Shareef Nahas

4.0k citations

43 papers · 1.9k · 1 hit paper · h-index 22

Impact in

Hematology top 2%
- Acute Myeloid Leukemia Research
Cancer Research top 5%
- Carcinogens and Genotoxicity Assessment
- Cancer Genomics and Diagnostics

Papers in

Molecular Biology 29
- DNA Repair Mechanisms 21
- CRISPR and Genetic Engineering 5
- RNA and protein synthesis mechanisms 4
Genetics 11
- Genomics and Rare Diseases 5
- Genetics and Neurodevelopmental Disorders 3

Co-authors: Richard A. Gatti (23 shared papers)Liutao Du (6 shared papers)David Dimmock (12 shared papers)Chih‐Hung Lai (4 shared papers)Stephen F. Kingsmore (12 shared papers)Shimul Chowdhury (9 shared papers)Helen H. Chun (3 shared papers)Nathaly M. Sweeney (4 shared papers)
Journals: Molecular Case Studies (6 papers)npj Genomic Medicine (3 papers)Neuromuscular Disorders (2 papers)Blood (2 papers)Human Mutation (2 papers)
Partner nations: United States Netherlands Germany

In The Last Decade

Shareef Nahas

43 papers receiving 1.8k citations

Shareef Nahas's Hit Papers

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Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization 2018 · 284 citations

Peers

Countries citing papers authored by Shareef Nahas

Since Specialization

Citations

This map shows the geographic impact of Shareef Nahas'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 Shareef Nahas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shareef Nahas more than expected).

Fields of papers citing papers by Shareef Nahas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shareef Nahas. 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 Shareef Nahas. The network helps show where Shareef Nahas may publish in the future.

Co-authors

The 25 scholars most cited alongside Shareef Nahas, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Shareef Nahas Line = papers co-authored together Shareef Nahas links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

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#	Work
1	Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization npj Genomic Medicine ·Lauge Farnaes, Amber Hildreth, Nathaly M. Sweeney, Michelle M. Clark, Shimul Chowdhury, Shareef Nahas, Julie A. Cakici, Wendy Benson, Robert H. Kaplan, Richard Kronick, Matthew N. Bainbridge, Jennifer Friedman, Jeffrey J. Gold, Yan Ding, Narayanan Veeraraghavan, David Dimmock, Stephen F. Kingsmore Hit paper breakdown →	2018	284
2	MDS-associated somatic mutations and clonal hematopoiesis are common in idiopathic cytopenias of undetermined significance Blood ·Brian Kwok, Jeff Hall, John S. Witte, Yin Xu, Prashanti Reddy, Keming Lin, Rachel Flamholz, Bashar Dabbas, Aine Yung, Jenan Al-Hafidh, Emily Balmert, Christine Vaupel, Carlos Hader, Matthew J. McGinniss, Shareef Nahas, Julie Kines, Rafael Bejar	2015	217
3	Impact of TP53 mutation variant allele frequency on phenotype and outcomes in myelodysplastic syndromes Leukemia ·David A. Sallman, Rami S. Komrokji, Christine Vaupel, Thomas Cluzeau, Susan Geyer, Kathy L. McGraw, Najla H. Al Ali, Jeffrey E. Lancet, Matthew J. McGinniss, Shareef Nahas, Alexander Smith, Austin Kulasekararaj, G J Mufti, Alan F. List, Jeff Hall, Eric Padron	2015	141
4	Correction of ATM gene function by aminoglycoside-induced read-through of premature termination codons Proceedings of the National Academy of Sciences ·Chih‐Hung Lai, Helen H. Chun, Shareef Nahas, Midori Mitui, Kristin M. Gamo, Liutao Du, Richard A. Gatti	2004	128
5	Nonclassical splicing mutations in the coding and noncoding regions of the ATM Gene: Maximum entropy estimates of splice junction strengths Human Mutation ·Laura Eng, Gabriela Coutinho, Shareef Nahas, G Yeo, Robert Tanouye, Mahnoush Babaei, Thilo Dörk, Christopher B. Burge, Richard A. Gatti	2003	125
6	Nonaminoglycoside compounds induce readthrough of nonsense mutations The Journal of Experimental Medicine ·Liutao Du, Robert Damoiseaux, Shareef Nahas, Kun Gao, Hailiang Hu, Julianne M. Pollard, Jimena Goldstine, Michael E. Jung, Susanne M. Henning, Carmen Bertoni, Richard A. Gatti	2009	112
7	Rapid Whole Genome Sequencing Has Clinical Utility in Children in the PICU* Pediatric Critical Care Medicine ·Erica Sanford Kobayashi, Michelle M. Clark, Lauge Farnaes, Matthew R. Williams, James C. Perry, Elizabeth Ingulli, Nathaly M. Sweeney, Ami Doshi, Jeffrey J. Gold, Benjamin Briggs, Matthew N. Bainbridge, Michele Feddock, Kelly Watkins, Shimul Chowdhury, Shareef Nahas, David Dimmock, Stephen F. Kingsmore, Nicole G. Coufal	2019	91
8	Improved diagnostic testing for ataxia–telangiectasia by immunoblotting of nuclear lysates for ATM protein expression Molecular Genetics and Metabolism ·Helen H. Chun, Xia Sun, Shareef Nahas, Sharon N. Teraoka, Chih‐Hung Lai, Patrick Concannon, Richard A. Gatti	2003	65
9	Homozygous deficiency of ubiquitin-ligase ring-finger protein RNF168 mimics the radiosensitivity syndrome of ataxia-telangiectasia Cell Death and Differentiation ·S S Devgan, Özden Sanal, Carsten Doil, Kotoka Nakamura, Shareef Nahas, Kelly Pettijohn, Jiří Bártek, Claudia Lukas, Jiří Lukáš, Richard A. Gatti	2011	63
10	Functional and computational assessment of missense variants in the ataxia-telangiectasia mutated (ATM) gene: mutations with increased cancer risk Human Mutation ·Midori Mitui, Shareef Nahas, Liutao Du, Ziguo Yang, Chih‐Hung Lai, Kotoka Nakamura, S. Arroyo, S. P. Scott, A. Purayidom, Patrick Concannon, Martin F. Lavin, Richard A. Gatti	2008	53
11	Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease npj Genomic Medicine ·Nathaly M. Sweeney, Shareef Nahas, Shimul Chowdhury, Serge Batalov, Michelle M. Clark, Sara Caylor, Julie A. Cakici, John J. Nigro, Yan Ding, Narayanan Veeraraghavan, Charlotte A. Hobbs, David Dimmock, Stephen F. Kingsmore	2021	52
12	ATM–Dependent MiR-335 Targets CtIP and Modulates the DNA Damage Response PLoS Genetics ·Nathan Martin, Kotoka Nakamura, Robert C. Davies, Shareef Nahas, Christina Brown, Rashmi Tunuguntla, Richard A. Gatti, Hailiang Hu	2013	46
13	A New Series of Small Molecular Weight Compounds Induce Read Through of All Three Types of Nonsense Mutations in the ATM Gene Molecular Therapy ·Liutao Du, Michael E. Jung, Robert Damoiseaux, Gladys C. Completo, Francesca Fike, Jin‐Mo Ku, Shareef Nahas, Cijing Piao, Hailiang Hu, Richard A. Gatti	2013	44
14	DNA double strand break repair defects, primary immunodeficiency disorders, and ‘radiosensitivity’ Current Opinion in Allergy and Clinical Immunology ·Shareef Nahas, Richard A. Gatti	2009	40
15	Defective DNA double‐strand break repair in pediatric systemic lupus erythematosus Arthritis & Rheumatism ·Robert C. Davies, Kelly Pettijohn, Francesca Fike, Jiexi Wang, Shareef Nahas, Rashmi Tunuguntla, Hailiang Hu, Richard A. Gatti, Deborah McCurdy	2011	33
16	ATM Gene Founder Haplotypes and Associated Mutations in Polish Families with Ataxia‐Telangiectasia Annals of Human Genetics ·Midori Mitui, Ewa Bernatowska, Barbara Pietrucha, Janina Piotrowska‐Jastrzębska, Laura Eng, Shareef Nahas, Sharon N. Teraoka, Gretchen Louise Sholty, A. Purayidom, Patrick Concannon, Richard A. Gatti	2005	33
17	Assessing ‘radiosensitivity’ with kinetic profiles of γ-H2AX, 53BP1 and BRCA1 foci Radiotherapy and Oncology ·Nathan Martin, Shareef Nahas, Rashmi Tunuguntla, Francesca Fike, Richard A. Gatti	2011	30
18	Rapid Flow Cytometry–Based Structural Maintenance of Chromosomes 1 (SMC1) Phosphorylation Assay for Identification of Ataxia-Telangiectasia Homozygotes and Heterozygotes Clinical Chemistry ·Shareef Nahas, Anthony W. Butch, Liutao Du, Richard A. Gatti	2009	29
19	Developmental and temporal characteristics of clonal sperm mosaicism Cell ·Xiaoxu Yang, Martin W. Breuss, Xin Xu, Danny Antaki, Kiely N. James, Valentina Stanley, Laurel Ball, Renee D. George, Sara A. Wirth, Beibei Cao, An Nguyen, Jennifer McEvoy‐Venneri, Guoliang Chai, Shareef Nahas, Lucitia Van Der Kraan, Yan Ding, Jonathan Sebat, Joseph G. Gleeson	2021	26
20	Five haplotypes account for fifty‐five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: Seven new mutations American Journal of Medical Genetics Part A ·Gabriela Coutinho, Midori Mitui, Catarina D. Campbell, Beatriz Tavares Costa‐Carvalho, Shareef Nahas, Xia Sun, Yong Huo, Chih‐hung Lai, Yvonne R. Thorstenson, Robert Tanouye, Salmo Raskin, Chong Ae Kim, Juan Clinton Llerena, Richard A. Gatti	2003	23

About Shareef Nahas

Shareef Nahas is a scholar working on Molecular Biology, Genetics, Cancer Research, Oncology and Hematology, having authored 43 papers that have together received 1.9k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (21 papers), Carcinogens and Genotoxicity Assessment (6 papers), Cancer Genomics and Diagnostics (5 papers), Cancer-related Molecular Pathways (5 papers), Genomics and Rare Diseases (5 papers), CRISPR and Genetic Engineering (5 papers), RNA and protein synthesis mechanisms (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Hematology (355 citations), Cancer Research (346 citations), Genetics (529 citations), Genetics (183 citations) and Molecular Biology (943 citations). Shareef Nahas has collaborated with scholars based in United States, Netherlands and Germany. Frequent co-authors include Richard A. Gatti, Liutao Du, David Dimmock, Chih‐Hung Lai, Stephen F. Kingsmore, Shimul Chowdhury, Helen H. Chun, Nathaly M. Sweeney, Hailiang Hu and Midori Mitui. Their work appears in journals such as Molecular Case Studies, npj Genomic Medicine, Neuromuscular Disorders, Blood and Human Mutation.

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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Shareef Nahas

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