Julie R. Jones

Biochemistry, Genetics and Molecular BiologyArts and Humanities

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 7 papers. Top paper: “BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder”.

BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder

Human Mutation(2020)10.1002/humu.23992

N/A

0.961DataRank · unranked

28 citations

Hui Guo, Evan E. Eichler, Jill A. Rosenfeld, Kaifang Pang, Zhandong Liu +20 more

Practical challenges for functional validation of STAT1 gain of function genetic variants

Clinical & Experimental Immunology(2023)10.1093/cei/uxad008

N/A

0.208DataRank · unranked

3 citations

Jesmeen Maimaris, Alexander J McKenna, Jonathan Lambourne, Fernando Moreira, Sarita Workman +91 more

SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance

Human Molecular Genetics(2022)10.1093/hmg/ddac114

N/A

0DataRank · unranked

17 citations

Martina Schaettin, Médéric Jeanne, Veranika Panasenkava, Anne‐Sophie Denommé‐Pichon, Boris Keren +43 more

De Novo Variants in LMNB1 Cause Pronounced Syndromic Microcephaly and Disruption of Nuclear Envelope Integrity

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.08.015

N/A

0DataRank · unranked

43 citations

Tonya Moss, Hannah W. Moore, Koenraad Devriendt, Heather Flanagan‐Steet, Melanie May +15 more

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.01.013

N/A

0DataRank · unranked

25 citations

Eva Jacobs, Lies Vantomme, Pontus LeBlanc, Elke Bogaert, Annelies Dheedene +95 more

A clinical and genotype-phenotype analysis of MACF1 variants

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.010

N/A

0DataRank · unranked

1 citations

Rachel Schot, Kimberly A. Aldinger, David B. Everman, Camerun Washington, Julie R. Jones +85 more

Expanding the clinical and metabolic phenotype of DPM2 deficient congenital disorders of glycosylation

Molecular Genetics and Metabolism(2020)10.1016/j.ymgme.2020.10.007

N/A

0DataRank · unranked

25 citations

Taylor Fitzpatrick‐Schmidt, Seul Kee Byeon, Anil K. Madugundu, Mayank Saraswat, Angie Lichty +13 more