Andrew O.M. Wilkie

Also affiliated with John Radcliffe Hospital, University of Oxford, MRC Weatherall Institute of Molecular Medicine

Biochemistry, Genetics and Molecular Biology

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 8 papers. Top paper: “SMAD6 variants in craniosynostosis: genotype and phenotype evaluation”.

SMAD6 variants in craniosynostosis: genotype and phenotype evaluation

Genetics in Medicine(2020)10.1038/s41436-020-0817-2

N/A

0DataRank · unranked

51 citations

Araceli Cuellar, Krithi Bala, Sigrid M. A. Swagemakers, Nils Koelling, Simon J. McGowan +19 more

The developing mouse coronal suture at single-cell resolution

Nature Communications(2021)10.1038/s41467-021-24917-9

N/A

0DataRank · unranked

101 citations

Hana Mlčochová, Yan Zhou, Nils Koelling, Guanlin Wang, Neil Ashley +10 more

Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders

Journal of Medical Genetics(2021)10.1136/jmedgenet-2020-107459

N/A

0DataRank · unranked

10 citations

Maud Wurmser, Simon J. McGowan, Rodrigo Atique, Débora Romeo Bertola, Michael L. Cunningham +11 more

The developing mouse coronal suture at single-cell resolution

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.24.432636

N/A

0DataRank · unranked

9 citations

Hana Mlčochová, Yan Zhou, Nils Koelling, Guanlin Wang, Neil Ashley +5 more

The p190 RhoGAPs, ARHGAP35, and ARHGAP5 are implicated in GnRH neuronal development: Evidence from patients with idiopathic hypogonadotropic hypogonadism, zebrafish, and in vitro GAP activity assay

Genetics in Medicine(2022)10.1016/j.gim.2022.08.025

N/A

0DataRank · unranked

8 citations

Wanxue Xu, Abigail A Smith, Xinyu Miao, Agathe Lafont, Omar Shennib +23 more

BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome

Journal of Medical Genetics(2024)10.1136/jmg-2023-109531

N/A

0DataRank · unranked

12 citations

David A. Cruz Walma, Daniel M. Pinkas, Rebecca S Tooze, Joshua C. Bufton, William Richardson +13 more

Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101851

N/A

0DataRank · unranked

4 citations

Samreen Zafer, Lital Matok, Inbar Irron, Meidva Patrick, Rotem Haklai +72 more

Identification and characterization of short-chain dehydrogenase/reductase 3 (DHRS3) deficiency, a retinoic acid embryopathy of humans

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103427

N/A

0DataRank · unranked

1 citations

Jianshi Yu, Christina Williams, Karin Gaudenz, Parisa Varshosaz, Ruonan Zhao +25 more