Nader Chalhoub

2.9k total citations · 1 hit paper
18 papers, 1.5k citations indexed

About

Nader Chalhoub is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Nader Chalhoub has authored 18 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Genetics. Recurrent topics in Nader Chalhoub's work include Hereditary Neurological Disorders (4 papers), PI3K/AKT/mTOR signaling in cancer (4 papers) and Bone Metabolism and Diseases (4 papers). Nader Chalhoub is often cited by papers focused on Hereditary Neurological Disorders (4 papers), PI3K/AKT/mTOR signaling in cancer (4 papers) and Bone Metabolism and Diseases (4 papers). Nader Chalhoub collaborates with scholars based in United States, Qatar and Canada. Nader Chalhoub's co-authors include Suzanne J. Baker, Jean Vacher, Nadia Benachenhou, Venkatesh Rajapurohitam, Annalisa Frattini, Anna Villa, Monica Pata, Mathieu Ferron, Xiaoyan Zhu and Guo Zhu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Genes & Development.

In The Last Decade

Nader Chalhoub

18 papers receiving 1.5k 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.

PTEN and the PI3-Kinase Pathway in Cancer

2008 965 citations Nader Chalhoub, Suzanne J. Baker Annual Review of Pathology Mechanisms of Disease profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nader Chalhoub United States	11	1.2k	347	287	167	145	18	1.5k
Lydia W.T. Cheung Hong Kong	20	987 0.8×	348 1.0×	332 1.2×	116 0.7×	109 0.8×	40	1.6k
Josema Torres Spain	17	1.7k 1.4×	318 0.9×	225 0.8×	173 1.0×	198 1.4×	25	2.0k
Jianfei Xue China	15	1.3k 1.1×	320 0.9×	418 1.5×	198 1.2×	89 0.6×	22	1.7k
Landon J. Inge United States	21	1.1k 0.9×	433 1.2×	307 1.1×	128 0.8×	153 1.1×	41	1.7k
Andrew Chantry United Kingdom	24	1.4k 1.1×	415 1.2×	326 1.1×	178 1.1×	56 0.4×	43	1.9k
Carmela Ciccarelli Italy	20	941 0.8×	245 0.7×	383 1.3×	120 0.7×	91 0.6×	29	1.4k
Bruce D. Cuevas United States	19	1.5k 1.2×	430 1.2×	308 1.1×	271 1.6×	109 0.8×	25	2.1k
Daniel L. Altschuler United States	22	1.0k 0.8×	294 0.8×	115 0.4×	145 0.9×	91 0.6×	35	1.6k
Xiaohua Xin United States	16	1.2k 1.0×	292 0.8×	373 1.3×	82 0.5×	98 0.7×	34	1.8k
Sharmistha Chakraborty United States	23	891 0.7×	303 0.9×	211 0.7×	112 0.7×	209 1.4×	41	1.4k

Countries citing papers authored by Nader Chalhoub

Since Specialization

Citations

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

Fields of papers citing papers by Nader Chalhoub

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nader Chalhoub

This figure shows the co-authorship network connecting the top 25 collaborators of Nader Chalhoub. A scholar is included among the top collaborators of Nader Chalhoub 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 Nader Chalhoub. Nader Chalhoub is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

Chalhoub, Nader, et al.. (2023). Myosteatosis and Frailty Factors associated with the occurrence of Complications in Cirrhotic patients: MYOFACC study. 7(1). 19–27. 1 indexed citations

Aguiar‐Pulido, Vanessa, Alexander Martinez‐Fundichely, Eran Elhaik, et al.. (2021). Systems biology analysis of human genomes points to key pathways conferring spina bifida risk. Proceedings of the National Academy of Sciences. 118(51). 10 indexed citations

Aleem, Alice Abdel, Mahmoud F. Elsaid, Nader Chalhoub, et al.. (2020). Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant. Neuromuscular Disorders. 30(6). 457–471. 15 indexed citations

Elsaid, Mahmoud F., et al.. (2017). NT5C2 novel splicing variant expands the phenotypic spectrum of Spastic Paraplegia (SPG45): case report of a new member of thin corpus callosum SPG-Subgroup. BMC Medical Genetics. 18(1). 33–33. 14 indexed citations

Elsaid, Mahmoud F., Nader Chalhoub, Tawfeg Ben‐Omran, et al.. (2017). Homozygous nonsense mutation in SCHIP1/IQCJ‐SCHIP1 causes a neurodevelopmental brain malformation syndrome. Clinical Genetics. 93(2). 387–391. 2 indexed citations

Elsaid, Mahmoud F., Nader Chalhoub, Tawfeg Ben‐Omran, et al.. (2016). Mutation in noncoding RNA RNU12 causes early onset cerebellar ataxia. Annals of Neurology. 81(1). 68–78. 57 indexed citations

Elsaid, Mahmoud F., Nader Chalhoub, M S Ehlayel, et al.. (2015). Non‐truncating LIFR mutation: causal for prominent congenital pain insensitivity phenotype with progressive vertebral destruction?. Clinical Genetics. 89(2). 210–216. 11 indexed citations

Kumar, Pankaj, Mashael Al‐Shafai, Nader Chalhoub, et al.. (2014). Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance. BMC Research Notes. 7(1). 747–747. 10 indexed citations

Chalhoub, Nader, Guo Zhu, Xiaoyan Zhu, & Suzanne J. Baker. (2009). Cell type specificity of PI3K signaling in Pdk1- and Pten-deficient brains. Genes & Development. 23(14). 1619–1624. 59 indexed citations

10.

Frappart, Pierre‐Olivier, Youngsoo Lee, H. R. Russell, et al.. (2009). Recurrent genomic alterations characterize medulloblastoma arising from DNA double-strand break repair deficiency. Proceedings of the National Academy of Sciences. 106(6). 1880–1885. 65 indexed citations

11.

Chalhoub, Nader & Suzanne J. Baker. (2008). PTEN and the PI3-Kinase Pathway in Cancer. Annual Review of Pathology Mechanisms of Disease. 4(1). 127–150. 965 indexed citations breakdown →

12.

Chalhoub, Nader, Sara C. Kozma, & Suzanne J. Baker. (2006). S6k1 is not required for Pten-deficient neuronal hypertrophy. Brain Research. 1100(1). 32–41. 19 indexed citations

13.

Quarello, Paola, Marco Forni, Laura Barberis, et al.. (2004). Severe Malignant Osteopetrosis Caused by a GL Gene Mutation. Journal of Bone and Mineral Research. 19(7). 1194–1199. 42 indexed citations

14.

Chalhoub, Nader, Nadia Benachenhou, Venkatesh Rajapurohitam, et al.. (2003). Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human. Nature Medicine. 9(4). 399–406. 199 indexed citations

15.

Li, Wentian, et al.. (2002). Linkage disequilibrium and founder effect analysis of the NF1 gene in French Canadians from the Quebec population. Annales de Génétique. 45(1). 39–44. 2 indexed citations

16.

Rajapurohitam, Venkatesh, Nader Chalhoub, Nadia Benachenhou, et al.. (2001). The mouse osteopetrotic grey-lethal mutation induces a defect in osteoclast maturation/function. Bone. 28(5). 513–523. 48 indexed citations

17.

Chalhoub, Nader, Nadia Benachenhou, & Jean Vacher. (2001). Physical and transcriptional map of the mouse Chromosome 10 proximal region syntenic to human 6q16-q21. Mammalian Genome. 12(12). 887–892. 9 indexed citations

18.

Fang, Lijuan, Nader Chalhoub, Wentian Li, et al.. (2001). Genotype analysis of theNF1 gene in the French Canadians from the Qu�bec population. American Journal of Medical Genetics. 104(3). 189–198. 4 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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