Mahmoud Aarabi

886 total citations · 1 hit paper
20 papers, 541 citations indexed

About

Mahmoud Aarabi is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mahmoud Aarabi has authored 20 papers receiving a total of 541 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 10 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mahmoud Aarabi's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (5 papers) and Prenatal Screening and Diagnostics (5 papers). Mahmoud Aarabi is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (5 papers) and Prenatal Screening and Diagnostics (5 papers). Mahmoud Aarabi collaborates with scholars based in United States, Canada and Iran. Mahmoud Aarabi's co-authors include Aleksandar Rajkovic, Anthony R. Gregg, Tamar Goldwaser, Emily Chen, Natalia T. Leach, Honey V. Reddi, Teresa N. Sparks, Michael T. Bashford, Susan Klugman and J.S. Dungan and has published in prestigious journals such as SHILAP Revista de lepidopterología, Environmental Health Perspectives and The American Journal of Human Genetics.

In The Last Decade

Mahmoud Aarabi

17 papers receiving 532 citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)

2021 221 citations Anthony R. Gregg, Mahmoud Aarabi et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Mahmoud Aarabi United States	11	214	207	196	103	68	20	541
Julie Richer Canada	13	89 0.4×	399 1.9×	202 1.0×	80 0.8×	103 1.5×	34	670
Jodi D. Hoffman United States	18	119 0.6×	365 1.8×	215 1.1×	74 0.7×	48 0.7×	33	654
Amanda Fortier Canada	8	353 1.6×	200 1.0×	370 1.9×	37 0.4×	160 2.4×	10	678
Gabriel A. Lazarin United States	13	409 1.9×	367 1.8×	98 0.5×	473 4.6×	52 0.8×	27	884
Natalia T. Leach United States	9	245 1.1×	264 1.3×	199 1.0×	113 1.1×	32 0.5×	17	587
Kristina G. Flores United States	15	88 0.4×	264 1.3×	306 1.6×	59 0.6×	67 1.0×	21	794
Vickie Hannig United States	12	83 0.4×	185 0.9×	175 0.9×	103 1.0×	36 0.5×	19	494
Charles M. Strom United States	16	132 0.6×	357 1.7×	241 1.2×	315 3.1×	44 0.6×	37	883
Daniela Bettio Italy	12	235 1.1×	277 1.3×	169 0.9×	20 0.2×	90 1.3×	35	535
Özgül M. Alper Türkiye	13	60 0.3×	134 0.6×	160 0.8×	118 1.1×	25 0.4×	35	472

Countries citing papers authored by Mahmoud Aarabi

Since Specialization

Citations

This map shows the geographic impact of Mahmoud Aarabi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mahmoud Aarabi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mahmoud Aarabi more than expected).

Fields of papers citing papers by Mahmoud Aarabi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mahmoud Aarabi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mahmoud Aarabi. The network helps show where Mahmoud Aarabi may publish in the future.

Co-authorship network of co-authors of Mahmoud Aarabi

This figure shows the co-authorship network connecting the top 25 collaborators of Mahmoud Aarabi. A scholar is included among the top collaborators of Mahmoud Aarabi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mahmoud Aarabi. Mahmoud Aarabi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Wang, John, J.S. Dungan, Anthony R. Gregg, et al.. (2024). Leveraging diverse genomic data to guide equitable carrier screening: Insights from gnomAD v.4.1.0. The American Journal of Human Genetics. 112(1). 181–195. 3 indexed citations

Aarabi, Mahmoud, et al.. (2024). Copy-number variants in the ACMG secondary finding genes: A reporting framework for clinical cytogeneticists. Genetics in Medicine Open. 2. 101839–101839.

Madan‐Khetarpal, Suneeta, et al.. (2024). Recurrent Xp22.31‐Yq11 Unbalanced Translocations: Molecular Diagnosis and Clinical Implications in Three Families. American Journal of Medical Genetics Part A. 197(3). e63913–e63913. 1 indexed citations

Alkhunaizi, Ebba, Mahmoud Aarabi, Selma F. Witchel, et al.. (2023). 45,X/46,XY mosaicism: Clinical manifestations and long term follow‐up. American Journal of Medical Genetics Part A. 194(3). e63451–e63451. 4 indexed citations

Matalon, Dena R., Cinthya Zepeda‐Mendoza, Mahmoud Aarabi, et al.. (2023). Clinical, technical, and environmental biases influencing equitable access to clinical genetics/genomics testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 25(6). 100812–100812. 20 indexed citations

Gregg, Anthony R., Mahmoud Aarabi, Susan Klugman, et al.. (2022). Screening for Autosomal Recessive and X-Linked Conditions During Pregnancy and Preconception: A Practice Resource of the American College of Medical Genetics and Genomics (ACMG). Obstetrical & Gynecological Survey. 77(4). 193–196. 2 indexed citations

Aarabi, Mahmoud, et al.. (2022). A Novel Integrated Approach for Cytogenomic Evaluation of Plasma Cell Neoplasms. Journal of Molecular Diagnostics. 24(10). 1067–1078.

Aarabi, Mahmoud, Jacqueline Baumann, Melanie Babcock, et al.. (2022). Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots. Psychiatric Genetics. 32(5). 171–177.

Aarabi, Mahmoud, et al.. (2022). Carrier frequency of autosomal recessive genetic conditions in diverse populations: Lessons learned from the genome aggregation database. Clinical Genetics. 102(2). 87–97. 11 indexed citations

10.

Gregg, Anthony R., Mahmoud Aarabi, Susan Klugman, et al.. (2021). Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 23(10). 1793–1806. 221 indexed citations breakdown →

11.

Lambrot, Romain, Donovan Chan, Xiaojian Shao, et al.. (2021). Whole-genome sequencing of H3K4me3 and DNA methylation in human sperm reveals regions of overlap linked to fertility and development. Cell Reports. 36(3). 109418–109418. 28 indexed citations

12.

Yatsenko, Svetlana A., Mahmoud Aarabi, Jie Hu, et al.. (2020). Copy number alterations involving 59 ACMG ‐recommended secondary findings genes. Clinical Genetics. 98(6). 577–588. 3 indexed citations

13.

Chan, Donovan, Xiaojian Shao, Marie-Charlotte Dumargne, et al.. (2019). Customized MethylC-Capture Sequencing to Evaluate Variation in the Human Sperm DNA Methylome Representative of Altered Folate Metabolism. Environmental Health Perspectives. 127(8). 87002–87002. 20 indexed citations

14.

Aarabi, Mahmoud, E Kessler, Suneeta Madan‐Khetarpal, et al.. (2018). Autism spectrum disorder in females with ARHGEF9 alterations and a random pattern of X chromosome inactivation. European Journal of Medical Genetics. 62(4). 239–242. 12 indexed citations

15.

Aarabi, Mahmoud, et al.. (2018). Chromosomal instability in women with primary ovarian insufficiency. Human Reproduction. 33(3). 531–538. 24 indexed citations

16.

Aarabi, Mahmoud, Huaiyang Jiang, Devereux N. Saller, et al.. (2018). Importance of complete phenotyping in prenatal whole exome sequencing. Human Genetics. 137(2). 175–181. 54 indexed citations

17.

Ly, Lundi, Donovan Chan, Mahmoud Aarabi, et al.. (2017). Intergenerational impact of paternal lifetime exposures to both folic acid deficiency and supplementation on reproductive outcomes and imprinted gene methylation. Molecular Human Reproduction. 23(7). 461–477. 85 indexed citations

18.

Aarabi, Mahmoud, Kioomars Saliminejad, Mohammad Reza Sadeghi, et al.. (2009). Deletion and Testicular Expression of DAZ (Deleted in Azoospermia) Gene in Patients with Non-Obstructive Azoospermia. SHILAP Revista de lepidopterología. 1 indexed citations

19.

Aarabi, Mahmoud, et al.. (2008). Association of TGIFLX/Y mRNA expression with azoospermia in infertile men. Molecular Reproduction and Development. 75(12). 1761–1766. 13 indexed citations

20.

Mobasheri, Maryam Beigom, et al.. (2007). Expression of two testis-specific genes, TSGA10 and SYCP3, in different cancers regarding to their pathological features. Cancer Detection and Prevention. 31(4). 296–302. 39 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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