Jennifer B. Phillips

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: “BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms”.

BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.11.003

N/A

0DataRank · unranked

48 citations

Tahsin Stefan Barakat, Brittany C. Michel, Nazar Mashtalir, Jennifer B. Phillips, Alfredo M. Valencia +48 more

yippee like 3 (ypel3) is a novel gene required for myelinating and perineurial glia development

PLoS Genetics(2020)10.1371/journal.pgen.1008841

N/A

0DataRank · unranked

22 citations

Aurélie Clément, Sarah J. Stednitz, Jennifer Kyle, Judy Peirce, Marcie McFadden +18 more

A fish with no sex: gonadal and adrenal functions partition between zebrafishNR5A1co-orthologs

Genetics(2020)10.1093/genetics/iyaa030

N/A

0DataRank · unranked

14 citations

Tom A. Titus, Thomas Desvignes, Ruth Bremiller, Peter Batzel, Jason Sydes +12 more

COPB2 haploinsufficiency causes a coatopathy with osteoporosis and developmental delay

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.09.14.297234

N/A

0DataRank · unranked

1 citations

Lindsay C. Burrage, Aurélie Clément, Bernardo Blanco‐Sánchez, Rossella Venditti, Mahim Jain +49 more

COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.002

N/A

0DataRank · unranked

41 citations

Lindsay C. Burrage, Rossella Venditti, Aurélie Clément, Bernardo Blanco‐Sánchez, Mahim Jain +48 more

Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

Genetics in Medicine(2021)10.1038/s41436-021-01216-8

N/A

0DataRank · unranked

26 citations

Jennifer B. Phillips, Elizabeth L. Fieg, Sameer S. Bajikar, Judy Peirce, Jeremy Wegner +94 more

Erratum to: A fish with no sex: gonadal and adrenal functions partition between zebrafish NR5A1 co-orthologs

Genetics(2021)10.1093/genetics/iyab051

N/A

0DataRank · unranked

0 citations

Tom A. Titus, Thomas Desvignes, Ruth Bremiller, Peter Batzel, Jason Sydes +12 more

Deletion of Abi3 / Gngt2 influences age-progressive amyloid β and tau pathologies in distinctive ways

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.08.467701

N/A

0DataRank · unranked

0 citations

Karen N. McFarland, Jennifer B. Phillips, Mariet Allen, Christian Lessard, Lillian Zobel +12 more

Affinity purification of in vivo assembled whirlin-associated protein complexes from the zebrafish retina

Journal of Proteomics(2022)10.1016/j.jprot.2022.104666

N/A

0DataRank · unranked

2 citations

Ralph Slijkerman, Lisette Hetterschijt, Theo Peters, Sanne Broekman, Aurélie Clément +7 more