Robert A. Kesterson

Also affiliated with University of Alabama at Birmingham

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscienceNursing

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 15 papers. Top paper: “Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease”.

Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease

PLOS Genetics(2016)10.1371/journal.pgen.1006220

N/A

0.568DataRank · unranked

43 citations

Erik B. Malarkey, Douglas Tritschler, Raqual Bower, Raymond C. Pasek, Jonathan D. Porath +16 more

Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy

PLoS Genetics(2021)10.1371/journal.pgen.1009195

N/A

0.538DataRank · unranked

35 citations

Gopal Battu, Stephanie A. Felker, J. Nicholas Cochran, M. Newton, Laura Lambert +6 more

Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease

PMC(2020)10.17615/2swt-hn18

N/A

0DataRank · unranked

0 citations

Nicolas F. Berbari, Erik B. Malarkey, Raqual Bower, Sophie Saunier, Jonathan D. Porath +16 more

Aberrant regulation of a poison exon caused by a non-coding variant in Scn1a -associated epileptic encephalopathy

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.21.163428

N/A

0DataRank · unranked

0 citations

Gopal Battu, Stephanie A. Felker, J. Nicholas Cochran, M. Newton, Laura Lambert +6 more

Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader–Willi syndrome

UNC Libraries(2020)10.17615/05n9-rx09

N/A

0DataRank · unranked

0 citations

Robert A. Kesterson, Atheir I. Abbas, David S. Kump, Ronald B. Emeson, Michelle M. Jacobs +4 more

Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression

Scientific Reports(2021)10.1038/s41598-021-97046-4

N/A

0DataRank · unranked

21 citations

Naoe Harafuji, Amber K. O’Connor, Robert A. Kesterson, Jacob A. Watts, Amar J. Majmundar +9 more

Humanized GPRC6AKGKY is a gain-of-function polymorphism in mice

Scientific Reports(2020)10.1038/s41598-020-68113-z

N/A

0DataRank · unranked

17 citations

Fuyi Xu, Rui-Song Ye, Satoru K. Nishimoto, Robert A. Kesterson, Robert W. Williams +3 more

Restoration of Normal NF1 Function with Antisense Morpholino Treatment of Recurrent Pathogenic Patient-Specific Variant c.1466A>G; p.Y489C

Journal of Personalized Medicine(2021)10.3390/jpm11121320

N/A

0DataRank · unranked

5 citations

Marc T. Moore, Hui Liu, Lukasz Ciszewski, Laura Lambert, Bruce R. Korf +4 more

A transgenic Alx4‐CreER mouse to analyze anterior limb and nephric duct development

Developmental Dynamics(2021)10.1002/dvdy.328

N/A

0DataRank · unranked

4 citations

Amber K. O’Connor, Melissa R. Bentley‐Ford, Courtney J. Haycraft, Mandy J. Croyle, Kathryn M. Brewer +4 more

Exon Skipping as a Therapeutic for Neurofibromatosis Type I

Research Square(2021)10.21203/rs.3.rs-751331/v1

N/A

0DataRank · unranked

1 citations

André Leier, Marc T. Moore, Michael Daniel, Hui Liu, Alexis Hyde +10 more

Genomic Rearrangement in Non‐coding Region of Chromosome 1 Leads to Spontaneous Obesity and Heart Failure with Preserved Ejection Fraction

The FASEB Journal(2022)10.1096/fasebj.2022.36.s1.r5733

N/A

0DataRank · unranked

0 citations

Jian Wu, Lothar Lauterboeck, Robert A. Kesterson, Qinglin Yang, Donnell White

NF1 mutation-driven neuronal hyperexcitability sets a threshold for tumorigenesis and therapeutic targeting of murine optic glioma

Neuro-Oncology(2024)10.1093/neuonc/noae054

N/A

0DataRank · unranked

18 citations

Jit Chatterjee, Joshua P. Koleske, Yunqing Gao, Stephanie L Bozeman, Chloe M Kernan +8 more

RANK IVVY motif plays crucial roles in osteoclastogenesis

Bone(2024)10.1016/j.bone.2024.117367

N/A

0DataRank · unranked

0 citations

Zhenqi Shi, Joel Jules, Yuyu Li, Robert A. Kesterson, Mohamed Elbahoty +3 more

Functional characterization and potential therapeutic avenues for variants in the NTRK2 gene causing developmental and epileptic encephalopathies

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2021)10.1002/ajmg.b.32882

N/A

0DataRank · unranked

4 citations

Andrew B. Crouse, Robert A. Kesterson, Matthew Might, Deeann Wallis, Ashlee Long

Cystin gene mutations cause autosomal recessive polycystic kidney disease associated with altered Myc expression

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.18.946285

N/A

0DataRank · unranked

1 citations

Amber K. O’Connor, Robert A. Kesterson, Jacob A. Watts, Amar J. Majmundar, Daniela A. Braun +7 more