j.jtumed.2023.01.006 · Cited by 9

Family aggregation of language impairment in an isolated Chilean population from Robinson Crusoe Island

Barbieri, Z. D., Fernández, M. A., Newbury, D. F., & Villanueva, P. (2018) · International Journal of Language & Communication Disorders · doi:10.1111/1460-6984.12377 · Cited by 11

The Development of Human Genetics at the National Research Centre, Cairo, Egypt: A Story of 50 Years

Temtamy, S. A. (2019) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-083118-015201 · Cited by 9

Association between consanguineous marriage and child nutritional outcomes among currently married women in Pakistan

Chauhan, B. G., Yadav, D., & Jungari, S. B. (2019) · Clinical Epidemiology and Global Health · doi:10.1016/j.cegh.2019.04.003 · Cited by 9

Consanguinity rates among Syrian refugees in Lebanon: a study on genetic awareness

Sabeh, M. E., Kassir, M. F., Ghanem, P., Saifi, O., Hadi, D. E., Khalifeh, Y., Akkawi, A. R., Ghabach, M. M., Chaaya, M., Nemer, G. M., et al. (2020) · Journal of Biosocial Science · doi:10.1017/s002193202000022x · Cited by 9

Outcome of pregnancies with first‐trimester increased nuchal translucency and cystic hygroma in a tertiary maternity hospital in United Arab Emirates

Narava, S., Singh, S. B., Barpanda, S., & Bricker, L. (2022) · International Journal of Gynecology & Obstetrics · doi:10.1002/ijgo.14222 · Cited by 9

Consanguineous Marriage: Protective or Risk Factor for Intimate Partner Violence?

Usta, J., Khawaja, M., Dandachi, D., & Salem, M. T. (2015) · Springer eBooks · doi:10.1007/978-3-319-16670-4_5 · Cited by 9

Variable approaches to genetic counseling for microarray regions of homozygosity associated with parental relatedness

Grote, L. E., Myers, M. F., Lovell, A., Saal, H. M., & Sund, K. L. (2013) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.36206 · Cited by 9

Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder

Polla, D. L., Fard, M. A. F., Tabatabaei, Z., Habibzadeh, P., Levchenko, O. A., Nikuei, P., Makrythanasis, P., Hussain, M., Hardenberg, S. V., Zeinali, S., et al. (2021) · Genetics in Medicine · doi:10.1038/s41436-021-01133-w · Cited by 9

Effects of a Genetic Counseling Model on Mothers of Children with Down Syndrome: A Brazilian Pilot Study

Micheletto, M. R. D., Valério, N. I., & Fett‐Conte, A. C. (2013) · Journal of Genetic Counseling · doi:10.1007/s10897-013-9619-x · Cited by 9

The structure of first-cousin marriages in Brazil

Otto, P. A., Lemes, R. B., de Farias, A. A., Weller, M., Lima, S. O. A., Albino, V. A., Marques-Alves, Y. K., Pardono, E., Bocángel, M. A. P., & Santos, S. (2020) · Scientific Reports · doi:10.1038/s41598-020-72366-z · Cited by 8

Consanguinity in northwest Pakistan: evidence of temporal decline

Malik, S., Bibi, A., Farid, R., Khan, S., Awan, J., & Rehman, A. U. (2024) · Journal of Biosocial Science · doi:10.1017/s0021932024000026 · Cited by 8

Implantable and Wearable Neuroengineering Education: A Review of Postgraduate Programmes

Ghannam, R., Curia, G., Brante, G. G. D. O., Khosravi, S., & Fan, H. (2020) · IEEE Access · doi:10.1109/access.2020.3040064 · Cited by 8

Effectiveness and Adverse Effects of Risperidone in Children with Autism Spectrum Disorder in a Naturalistic Clinical Setting at a University Hospital in Oman

Al‐Huseini, S., Al-Barhoumi, A., Al-Balushi, M., Al-Hosni, A., Al-Mahrouqi, T., Al-Mahrizi, B., Jaju, S., & Mirza, H. (2022) · Autism Research and Treatment · doi:10.1155/2022/2313851 · Cited by 8

Mutual compensation of the effects of religious and ethnic homogamy on reproduction

Huber, S., & Fieder, M. (2017) · American Journal of Human Biology · doi:10.1002/ajhb.23064 · Cited by 8

A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene

Sayeb, M., Riahi, Z., Laroussi, N., Bonnet, C., Romdhane, L., Mkaouar, R., Zaouak, A., Marrakchi, J., Abdessalem, G., Messaoud, O., et al. (2019) · International Journal of Dermatology · doi:10.1111/ijd.14452 · Cited by 8

Education and Consanguineous Marriage

Akyol, Ş. P., & Mocan, N. H. (2020) · National Bureau of Economic Research · doi:10.3386/w28212 · Cited by 8

History's Masters The Effect of European Monarchs on State Performance

Ottinger, S., & Voigtländer, N. (2025) · Econometrica · doi:10.3982/ecta20830 · Cited by 7

Impact of Parental Consanguinity on the Frequency of Orofacial Clefts in Jordan

Jabaiti, S., Salah, B., Al‐lawama, M., AlRyalat, S. A., Jabaiti, O., Al-Mikhi, B., Alsmady, D., & Al-Basti, H. B. (2021) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000008294 · Cited by 7

The utility of exome sequencing in diagnosing pediatric neurodevelopmental disorders in a highly consanguineous population

Khalaf, T., Ojaimi, M. A., Saleh, D. A., Sulaiman, A., Sohal, A. P. S., Khan, A. O., & El‐Hattab, A. W. (2024) · Clinical Genetics · doi:10.1111/cge.14508 · Cited by 7

Assessing Students’ Knowledge and Attitudes Regarding the Risks and Prevention of Consanguineous Marriage: A Cross-Sectional Online Survey

Jairoun, A. A., Al‐Hemyari, S. S., Shahwan, M. J., Karuniawati, H., Zyoud, S. H., Abu‐Gharbieh, E., Zyoud, S. H., Al‐Ani, M., Habeb, M., & Jairoun, M. (2024) · Journal of Multidisciplinary Healthcare · doi:10.2147/jmdh.s449348 · Cited by 7

Genetic Variant Analyses Identify Novel Candidate Autism Risk Genes from a Highly Consanguineous Cohort of 104 Families from Oman

Gupta, V. R., Ben‐Mahmoud, A., Idris, A. B., Hottenga, J., Habbab, W., Alsayegh, A., Kim, H., Al‐Mamari, W., & Stanton, L. W. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413700 · Cited by 10

Social and Demographic Determinants of Consanguineous Marriage: Insights from a Literature Review

Popescu, G., Rusu, C., Maștaleru, A., Oancea, A., Cumpăt, C. M., Luca, M. C., Grosu, C., & Leon, M. M. (2025) · Genealogy · doi:10.3390/genealogy9030069 · Cited by 7

Taurine newborn screening to prevent one form of retinal degeneration and cardiomyopathy

Antonarakis, S. E. (2020) · European Journal of Human Genetics · doi:10.1038/s41431-020-0671-3 · Cited by 7

Unbiased phenotype and genotype matching maximizes gene discovery and diagnostic yield

Rips, J., Halstuk, O., Fuchs, A., Lang, Z., Sido, T., Gershon-Naamat, S., Abu‐Libdeh, B., Edvardson, S., Salah, S., Breuer, O., et al. (2024) · Genetics in Medicine · doi:10.1016/j.gim.2024.101068 · Cited by 7

Infant mortality in Italy: large geographic and ethnic inequalities

Simeoni, S., Frova, L., & Curtis, M. D. (2024) · The Italian Journal of Pediatrics/Italian journal of pediatrics · doi:10.1186/s13052-023-01571-z · Cited by 7

A population-based cross-sectional study on consanguineous marriages in rural Tamil Nadu, India

Saleem, M. T. S., Kanagasabapathy, S., & Sabeetha, K. (2015) · International Journal of Medical Science and Public Health · doi:10.5455/ijmsph.2016.20112015221 · Cited by 7

Chromosome Microarrays in Diagnostic Testing: Interpreting the Genomic Data

Peters, G. B., & Pertile, M. D. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-0847-9_8 · Cited by 7

A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation

Gutierrez‐Rodrigues, F., Masri, N., Chouery, É., Diamond, C. E., Jalkh, N., Vicente, A., Kajigaya, S., Abillama, F. F., Bejjani, N. A., Serhal, W., et al. (2019) · Human Genetics · doi:10.1007/s00439-019-02076-8 · Cited by 7

Consanguinité et son impact sur la santé et la dynamique du génome : Un exemple de la Tunisie

Mezzi, N., Abassi, N., Fatnassi, F., Abdelhak, S., & Romdhane, L. (2024) · La Tunisie Médicale · doi:10.62438/tunismed.v102i5.4787 · Cited by 6

Ancient DNA reveals diverse community organizations in the 5th millennium BCE Carpathian Basin

Szécsényi‐Nagy, A., Virag, C., Jakab, K., Rohland, N., Ringbauer, H., Anders, A., Raczky, P., Hajdu, T., Kiss, K., Szeniczey, T., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60368-2 · Cited by 8

Consanguineous Marriage and Early Pregnancy Loss in Rural to Peri-Urban India

Robertson, J. M., Basany, K., Farooq, F., Tan, X., Tang, G., Bunker, C. H., Reddy, P. S., & Haggerty, C. L. (2021) · The Journal of Obstetrics and Gynecology of India · doi:10.1007/s13224-021-01498-7 · Cited by 6

Experience using singleton exome sequencing of probands as an approach to preconception carrier screening in consanguineous couples

Abulí, A., Costa‐Roger, M., Codina‐Solà, M., Valenzuela, I., Leno-Colorado, J., Rovira‐Moreno, E., Cueto-González, A. M., Fernández‐Álvarez, P., García‐Arumí, E., Cuscó, I., et al. (2022) · Journal of Medical Genetics · doi:10.1136/jmg-2022-108607 · Cited by 6

Parent Awareness and Perceived Barriers Regarding Hearing Impairment among School Age Children in Taif Region of Saudi Arabia

Fageeh, Y. A., Alghoribi, M. H., Albishi, M. M., Alshanbari, A., Alqethami, A. A., Altowairqi, T. M., & Alosaimi, N. K. (2023) · Journal of Pharmacy And Bioallied Sciences · doi:10.4103/jpbs.jpbs_527_22 · Cited by 6

The clinical and socioeconomic aspects of t-cell receptor excision circle based newborn screening for severe combined immunodeficiency in Southeast and East Asia

Yoo, N., Kim, S., Kim, J., Ahn, J. G., Kang, I., & Shin, J. J. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1549768 · Cited by 7

Relationship Between Consanguineous Marriages and Incidence and Severity of Refractive Errors: A Cross-sectional Study

Alsaqr, A. M. (2019) · International Journal of Ophthalmology & Visual Science · doi:10.11648/j.ijovs.20190404.15 · Cited by 6

COVID-19: Impact on linguistic and genetic isolates of India

Singh, P. P., Suravajhala, P., Mallick, C. B., Tamang, R., Kumar, A., Machha, P., Singh, R., Pathak, A., Mishra, V. N., Shrivastava, P., et al. (2021) · Genes and Immunity · doi:10.1038/s41435-021-00150-8 · Cited by 6

Evaluation of hepcidin, ferritin and iron levels with liver enzymes of β-thalassemia patients in Diyala governorate, Iraq

Abd, H. M., & Samarrai, O. R. A. (2022) · AIP conference proceedings · doi:10.1063/5.0096262 · Cited by 6

Characterization of the Consanguinity in the Moroccan Population of Doukkala

Khair, A. E., Dahbi, N., Cheffi, K., Talbi, J., Hilali, A., & Ossmani, H. E. (2023) · Journal of Social Sciences · doi:10.3844/jssp.2023.15.21 · Cited by 6

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

PENYAKIT BAWAAN : KAJIAN RESIKO KESEHATAN PADA PERKAWINAN SEPUPU

Yusdiawati, Y. (2018) · Jurnal Antropologi Isu-Isu Sosial Budaya · doi:10.25077/jaisb.v19.n2.p89-99.2017 · Cited by 6

Single-nucleotide polymorphism arrays and unexpected consanguinity: considerations for clinicians when returning results to families

Delgado, F., Tabor, H. K., Chow, P. M., Conta, J. H., Feldman, K. W., Tsuchiya, K. D., & Beck, A. E. (2014) · Genetics in Medicine · doi:10.1038/gim.2014.119 · Cited by 6

Etiology and diagnosis of cerebral palsy in resource-limited regions

SINGHI, P. D., & Saini, A. G. (2025) · Seminars in Pediatric Neurology · doi:10.1016/j.spen.2025.101226 · Cited by 5

Unpacking the link between cousin marriage and women's paid work

Khalil, S. (2024) · Social Science Research · doi:10.1016/j.ssresearch.2024.103061 · Cited by 5

The elusive associations of nucleotides with human success: evolutionary genetics in education and social policies

Govindaraju, D. R., & Goldstein, A. M. (2025) · Evolution Education and Outreach · doi:10.1186/s12052-025-00218-3 · Cited by 5

Influence of Consanguinity and Medication on the Development of Parkinson’s Disease

Tufail, M., & Hassan, I. (2020) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000509586 · Cited by 5

The cousin marriage tradition and performance of businesses during the economic crises in Nigeria

Estrin, S., Mickiewicz, T. M., & Olarewaju, T. I. A. (2024) · World Development · doi:10.1016/j.worlddev.2024.106910 · Cited by 5

Acute respiratory failure and generalized hypotonia secondary to vitamin D dependent rickets type 1A

Ahmad, N., Sobaihi, M. M., Al-Jabri, M., Al-Esaei, N. A., & Alzaydi, A. M. (2018) · International Journal of Pediatrics and Adolescent Medicine · doi:10.1016/j.ijpam.2018.05.001 · Cited by 5

Nephronophthisis due to a novel DCDC2 variant in a patient from African‐Caribbean descent: A case report

Slater, B. A., Bekheirnia, N., Angelo, J., Bi, W., Braun, M., & Bekheirnia, M. R. (2019) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.61440 · Cited by 5

Female parental consanguinity is associated with a reduced ovarian reserve

Melado, L., Lawrenz, B., Vitorino, R. L., Coughlan, C., Altobelli, G., Bayram, A., Arnanz, A., Elkhatib, I., Munck, N. D., & Fatemi, H. M. (2021) · Reproductive BioMedicine Online · doi:10.1016/j.rbmo.2021.11.023 · Cited by 5

An Exploration of Genetic Test Utilization, Genetic Counseling, and Consanguinity within the Inborn Errors of Metabolism Collaborative (IBEMC)

Stein, Q., Vockley, C. W., Edick, M. J., Zhai, S., Hiner, S. J., Loman, R., Davis‐Keppen, L., Zuck, T., Cameron, C. A., Berry, S. A., et al. (2017) · Journal of Genetic Counseling · doi:10.1007/s10897-017-0100-0 · Cited by 5

High Concordance of Copy Number Variants Detected by Chromosomal Microarray and Exome Sequencing in Clinical Diagnostics

Birnbaum, R., Slovik, M., Zenvirt, S., Livyatan, I., Altman, I., Gershon, S., Rips, J., Daum, H., Rosenbluh, C., Elpeleg, O. N., et al. (2025) · Clinical Genetics · doi:10.1111/cge.70079 · Cited by 4

Incidence of Inborn Errors of Metabolism in Newborn Infants: Five Years’ Single-Center Experience, Jeddah, Saudi Arabia

Qurashi, M., Alahmadi, S., Mustafa, A., Aga, S. S., Hindi, M. A., Ahmed, A., Mohammad, H., ElSharabasy, R., Abed, S. S., AlThubaiti, I., et al. (2023) · Clinical Pediatrics · doi:10.1177/00099228231163511 · Cited by 4

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