Elliott H. Sherr

10.7k total citations · 1 hit paper
104 papers, 5.0k citations indexed

About

Elliott H. Sherr is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Elliott H. Sherr has authored 104 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Genetics, 45 papers in Pediatrics, Perinatology and Child Health and 34 papers in Molecular Biology. Recurrent topics in Elliott H. Sherr's work include Fetal and Pediatric Neurological Disorders (41 papers), Genomic variations and chromosomal abnormalities (27 papers) and Genetics and Neurodevelopmental Disorders (23 papers). Elliott H. Sherr is often cited by papers focused on Fetal and Pediatric Neurological Disorders (41 papers), Genomic variations and chromosomal abnormalities (27 papers) and Genetics and Neurodevelopmental Disorders (23 papers). Elliott H. Sherr collaborates with scholars based in United States, Australia and United Kingdom. Elliott H. Sherr's co-authors include Pratik Mukherjee, A. James Barkovich, Linda J. Richards, Lynn K. Paul, Warren S. Brown, Mari Wakahiro, Ralph Adolphs, J. Michael Tyszka, Polina Bukshpun and Srikantan S. Nagarajan and has published in prestigious journals such as Journal of Clinical Investigation, Neuron and The Journal of Experimental Medicine.

In The Last Decade

Elliott H. Sherr

104 papers receiving 4.8k 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.

Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity

2007 588 citations Linda J. Richards, Pratik Mukherjee et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elliott H. Sherr United States	41	1.8k	1.6k	1.4k	1.2k	1.0k	104	5.0k
Richard J. Leventer Australia	37	1.5k 0.8×	1.4k 0.9×	1.8k 1.2×	273 0.2×	350 0.3×	142	4.8k
Coriene E. Catsman‐Berrevoets Netherlands	41	1.0k 0.6×	308 0.2×	857 0.6×	862 0.7×	511 0.5×	142	5.6k
Jacob Ellegood Canada	32	293 0.2×	1.2k 0.7×	1.2k 0.8×	1.1k 1.0×	297 0.3×	90	3.0k
Michele D. Poe United States	35	503 0.3×	1.4k 0.8×	908 0.6×	3.1k 2.7×	201 0.2×	71	6.1k
Nadia Bahi‐Buisson France	36	747 0.4×	3.1k 1.9×	2.4k 1.7×	1.3k 1.1×	102 0.1×	150	5.6k
Ingeborg Krägeloh‐Mann Germany	42	2.2k 1.2×	249 0.2×	1.3k 0.9×	1.1k 0.9×	689 0.7×	178	6.1k
Theodore P. Rasmussen United States	39	455 0.2×	871 0.5×	3.0k 2.1×	2.4k 2.1×	327 0.3×	91	7.1k
Anne S. Bassett Canada	54	576 0.3×	4.8k 2.9×	6.2k 4.3×	1.4k 1.2×	203 0.2×	209	10.1k
Daria Riva Italy	31	876 0.5×	412 0.3×	489 0.3×	1.2k 1.0×	310 0.3×	112	4.0k
Dawna L. Armstrong United States	43	1.4k 0.8×	2.1k 1.3×	4.1k 2.8×	1.3k 1.1×	150 0.1×	78	8.8k

Countries citing papers authored by Elliott H. Sherr

Since Specialization

Citations

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

Fields of papers citing papers by Elliott H. Sherr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elliott H. Sherr. 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 Elliott H. Sherr. The network helps show where Elliott H. Sherr may publish in the future.

Co-authorship network of co-authors of Elliott H. Sherr

This figure shows the co-authorship network connecting the top 25 collaborators of Elliott H. Sherr. A scholar is included among the top collaborators of Elliott H. Sherr 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 Elliott H. Sherr. Elliott H. Sherr 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

Kundu, Shinjini, Haris I. Sair, Elliott H. Sherr, Pratik Mukherjee, & Gustavo K. Rohde. (2024). Discovering the gene-brain-behavior link in autism via generative machine learning. Science Advances. 10(24). eadl5307–eadl5307. 4 indexed citations

Gano, Dawn, Andrea C. Pardo, Orit A. Glenn, & Elliott H. Sherr. (2024). Diverse childhood neurologic disorders and outcomes following fetal neurologic consultation. Seminars in Fetal and Neonatal Medicine. 29(1). 101524–101524. 1 indexed citations

Li, Jiang, et al.. (2024). Modulating the unfolded protein response with ISRIB mitigates cisplatin ototoxicity. Scientific Reports. 14(1). 22382–22382. 3 indexed citations

Li, Jiang, et al.. (2024). Noise induces Ca2+ signaling waves and Chop/S-Xbp1 expression in the hearing cochlea. JCI Insight. 10(2). 3 indexed citations

Nakashima, Mitsuko, et al.. (2022). De novo CLCN3 variants affecting Gly327 cause severe neurodevelopmental syndrome with brain structural abnormalities. Journal of Human Genetics. 68(4). 291–298. 1 indexed citations

Morcom, Laura, Timothy J. Edwards, Dorothy M. Jones, et al.. (2021). DRAXIN regulates interhemispheric fissure remodelling to influence the extent of corpus callosum formation. eLife. 10. 10 indexed citations

Michelson, Marina, Emanuela Argilli, Keren Yosovich, et al.. (2021). Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders. Journal of Human Genetics. 67(2). 95–101. 2 indexed citations

Parker, Karen J., Joseph P. Garner, Ozge Oztan, et al.. (2018). Arginine vasopressin in cerebrospinal fluid is a marker of sociality in nonhuman primates. Science Translational Medicine. 10(439). 45 indexed citations

Sclafani, Valentina, et al.. (2016). Early Predictors of Impaired Social Functioning in Male Rhesus Macaques (Macaca mulatta). PLoS ONE. 11(10). e0165401–e0165401. 39 indexed citations

10.

Berman, Jeffrey, Lisa Blaskey, Emily S. Kuschner, et al.. (2016). Relationship between M100 Auditory Evoked Response and Auditory Radiation Microstructure in 16p11.2 Deletion and Duplication Carriers. American Journal of Neuroradiology. 37(6). 1178–1184. 18 indexed citations

11.

Barkovich, James, et al.. (2014). De novo ANKRD11 and KDM1A gene mutations in a male with features of KBG syndrome and Kabuki syndrome. American Journal of Medical Genetics Part A. 164(7). 1744–1749. 60 indexed citations

12.

Owen, Julia P., Yi‐Ou Li, Fan Yang, et al.. (2013). Resting-State Networks and the Functional Connectome of the Human Brain in Agenesis of the Corpus Callosum. Brain Connectivity. 3(6). 547–562. 44 indexed citations

13.

Owen, Julia P., Etay Ziv, Polina Bukshpun, et al.. (2013). Test–Retest Reliability of Computational Network Measurements Derived from the Structural Connectome of the Human Brain. Brain Connectivity. 3(2). 160–176. 65 indexed citations

14.

Jones, Dorothy M., Mu Yang, Nathan Osbun, et al.. (2013). Quantitative Trait Loci for Interhemispheric Commissure Development and Social Behaviors in the BTBR T+ tf/J Mouse Model of Autism. PLoS ONE. 8(4). e61829–e61829. 46 indexed citations

15.

Akizu, Naiara, Tawfeg Ben‐Omran, Lailá Bastaki, et al.. (2013). Whole-Exome Sequencing Identifies Mutated C12orf57 in Recessive Corpus Callosum Hypoplasia. The American Journal of Human Genetics. 92(3). 392–400. 19 indexed citations

16.

Su, Shu-Yi, Jay Kasberger, Sergio E. Baranzini, et al.. (2012). Detection of identity by descent using next-generation whole genome sequencing data. BMC Bioinformatics. 13(1). 121–121. 11 indexed citations

17.

Michelson, David, Michael Shevell, Elliott H. Sherr, et al.. (2011). Evidence Report: Genetic and metabolic testing on children with global developmental delay [RETIRED]. Neurology. 77(17). 1629–1635. 168 indexed citations

18.

Glass, Hannah C., Gary M. Shaw, Chen Ma, & Elliott H. Sherr. (2008). Agenesis of the corpus callosum in California 1983–2003: A population‐based study. American Journal of Medical Genetics Part A. 146A(19). 2495–2500. 170 indexed citations

19.

Hetts, Steven W., et al.. (2006). Anomalies of the Corpus Callosum: An MR Analysis of the Phenotypic Spectrum of Associated Malformations. American Journal of Roentgenology. 187(5). 1343–1348. 137 indexed citations

20.

Saxon, Andrew, Janis V. Giorgi, Elliott H. Sherr, & J. Kagan. (1989). Failure of B cells in common variable immunodeficiency to transit from proliferation to differentiation is associated with altered B cell surface-molecule display. Journal of Allergy and Clinical Immunology. 84(1). 44–55. 28 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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