Newell Belnap

748 total citations
12 papers, 126 citations indexed

About

Newell Belnap is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Newell Belnap has authored 12 papers receiving a total of 126 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Newell Belnap's work include Genomics and Rare Diseases (4 papers), RNA regulation and disease (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Newell Belnap is often cited by papers focused on Genomics and Rare Diseases (4 papers), RNA regulation and disease (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Newell Belnap collaborates with scholars based in United States. Newell Belnap's co-authors include Vinodh Narayanan, Keri Ramsey, Isabelle Schrauwen, Sampathkumar Rangasamy, Ashley L. Siniard, Ryan Richholt, Szabolcs Szelinger, Ana M. Claasen, Matthew J. Huentelman and Matt De Both and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Scientific Reports.

In The Last Decade

Newell Belnap

10 papers receiving 124 citations

Peers

Countries citing papers authored by Newell Belnap

Since Specialization

Citations

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

Fields of papers citing papers by Newell Belnap

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Newell Belnap

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

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Expanded carrier screening for inherited genetic disease using exome and genome sequencing 2024 ·Journal of Genetic Counseling ·Newell Belnap, Keri Ramsey, Alon Abraham, Aidan Ryan, Sampathkumar Rangasamy, (unknown), Marcus Naymik, Matthew J. Huentelman, Sara S. Strom, David J. Perry, Akila Subramaniam, W W Grody, Szabolcs Szelinger, Vinodh Narayanan	0
2	Exploring the Frontier: The Human Microbiome’s Role in Rare Childhood Neurological Diseases and Epilepsy 2024 ·Brain Sciences ·Newell Belnap, Keri Ramsey, (unknown), (unknown), (unknown), Matthew J. Huentelman, Keehoon Lee	1
3	Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: A novel SMS gene variant 2023 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), Newell Belnap, Marcus Naymik, (unknown), Jennifer L. Sloan, (unknown), (unknown), (unknown), Tracy Murray Stewart, Jackson R. Foley, Sampathkumar Rangasamy, Matthew J. Huentelman, Vinodh Narayanan, Keri Ramsey	2
4	Improved methods for RNAseq-based alternative splicing analysis 2021 ·Scientific Reports ·Rebecca F. Halperin, Apurva M. Hegde, Jessica D. Lang, (unknown), Vinodh Narayanan, Matt Huentelman, Newell Belnap, (unknown), Keri Ramsey, Christophe Legendre, Winnie S. Liang, Patricia LoRusso, Aleksandar Sekulić, Jeffrey A. Sosman, Jeffrey M. Trent, Sampathkumar Rangasamy, Patrick Pirrotte, Nicholas J. Schork	26
5	Progressive bilateral nuclear cataracts associated with cerebellar-facial-dental syndrome: case report, literature review, and identification of a new genetic variant 2021 ·Journal of American Association for Pediatric Ophthalmology and Strabismus ·(unknown), Newell Belnap, Chris Balak, Matt Huentelman, Keri Ramsey, Vinodh Narayanan, (unknown)	0
6	Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex 2020 ·Nature Communications ·Jinhong Wie, (unknown), (unknown), Vinodh Narayanan, Keri Ramsey, Newell Belnap, Ana M. Claasen, Amanda Courtright, Matt De Both, Matthew J. Huentelman, Sampathkumar Rangasamy, Ryan Richholt, Isabelle Schrauwen, Ashley L. Siniard, (unknown), Kimberly Aranda, Qi Zhang, Yandong Zhou, Dejian Ren	19
7	Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD) 2019 ·Human Genetics ·Lorida Llaci, Keri Ramsey, Newell Belnap, Ana M. Claasen, Chris Balak, Szabolcs Szelinger, (unknown), Ashley L. Siniard, Ryan Richholt, (unknown), Marcus Naymik, Matt De Both, Ignazio S. Piras, David W. Craig, Matthew J. Huentelman, Vinodh Narayanan, Isabelle Schrauwen, Sampathkumar Rangasamy	12
8	Utilizing RNA and outlier analysis to identify an intronic splice‐altering variant inAP4S1in a sibling pair with progressive spastic paraplegia 2019 ·Human Mutation ·(unknown), Szabolcs Szelinger, Newell Belnap, Keri Ramsey, Isabelle Schrauwen, Ana M. Claasen, Leah W. Burke, Ashley L. Siniard, Matthew J. Huentelman, Vinodh Narayanan, David W. Craig	5
9	Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results 2017 ·Seminars in Pediatric Neurology ·(unknown), Keri Ramsey, Newell Belnap, Szabolcs Szelinger, Ashley L. Siniard, Chris Balak, Megan Russell, Ryan Richholt, Matt De Both, Ana M. Claasen, Isabelle Schrauwen, Matthew J. Huentelman, David W. Craig, Sampathkumar Rangasamy, Vinodh Narayanan	9
10	A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2 , a Gene Encoding a Component of the TTT Complex 2016 ·The American Journal of Human Genetics ·Jing You, Nara Sobreira, Dustin L. Gable, Julie A. Jurgens, Dorothy K. Grange, Newell Belnap, Ashley L. Siniard, Szabolcs Szelinger, Isabelle Schrauwen, Ryan Richholt, Stephanie E. Vallee, Mary Beth Dinulos, David Valle, Mary Armanios, Julie Hoover‐Fong	26
11	An atypical presentation of ACAD9 deficiency: Diagnosis by whole exome sequencing broadens the phenotypic spectrum and alters treatment approach 2016 ·Molecular Genetics and Metabolism Reports ·(unknown), Vinodh Narayanan, Newell Belnap, Keri Ramsey, Theresa A. Grebe	11
12	A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia 2016 ·Molecular Case Studies ·(unknown), Newell Belnap, Ashley L. Siniard, Szabolcs Szelinger, Ana M. Claasen, Ryan Richholt, Matt De Both, Jason J. Corneveaux, Chris Balak, Ignazio S. Piras, Megan Russell, (unknown), Sampathkumar Rangasamy, Keri Ramsey, David W. Craig, Vinodh Narayanan, Matt Huentelman, Isabelle Schrauwen	15

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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