Shareef Nahas

3.9k citations

43 papers · 1.8k indexed · 1 hit paper · h-index 22

Molecular Biology top 10%
Genetics top 5%
Cancer Research top 5%
Hematology top 2%
Oncology top 10%

Co-authors: Richard A. Gatti Liutao Du Chih‐Hung Lai Stephen F. Kingsmore David Dimmock Shimul Chowdhury Helen H. Chun Nathaly M. Sweeney
Topics: DNA Repair Mechanisms (23 papers)Carcinogens and Genotoxicity Assessment (11 papers)Genomics and Rare Diseases (6 papers)
Cited by: Hematology Cancer Research Genetics
Journals: Cell Proceedings of the National Academy of Sciences The Journal of Experimental Medicine
Partner nations: United States Netherlands Germany

In The Last Decade

Shareef Nahas

43 papers receiving 1.8k citations

Hit Papers

align trajectories

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.

Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization

2018 280 citations Lauge Farnaes, Amber Hildreth et al. npj Genomic Medicine profile →

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-authorship network of co-authors of Shareef Nahas

This figure shows the co-authorship network connecting the top 25 collaborators of Shareef Nahas. A scholar is included among the top collaborators of Shareef Nahas 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 Shareef Nahas. Shareef Nahas 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

#	Work	Indexed citations
1	Identification of SARS-CoV-2 variants using viral sequencing for the Centers for Disease Control and Prevention genomic surveillance program 2022 ·BMC Infectious Diseases ·Chirayu Goswami,Michael Sheldon,(unknown),Mehdi Keddache,(unknown),Yihe Wang,(unknown),(unknown),(unknown),Elaine Kwon,Steven Buyske,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Shareef Nahas	23
2	Developmental and temporal characteristics of clonal sperm mosaicism 2021 ·Cell ·Xiaoxu Yang,Martin W. Breuss,(unknown),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,(unknown),Yan Ding,Jonathan Sebat,Joseph G. Gleeson	26
3	Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers 2019 ·Molecular Genetics & Genomic Medicine ·Job A.J. Verdonschot,Emma Robinson,Kiely N. James,(unknown),Godelieve R.F. Claes,Kari Casas,Els K. Vanhoutte,Mark R. Hazebroek,(unknown),(unknown),Arthur van den Wijngaard,Jan F. C. Glatz,Stéphane Heymans,Ingrid P.C. Krapels,Shareef Nahas,Han G. Brunner,Radek Szklarczyk	12
4	Biallelic loss of GNAS in a patient with pediatric medulloblastoma 2019 ·Molecular Case Studies ·Mari Tokita,Shareef Nahas,Benjamin Briggs,Denise Malicki,Jill P. Mesirov,Iris Reyes,Lauge Farnaes,Michael L. Levy,Stephen F. Kingsmore,David Dimmock,John R. Crawford,Robert J. Wechsler‐Reya	6
5	Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalizationbreakdown → 2018 ·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	280
6	Rapid whole-genome sequencing identifies a novel AIRE variant associated with autoimmune polyendocrine syndrome type 1 2018 ·Molecular Case Studies ·Erica Sanford Kobayashi,Kelly Watkins,Shareef Nahas,Michael Gottschalk,Nicole G. Coufal,Lauge Farnaes,David Dimmock,Stephen F. Kingsmore,(unknown)	5
7	Rapid whole-genome sequencing identifies a novel homozygous NPC1 variant associated with Niemann–Pick type C1 disease in a 7-week-old male with cholestasis 2017 ·Molecular Case Studies ·Amber Hildreth,Kristen Wigby,Shimul Chowdhury,Shareef Nahas,Jaime Barea,(unknown),Serge Batalov,David Dimmock,Stephen F. Kingsmore,(unknown)	9
8	Assaying Radiosensitivity of Ataxia-Telangiectasia 2017 ·Methods in molecular biology ·Hailiang Hu,Shareef Nahas,Richard A. Gatti	7
9	Rapid whole-genome sequencing identifies a novel GABRA1 variant associated with West syndrome 2017 ·Molecular Case Studies ·Lauge Farnaes,Shareef Nahas,Shimul Chowdhury,J.G. Nelson,Serge Batalov,David Dimmock,Stephen F. Kingsmore,(unknown)	16
10	Impact of TP53 mutation variant allele frequency on phenotype and outcomes in myelodysplastic syndromes 2015 ·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	137
11	ATM–Dependent MiR-335 Targets CtIP and Modulates the DNA Damage Response 2013 ·PLoS Genetics ·Nathan Martin,Kotoka Nakamura,(unknown),Shareef Nahas,(unknown),(unknown),Richard A. Gatti,Hailiang Hu	44
12	A New Series of Small Molecular Weight Compounds Induce Read Through of All Three Types of Nonsense Mutations in the ATM Gene 2013 ·Molecular Therapy ·Liutao Du,Michael E. Jung,Robert Damoiseaux,Gladys C. Completo,Francesca Fike,Jin‐Mo Ku,Shareef Nahas,(unknown),Hailiang Hu,Richard A. Gatti	44
13	Common copy number variations in fifty radiosensitive cell lines 2011 ·Genomics ·Xinmin Li,Jian Zhou,Shareef Nahas,(unknown),Hailiang Hu,Richard A. Gatti	6
14	Defective DNA double‐strand break repair in pediatric systemic lupus erythematosus 2011 ·Arthritis & Rheumatism ·(unknown),(unknown),Francesca Fike,Jiexi Wang,Shareef Nahas,(unknown),Hailiang Hu,Richard A. Gatti,Deborah McCurdy	33
15	Functional and computational assessment of missense variants in the ataxia-telangiectasia mutated (ATM) gene: mutations with increased cancer risk 2008 ·Human Mutation ·Midori Mitui,Shareef Nahas,Liutao Du,(unknown),Chih‐Hung Lai,Kotoka Nakamura,(unknown),(unknown),(unknown),Patrick Concannon,Martin F. Lavin,Richard A. Gatti	53
16	Transcriptional response to ionizing radiation in human radiation sensitive cell lines 2007 ·Radiotherapy and Oncology ·(unknown),Shareef Nahas,Jørgen Aarøe,Richard A. Gatti,(unknown),Olaug K. Rødningen	5
17	ATM Gene Founder Haplotypes and Associated Mutations in Polish Families with Ataxia‐Telangiectasia 2005 ·Annals of Human Genetics ·Midori Mitui,Ewa Bernatowska,Barbara Pietrucha,Janina Piotrowska‐Jastrzębska,(unknown),Shareef Nahas,Sharon N. Teraoka,(unknown),(unknown),Patrick Concannon,Richard A. Gatti	33
18	Inhibition of Atm and/or Atr disrupts gene silencing on the inactive X chromosome 2005 ·Biochemical and Biophysical Research Communications ·Yan Ouyang,Jennifer L. Salstrom,(unknown),Shareef Nahas,(unknown),David W. Dawson,Michael A. Teitell,Steve Horvath,Arthur D. Riggs,Richard A. Gatti,York Marahrens	13
19	Improved diagnostic testing for ataxia–telangiectasia by immunoblotting of nuclear lysates for ATM protein expression 2003 ·Molecular Genetics and Metabolism ·Helen H. Chun,Xia Sun,Shareef Nahas,Sharon N. Teraoka,Chih‐Hung Lai,Patrick Concannon,Richard A. Gatti	64
20	Five haplotypes account for fifty‐five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: Seven new mutations 2003 ·American Journal of Medical Genetics Part A ·(unknown),Midori Mitui,Catarina D. Campbell,Beatriz Tavares Costa‐Carvalho,Shareef Nahas,Xia Sun,(unknown),(unknown),Yvonne R. Thorstenson,(unknown),Salmo Raskin,Chong Ae Kim,Juan Clinton Llerena,Richard A. Gatti	23

About Shareef Nahas

Shareef Nahas is a scholar working on Cancer Research, Molecular Biology and Genetics, having authored 43 papers that have together received 1.8k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (23 papers), Carcinogens and Genotoxicity Assessment (11 papers) and Genomics and Rare Diseases (6 papers). The work is most often cited by research in Hematology (360 citations), Cancer Research (403 citations) and Genetics (570 citations). Shareef Nahas has collaborated with scholars based in United States, Netherlands and Germany. Frequent co-authors include Richard A. Gatti, Liutao Du, Chih‐Hung Lai, Stephen F. Kingsmore, David Dimmock, Shimul Chowdhury, Helen H. Chun, Nathaly M. Sweeney, Hailiang Hu and Midori Mitui. Their work appears in journals such as Cell, Proceedings of the National Academy of Sciences and The Journal of Experimental Medicine.

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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