Logan C. Walker

Biochemistry, Genetics and Molecular BiologyMedicine

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 11 papers. Top paper: “Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup”.

Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.002

N/A

6.1DataRank · unranked

324 citations

Miguel de la Hoya, George A. R. Wiggins, Amanda Lindy, Lisa M. Vincent, Michael T. Parsons +28 more

Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.013

N/A

0.689DataRank · unranked

98 citations

Miguel de la Hoya, Marcy E. Richardson, Emma Tudini, Michael Anderson, Windy Berkofsky-Fessler +38 more

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.08.022

N/A

0.434DataRank · unranked

17 citations

Megan Holdren, Terra Brannan, Miguel de la Hoya, Amanda B. Spurdle, Sean V. Tavtigian +16 more

Rare germline copy number variants (CNVs) and breast cancer risk

Communications Biology(2022)10.1038/s42003-021-02990-6

N/A

0.416DataRank · unranked

15 citations

Jonathan P. Tyrer, Logan C. Walker, Kyriaki Michailidou, Leila Dorling, Manjeet K. Bolla +94 more

Detecting rare copy number variants from Illumina genotyping arrays with the CamCNV pipeline: Segmentation of z ‐scores improves detection and reliability

Genetic Epidemiology(2020)10.1002/gepi.22367

N/A

0.406DataRank · unranked

14 citations

Logan C. Walker, Jonathan P. Tyrer, Kyriaki Michailidou, Douglas F. Easton, Joe Dennis

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline PALB2 sequence variants

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.020

N/A

0.241DataRank · unranked

4 citations

Megan F.H. Bishop, Megan Holdren, Miguel de la Hoya, Amanda B. Spurdle, Sean V. Tavtigian +15 more

Germline copy number variants and endometrial cancer risk

Human Genetics(2024)10.1007/s00439-024-02707-9

N/A

0.225DataRank · unranked

3 citations

George A. R. Wiggins, V. Lau, Joe Dennis, Andrew N. Shelling, Michelle Wilson +45 more

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants

medRxiv(2024)10.1101/2024.05.28.24307502

N/A

0.165DataRank · unranked

2 citations

Megan Holdren, Terra Brannan, Miguel de la Hoya, Amanda B. Spurdle, Sean V. Tavtigian +16 more

APPLICATION OF THE ACMG/AMP FRAMEWORK TO CAPTURE EVIDENCE RELEVANT TO PREDICTED AND OBSERVED IMPACT ON SPLICING: RECOMMENDATIONS FROM THE CLINGEN SVI SPLICING SUBGROUP

medRxiv(2023)10.1101/2023.02.24.23286431

N/A

0DataRank · unranked

17 citations

Miguel de la Hoya, George A. R. Wiggins, Amanda Lindy, Lisa M. Vincent, Michael T. Parsons +11 more

Rare copy number variants (CNVs) and breast cancer risk

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.20.444828

N/A

0DataRank · unranked

0 citations

Jonathan P. Tyrer, Logan C. Walker, Kyriaki Michailidou, Leila Dorling, Manjeet K. Bolla +95 more

Rare Copy Number Variants (CNVs) and Breast Cancer Risk

Research Square(2021)10.21203/rs.3.rs-602209/v1

N/A

0DataRank · unranked

0 citations

Jonathan P. Tyrer, Logan C. Walker, Kyriaki Michailidou, Leila Dorling, Manjeet Bola +95 more