John Herriges

539 total citations
18 papers, 302 citations indexed

About

John Herriges is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, John Herriges has authored 18 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Surgery. Recurrent topics in John Herriges's work include Genomic variations and chromosomal abnormalities (5 papers), Neonatal Respiratory Health Research (4 papers) and Genomics and Rare Diseases (3 papers). John Herriges is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Neonatal Respiratory Health Research (4 papers) and Genomics and Rare Diseases (3 papers). John Herriges collaborates with scholars based in United States and China. John Herriges's co-authors include Xin Sun, Jamie M. Verheyden, Mark Lewandoski, Zhen Zhang, Matthew J. Anderson, Deborah A. Swing, Yan Zhang, Ying Zhang, Pengfei Sui and Robert P. Mecham and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

John Herriges

18 papers receiving 298 citations

Peers

Countries citing papers authored by John Herriges

Since Specialization

Citations

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

Fields of papers citing papers by John Herriges

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John Herriges

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

#	Work	Indexed citations
1	Hyperinsulinemic Hypoglycemia and Growth Hormone Deficiency Secondary to 20p11 Deletion 2023 ·SHILAP Revista de lepidopterología ·(unknown), John Herriges, (unknown), Sarah L. Tsai, Joseph T. Alaimo, (unknown)	3
2	Integrated genetic profiling of archival pediatric high-grade glial tumors and reassessment with 2021 WHO classification of paediatric CNS tumours 2023 ·Cancer Genetics ·Linda D. Cooley, (unknown), (unknown), John Herriges, Lei Zhang, Elena Repnikova, Julie M. Joyce, (unknown), (unknown), Scott C. Smith, Byunggil Yoo, (unknown), Kevin Ginn, Midhat S. Farooqi	2
3	P457: A case of hexasomy 15q due to a tricentric supernumerary chromosome 15 2023 ·SHILAP Revista de lepidopterología ·Emily Farrow, Laura Cross, Bonnie Sullivan, (unknown), Ahmed Abdelmoity, Joseph T. Alaimo, Elena Repnikova, John Herriges, Lei Zhang	1
4	Clinical Validation of Genome Reference Consortium Human Build 38 in a Laboratory Utilizing Next-Generation Sequencing Technologies 2022 ·Clinical Chemistry ·(unknown), Maxime Cadieux‐Dion, John Herriges, Jeffrey Johnston, Byunggil Yoo, Joseph T. Alaimo, Isabelle Thiffault, Neil Miller, Ana S.A. Cohen, Elena Repnikova, Lei Zhang, Midhat S. Farooqi, Emily Farrow, Carol Saunders	4
5	Factors Affecting Migration to GRCh38 in Laboratories Performing Clinical Next-Generation Sequencing 2021 ·Journal of Molecular Diagnostics ·(unknown), Maxime Cadieux‐Dion, Byunggil Yoo, Neil Miller, Ana S.A. Cohen, Lee Zellmer, (unknown), Emily Farrow, Isabelle Thiffault, Elena Repnikova, Linda D. Cooley, Joseph T. Alaimo, Binu Porath, John Herriges, Carol Saunders, Midhat S. Farooqi	12
6	Clinical and molecular cytogenetic characterization of a novel 10q interstitial deletion: a case report and review of the literature 2019 ·Molecular Cytogenetics ·John Herriges, Sarah Dugan, Allen N. Lamb	1
7	Neuroblastoma in Adolescents and Children Older than 10 Years: Unusual Clinicopathologic and Biologic Features 2019 ·Journal of Pediatric Hematology/Oncology ·(unknown), Katherine Chastain, (unknown), Eugenio Taboada, Robert E. Garola, John Herriges, Linda D. Cooley, Atif Ahmed	4
8	Identification of two 14q32 deletions involving DICER1 associated with the development of DICER1-related tumors 2018 ·European Journal of Medical Genetics ·John Herriges, (unknown), (unknown), Jillian R. Ozmore, John B. Moeschler, (unknown), Jeanne Meck, Sarah T. South, Erica Andersen	16
9	28. Dosage sensitivity curation of recurrent copy number variant regions 2018 ·Cancer Genetics ·Erica Andersen, Rachel D. Burnside, Bradley P. Coe, Laura K. Conlin, John Herriges, (unknown), Benjamin Hilton, Vaidehi Jobanputra, Hutton M. Kearney, Karen Ouyang, (unknown), Erin Rooney Riggs, Ross Rowsey, Marsha Speevak, Erik C. Thorland, Lei Zhang, Christa Lese Martin	1
10	Delineating the Clinical Spectrum Associated With Xq25q26.2 Duplications: Report of 2 Families and Review of the Literature 2018 ·Journal of Child Neurology ·John Herriges, (unknown), (unknown), Erin E. Baldwin, Danielle LaGrave, Allen N. Lamb, Reha M. Toydemir	1
11	FGF receptors control alveolar elastogenesis 2017 ·Development ·Rongbo Li, John Herriges, Lin Chen, Robert P. Mecham, Xin Sun	34
12	Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder 2016 ·European Journal of Medical Genetics ·(unknown), Danielle LaGrave, Alison Millson, John Herriges, Allen N. Lamb, Reuben Matalon	19
13	Syndactyly in a novel Fras1^rdf mutant results from interruption of signals for interdigital apoptosis 2016 ·Developmental Dynamics ·Elizabeth A Hines, Jamie M. Verheyden, (unknown), (unknown), (unknown), Eric T. Domyan, Juan Gao, (unknown), John Herriges, Linghan Hu, David J. McCulley, Kurt Throckmorton, Shigetoshi Yokoyama, Akihiro Ikeda, Guoliang Xu, Xin Sun	6
14	E3 ubiquitin ligase RFWD2 controls lung branching through protein-level regulation of ETV transcription factors 2016 ·Proceedings of the National Academy of Sciences ·Yan Zhang, Shigetoshi Yokoyama, John Herriges, Zhen Zhang, Randee E. Young, Jamie M. Verheyden, Xin Sun	31
15	Ontogeny of the mouse vocal fold epithelium 2015 ·Developmental Biology ·Vlasta Lungová, Jamie M. Verheyden, John Herriges, Xin Sun, Susan L. Thibeault	37
16	FGF-Regulated ETV Transcription Factors Control FGF-SHH Feedback Loop in Lung Branching 2015 ·Developmental Cell ·John Herriges, Jamie M. Verheyden, Zhen Zhang, Pengfei Sui, Ying Zhang, Matthew J. Anderson, Deborah A. Swing, Yan Zhang, Mark Lewandoski, Xin Sun	80
17	Genome‐scale study of transcription factor expression in the branching mouse lung 2012 ·Developmental Dynamics ·John Herriges, (unknown), Elizabeth A Hines, (unknown), Guoliang Xu, Paul A. Gray, Qiufu Ma, Xin Sun	33
18	An Evolutionarily Conserved Arginine Is Essential for Tre1 G Protein-Coupled Receptor Function During Germ Cell Migration in Drosophila melanogaster 2010 ·PLoS ONE ·(unknown), Margaret Pruitt, John Herriges, Clark R. Coffman	17

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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