Richard Sidlow

Biochemistry, Genetics and Molecular BiologyNeuroscience

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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 9 papers. Top paper: “DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders”.

DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.012

N/A

0.292DataRank · unranked

6 citations

Anja Barešić, Iván K. Chinn, Jonathan May, Anu Goenka, Kate Chandler +91 more

Sequence variants in HECTD1 result in a variable neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.001

N/A

0.241DataRank · unranked

4 citations

Elias Oxman, Hieu D. Hoang, Wu‐Lin Charng, Tanvitha Kotla, Weimin Yuan +49 more

Conifer metabolite pisiferic acid restores activity in human Kv1.2 potassium channels carrying pathogenic sequence variants

iScience(2025)10.1016/j.isci.2025.113283

N/A

0.208DataRank · unranked

3 citations

Richard Sidlow, Geoffrey W. Abbott, Rían W. Manville

A novel autism-associated KCNB1 mutation dramatically slows Kv2.1 potassium channel activation, deactivation and inactivation

Frontiers in Cellular Neuroscience(2024)10.3389/fncel.2024.1438101

N/A

0DataRank · unranked

7 citations

Samantha D. Block, Claire L. Illeck, Jessica Kottmeier, Richard Sidlow, Geoffrey W. Abbott +1 more

A novel loss-of-function KCNB1 gene variant in a twin with global developmental delay and seizures

Frontiers in Cellular Neuroscience(2024)10.3389/fncel.2024.1477989

N/A

0DataRank · unranked

0 citations

Claire L. Illeck, César Miguel Momesso, Richard Sidlow, Geoffrey W. Abbott, Rían W. Manville

Case report: A novel loss-of-function pathogenic variant in the KCNA1 cytoplasmic N-terminus causing carbamazepine-responsive type 1 episodic ataxia

Frontiers in Neurology(2022)10.3389/fneur.2022.975849

N/A

0DataRank · unranked

8 citations

Richard Sidlow, Geoffrey W. Abbott, Rían W. Manville

DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders

UNC Libraries(2025)10.17615/dy6f-xt03

N/A

0DataRank · unranked

0 citations

Benjamin Cogné, Rachel Rabin, E Kessler, Céline Chappé, Melanie Brügger +92 more

Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.11.007

N/A

0DataRank · unranked

37 citations

María J. Guillen Sacoto, Francisca Millan, Zhancheng Zhang, Stephen McGee, Matthew T. Oetjens +11 more

Native American ataxia medicines rescue ataxia-linked mutant potassium channel activity via binding to the voltage sensing domain

Nature Communications(2023)10.1038/s41467-023-38834-6

N/A

0DataRank · unranked

14 citations

J. Alfredo Freites, Richard Sidlow, Douglas J. Tobias, Geoffrey W. Abbott, Rían W. Manville