Publications by authors named "Behar D"

West and South Asian populations profoundly influenced Eurasian genetic and cultural diversity. We investigate the genetic history of the Y chromosome haplogroup L1-M22, which, while prevalent in these regions, lacks in-depth study. Robust Bayesian analyses of 165 high-coverage Y chromosomes favor a West Asian origin for L1-M22 ∼20.

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  • The study evaluated the effectiveness of a targeted Israeli expanded carrier screening panel (IL-ECSP) designed for the diverse Israeli population, beyond standard testing provided by health authorities.* -
  • Over an 18-month period, 10,115 samples were analyzed, revealing that 25% of couples had no concerning findings, while 24.3% had both partners as carriers of different genetic conditions, identifying numerous couples at risk.* -
  • The findings suggest that nearly half of the at-risk couples would not have been detected using standard screenings, highlighting the importance of expanding the targeted screening panel to enhance reproductive decision-making.*
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Aims: The objective of this work is to evaluate the epidemiological profile of colorectal cancers, histologically proven over a 5-year period (2012-2016) in the Tlemcen region.

Methods: A retrospective study of 581 cases of colorectal cancer collected at the epidemiology department of the University Hospital Center (UHC) of Tlemcen between January 2012 and December 2016 was performed. Epidemiological data were processed using SPSS version 25 and Microsoft Excel 2010.

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Parity non-conservation (PNC) due to the weak interaction is predicted to give rise to enantiomer dependent vibrational constants in chiral molecules, but the phenomenon has so far eluded experimental observation. The enhanced sensitivity of molecules to physics beyond the Standard Model (BSM) has led to substantial advances in molecular precision spectroscopy, and these may be applied to PNC searches as well. Specifically, trapped molecular ion experiments leverage the universality of trapping charged particles to optimize the molecular ion species studied toward BSM searches, but in searches for PNC, only a few chiral molecular ion candidates have been proposed so far.

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Ludwig van Beethoven (1770-1827) remains among the most influential and popular classical music composers. Health problems significantly impacted his career as a composer and pianist, including progressive hearing loss, recurring gastrointestinal complaints, and liver disease. In 1802, Beethoven requested that following his death, his disease be described and made public.

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Sea level rise (SLR) is a long-lasting consequence of climate change because global anthropogenic warming takes centuries to millennia to equilibrate for the deep ocean and ice sheets. SLR projections based on climate models support policy analysis, risk assessment and adaptation planning today, despite their large uncertainties. The central range of the SLR distribution is estimated by process-based models.

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Including sea-level rise (SLR) projections in planning and implementing coastal adaptation is crucial. Here we analyze the first global survey on the use of SLR projections for 2050 and 2100. Two-hundred and fifty-three coastal practitioners engaged in adaptation/planning from 49 countries provided complete answers to the survey which was distributed in nine languages - Arabic, Chinese, English, French, Hebrew, Japanese, Korean, Portuguese and Spanish.

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  • Recessive dystrophic epidermolysis bullosa (RDEB) is a rare skin condition stemming from mutations in the COL7A1 gene responsible for type VII collagen.
  • This study analyzed 32 patient samples from various regions in the Americas to trace the origins of COL7A1 mutations and their impact on disease prevalence.
  • Findings indicate that RDEB mutations have both European and American roots, with some linked to Sephardic ancestry, highlighting the importance of understanding genetic backgrounds for future treatment developments.
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  • Scientists studied the rare types of Y-chromosomes (which help tell about a person's male ancestry) in northern and eastern Europe to learn more about the history of these regions.
  • They used a lot of detailed DNA sequences to find new groups of these rare Y-chromosomes and figured out when they started appearing.
  • Their findings showed that some of these Y-chromosome groups came from recent increases in the population, while others showed links to ancient peoples from Siberia.
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Human Y chromosome haplogroup J1-M267 is a common male lineage in West Asia. One high-frequency region-encompassing the Arabian Peninsula, southern Mesopotamia, and the southern Levant-resides ~ 2000 km away from the other one found in the Caucasus. The region between them, although has a lower frequency, nevertheless demonstrates high genetic diversity.

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Next generation sequencing tests are used routinely as first-choice tests in the clinic. However, systematic performance comparing the results of exome sequencing as a single test replacing Sanger sequencing of targeted gene(s) is still lacking. Performance comparison data are critically important for clinical case management.

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The phylogenetic analysis of Y chromosomal haplogroup O2a-M95 was crucial to determine the nested structure of South Asian branches within the larger tree, predominantly present in East and Southeast Asia. However, it had previously been unclear that how many founders brought the haplogroup O2a-M95 to South Asia. On the basis of the updated Y chromosomal tree for haplogroup O2a-M95, we analysed 1437 male samples from South Asia for various novel downstream markers, carefully selected from the extant phylogenetic tree.

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Background: We assessed in a nationwide cohort the association between adolescent BMI and early-onset (< 40 years) type 2 diabetes among Israelis of Ethiopian origin.

Methods: Normoglycemic adolescents (range 16-20 years old), including 93,806 native Israelis (≥ 3rd generation in Israel) and 27,684 Israelis of Ethiopian origin, were medically assessed for military service between 1996 and 2011. Weight and height were measured.

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Purpose: Stomach cancer is a major global health problem; it is one of the ten most common cancers with poor survival, and its incidence is characterized by wide variation. The aim of this work is to carry out a retrospective epidemiological study on gastric cancer in the wilaya of Tlemcen (West Algeria) over a period of 5 years (2011-2015).

Methods: The data set was provided by the cancer registry of the Tlemcen wilaya.

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  • Researchers conducted genome sequencing on the skeletal remains of Hungarian King Béla III and eight others to trace the origins of the Árpád Dynasty.
  • Y-chromosome analysis showed that Béla III and one other individual belonged to haplogroups indicating a connection to South Central Asia, particularly modern Iran and the Caucasus.
  • The closest living relatives of the Árpád Dynasty are identified as the modern Bashkirs from Bashkortostan, with their ancestry tracing back to Northern Afghanistan approximately 4500 years ago.
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Purpose: Increased implementation of complex genetic technologies in clinical practice emphasizes the urgency of genomic literacy and proficiency for medical professionals. We evaluated our genomic education model.

Methods: We assessed the 5-day, extended format program, encompassing lectures, videos, interactive tests, practice cases, and clinical exercises.

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Marine litter is one of the most pressing problems of our time and a major threat to ocean health; much of it comes from land-based sources, including from beachgoer activities. This study investigates how product design could influence littering behaviors of beachgoers when applied to beach trash cans (TCs). Over the course of six weeks three differently designed TCs were placed on a Mediterranean Sea tourist beach in Israel while observers tracked the behavior of 536 nearby groups ("entities") of beachgoers.

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Purpose: Mutations in the gene HSD17B3 encoding the 17-beta hydroxysteroid dehydrogenase 3 enzyme cause testosterone insufficiency leading to XY disorders of sex development. In this study the clinical and molecular characteristics of three patients from consanguineous families are elucidated.

Methods: We identified three patients from two unrelated families with XY DSD and a novel homozygous HSD17B3:c.

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The presence of genomic signatures of Eurasian origin in contemporary Ethiopians has been reported by several authors and estimated to have arrived in the area from 3000 years ago. Several studies reported plausible source populations for such a signature, using haplotype based methods on modern data or single-site methods on modern or ancient data. These studies did not reach a consensus and suggested an Anatolian or Sardinia-like proxy, broadly Levantine or Neolithic Levantine as possible sources.

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Immigration from one cultural milieu to another has been associated with a greater risk for incident cardio-metabolic morbidity among adults. In this nationwide, population-based, cross-sectional study of data recorded from 1992 to 2016, we assessed the association between body mass index and blood pressure levels among adolescent immigrants, aged 16 to 19 years, of Ethiopian origin, and their secular trend of overweight and obesity. Adolescents of Ethiopian origin were classified as Israeli-born (n=16 153) or immigrants (N=23 487), with stratification by age at immigration.

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Purpose: Expanded preconception carrier screening (ECS) identifies at-risk couples (ARCs) for multiple diseases. ECS reports currently include only pathogenic/likely pathogenic variants (P/LPVs). Variants of unknown significance (VUS) are not reported, unlike genomic or chromosomal array test results in other post/prenatal settings.

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  • The mutational spectrum of BRCA1 and BRCA2 genes in the Middle East, North Africa, and Southern Europe is not well understood due to unique cultural practices like consanguinity that may lead to specific genetic variants.
  • A comprehensive search of scientific databases and collaboration with local researchers uncovered 232 pathogenic sequence variants (PSVs) in BRCA1 and 239 in BRCA2 across 25 of 33 surveyed countries.
  • Some mutations were found to repeat across multiple countries, indicating that targeted genotyping of these common variants could serve as an effective first step in BRCA testing for these populations.*
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Much marine litter comes from land-based sources, with a significant amount coming from activities on bathing beaches. Thus, the overall focus of this exploratory research is to identify elements important for the design of beach infrastructure (i.e.

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