Eric M. Morrow

15.1k total citations · 2 hit papers
79 papers, 4.8k citations indexed

About

Eric M. Morrow is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Eric M. Morrow has authored 79 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 42 papers in Genetics and 26 papers in Cognitive Neuroscience. Recurrent topics in Eric M. Morrow's work include Genetics and Neurodevelopmental Disorders (31 papers), Autism Spectrum Disorder Research (24 papers) and Genomic variations and chromosomal abnormalities (19 papers). Eric M. Morrow is often cited by papers focused on Genetics and Neurodevelopmental Disorders (31 papers), Autism Spectrum Disorder Research (24 papers) and Genomic variations and chromosomal abnormalities (19 papers). Eric M. Morrow collaborates with scholars based in United States, Germany and Russia. Eric M. Morrow's co-authors include Constance L. Cepko, Takahisa Furukawa, Fred C. Davis, T Li, Zheng‐Zheng Bao, Siddhartha Mukherjee, Jacqueline E. Lee, Matthew F. Pescosolido, Christopher A. Walsh and Brett S. Abrahams and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Neuron.

In The Last Decade

Eric M. Morrow

75 papers receiving 4.7k 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.

Crx, a Novel otx-like Homeobox Gene, Shows Photoreceptor-Specific Expression and Regulates Photoreceptor Differentiation

1997 730 citations Takahisa Furukawa, Eric M. Morrow et al. Cell profile →
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

2013 495 citations Brett S. Abrahams, Dan E. Arking et al. Molecular Autism profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eric M. Morrow United States	30	3.1k	1.3k	1.2k	1.1k	543	79	4.8k
Alessandro Cellerino Italy	46	2.5k 0.8×	397 0.3×	1.6k 1.4×	327 0.3×	459 0.8×	134	6.2k
Noriko Osumi Japan	53	6.2k 2.0×	1.7k 1.3×	1.8k 1.5×	301 0.3×	774 1.4×	223	9.0k
Andrew D. Huberman United States	41	4.2k 1.4×	465 0.4×	4.3k 3.6×	1.8k 1.7×	489 0.9×	66	8.6k
Jun Aruga Japan	47	5.6k 1.8×	1.6k 1.2×	1.6k 1.3×	299 0.3×	1.1k 2.1×	115	7.5k
Patrick Callaerts Belgium	42	4.0k 1.3×	1.3k 1.0×	1.6k 1.4×	168 0.2×	528 1.0×	110	6.4k
Jacques L. Michaud Canada	44	4.0k 1.3×	2.5k 1.9×	747 0.6×	441 0.4×	652 1.2×	124	6.8k
Thomas Becker Germany	55	3.8k 1.2×	745 0.6×	2.4k 2.1×	318 0.3×	2.6k 4.9×	199	8.3k
Glen Jeffery United Kingdom	43	3.4k 1.1×	225 0.2×	1.7k 1.5×	431 0.4×	875 1.6×	171	5.4k
Ronald G. Gregg United States	46	5.4k 1.7×	1.1k 0.9×	2.6k 2.3×	152 0.1×	725 1.3×	132	7.1k
Beth Burnside United States	39	2.6k 0.9×	268 0.2×	1.3k 1.1×	275 0.3×	1.4k 2.6×	99	5.0k

Countries citing papers authored by Eric M. Morrow

Since Specialization

Citations

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

Fields of papers citing papers by Eric M. Morrow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric M. Morrow. 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 Eric M. Morrow. The network helps show where Eric M. Morrow may publish in the future.

Co-authorship network of co-authors of Eric M. Morrow

This figure shows the co-authorship network connecting the top 25 collaborators of Eric M. Morrow. A scholar is included among the top collaborators of Eric M. Morrow 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 Eric M. Morrow. Eric M. Morrow 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

Davidson, Shawn M., et al.. (2024). Loss of mitochondrial enzyme GPT2 leads to reprogramming of synaptic glutamate metabolism. Molecular Brain. 17(1). 87–87.

Ma, Li, et al.. (2024). GGA1 interacts with the endosomal Na+/H+ exchanger NHE6 governing localization to the endosome compartment. Journal of Biological Chemistry. 300(8). 107552–107552.

Lizarraga, Sofia B., Li Ma, Laura I. van Dyck, et al.. (2021). Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Science Translational Medicine. 13(580). 20 indexed citations

Schmitz‐Abe, Klaus, Guzman Sánchez‐Schmitz, Ryan N. Doan, et al.. (2020). Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Scientific Reports. 10(1). 14045–14045. 13 indexed citations

Ouyang, Qing, Brian C. Kavanaugh, Lena Joesch-Cohen, et al.. (2019). GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates. Human Genetics. 138(10). 1183–1200. 6 indexed citations

Ouyang, Qing, et al.. (2019). Functional AssessmentIn Vivoof the Mouse Homolog of the Human Ala-9-Ser NHE6 Variant. eNeuro. 6(6). ENEURO.0046–19.2019. 5 indexed citations

Xu, Meiyu, Qing Ouyang, Jingyi Gong, et al.. (2017). Mixed Neurodevelopmental and Neurodegenerative Pathology inNhe6-Null Mouse Model of Christianson Syndrome. eNeuro. 4(6). ENEURO.0388–17.2017. 19 indexed citations

Wink, Logan, Ernest V. Pedapati, Ryan Adams, et al.. (2017). Characterization of Medication Use in a Multicenter Sample of Pediatric Inpatients with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. 48(11). 3711–3719. 12 indexed citations

Gerber, Alan S., Carolyn E. B. McCormick, Todd P. Levine, et al.. (2017). Brief Report: Factors Influencing Healthcare Satisfaction in Adults with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. 47(6). 1896–1903. 16 indexed citations

10.

Dyck, Laura I. van & Eric M. Morrow. (2016). Genetic control of postnatal human brain growth. Current Opinion in Neurology. 30(1). 114–124. 46 indexed citations

11.

Howe, Yamini J., et al.. (2015). Female Autism Phenotypes Investigated at Different Levels of Language and Developmental Abilities. Journal of Autism and Developmental Disorders. 45(11). 3537–3549. 51 indexed citations

12.

Harrison, Ashley J., et al.. (2014). Observation-centered Approach to ASD Assessment in Tanzania. Intellectual and developmental disabilities. 52(5). 330–347. 13 indexed citations

13.

Uzun, Ece D. Gamsiz, Emma Viscidi, A. Matsen Frederick, et al.. (2013). Intellectual Disability Is Associated with Increased Runs of Homozygosity in Simplex Autism. The American Journal of Human Genetics. 93(1). 103–109. 52 indexed citations

14.

Abrahams, Brett S., Dan E. Arking, Jerry L. Campbell, et al.. (2013). SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs). Molecular Autism. 4(1). 36–36. 495 indexed citations breakdown →

15.

Pescosolido, Matthew F., et al.. (2013). An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma. American Journal of Medical Genetics Part A. 161(4). 787–791. 22 indexed citations

16.

Uzun, Ece D. Gamsiz, Qing Ouyang, M Schmidt, Shailender Nagpal, & Eric M. Morrow. (2011). Genome-wide transcriptome analysis in murine neural retina using high-throughput RNA sequencing. Genomics. 99(1). 44–51. 34 indexed citations

17.

Ehrlich, Stefan, Eric M. Morrow, Joshua L. Roffman, et al.. (2009). The COMT Val108/158Met polymorphism and medial temporal lobe volumetry in patients with schizophrenia and healthy adults. NeuroImage. 53(3). 992–1000. 66 indexed citations

18.

Walsh, Christopher A., Eric M. Morrow, & John L.R. Rubenstein. (2008). Autism and Brain Development. Cell. 135(3). 396–400. 144 indexed citations

19.

Morrow, Eric M., Takahisa Furukawa, Elio Raviola, & Constance L. Cepko. (2005). Synaptogenesis and outer segment formation are perturbed in the neural retina of Crx mutant mice. BMC Neuroscience. 6(1). 5–5. 55 indexed citations

20.

Morrow, Eric M., et al.. (1998). Vertebrate photoreceptor cell development and disease. Trends in Cell Biology. 8(9). 353–358. 81 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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