Paul C. Marcogliese

Children's Hospital Research Institute of Manitoba

Also affiliated with University of Manitoba

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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 15 papers. Top paper: “De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment”.

De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment

Human Molecular Genetics(2020)10.1093/hmg/ddaa081

N/A

1.1DataRank · unranked

41 citations

Lauren C. Briere, Oguz Kanca, Paul C. Marcogliese, Melissa Walker, Frances A. High +13 more

Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms

Neuron(2020)10.1016/j.neuron.2020.02.021

N/A

0.767DataRank · unranked

165 citations

Michael F. Wangler, Paul C. Marcogliese, Ju-Yeon Jo, Thomas A. Ravenscroft, Zhongyuan Zuo +29 more

De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.001

N/A

0.574DataRank · unranked

45 citations

Xiao Mao, Hua Wang, Ye-Jin Park, Paul C. Marcogliese, Jill A. Rosenfeld +12 more

A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levels

Nature Metabolism(2023)10.1038/s42255-023-00873-0

N/A

0.500DataRank · unranked

27 citations

Oguz Kanca, Seul Kee Byeon, Paul C. Marcogliese, Zhongyuan Zuo, Rishi V. Shridharan +11 more

Mechanisms of IRF2BPL-related disorders and identification of a potential therapeutic strategy

Cell Reports(2022)10.1016/j.celrep.2022.111751

N/A

0.434DataRank · unranked

17 citations

Debdeep Dutta, Cassandra N. Dennys, Samantha K. Powers, Florence Roussel, Paweł Lisowski +12 more

Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2322582121

N/A

0.292DataRank · unranked

6 citations

Oguz Kanca, Rishi V. Shridharan, Paul C. Marcogliese, Benjamin Steger, Marie Morimoto +92 more

Neuronal ROS-Induced Glial Lipid Droplet Formation is Altered by Loss of Alzheimer’s Disease-associated Genes

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.03.433580

N/A

0DataRank · unranked

13 citations

Scott Barish, Isha Ralhan, Jinlan Chang, Lindsey D. Goodman, Jake G. Harland +5 more

Drosophila functional screening of de novo variants in autism uncovers deleterious variants and facilitates discovery of rare neurodevelopmental diseases

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2020.12.30.424813

N/A

0DataRank · unranked

3 citations

Samantha L. Deal, Jonathan C. Andrews, J. Michael Harnish, Venkata Hemanjani Bhavana, Hillary K. Graves +39 more

Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases

Cell Reports(2022)10.1016/j.celrep.2022.110517

N/A

0DataRank · unranked

52 citations

Samantha L. Deal, Jonathan C. Andrews, J. Michael Harnish, Venkata Hemanjani Bhavana, Hillary K. Graves +56 more

Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.01.020

N/A

0DataRank · unranked

39 citations

Rebecca Hernan, Paul C. Marcogliese, Yan Huang, Tracy S. Gertler, Meltem Akçaboy +13 more

De novo variants in EMC1 lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in Drosophila

Human Molecular Genetics(2022)10.1093/hmg/ddac053

N/A

0DataRank · unranked

17 citations

Patrick Rump, Di Lu, Megan R. Glassford, Jung-Wan Mok, Jawid M. Fatih +12 more

TM2D genes regulate Notch signaling and neuronal function in Drosophila

PLoS Genetics(2021)10.1371/journal.pgen.1009962

N/A

0DataRank · unranked

11 citations

Sheng-An Yang, Yong Lin, David Li‐Kroeger, Paul C. Marcogliese, Samantha L. Deal +3 more

Neuronal ROS-induced glial lipid droplet formation is altered by loss of Alzheimer’s disease–associated genes

Proceedings of the National Academy of Sciences(2021)10.1073/pnas.2112095118

N/A

0DataRank · unranked

175 citations

Scott Barish, Isha Ralhan, Jinlan Chang, Lindsey D. Goodman, Jake G. Harland +5 more

Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in Drosophila

Nature Communications(2024)10.1038/s41467-024-47623-8

N/A

0DataRank · unranked

20 citations

Hyung-Lok Chung, Claire R. Y. Shih, Kenneth Kin Lam Wong, Debdeep Dutta, Zelha Nil +9 more

DrosophilaVoltage-Gated Sodium Channels Are Only Expressed in Active Neurons and Are Localized to Distal Axonal Initial Segment-like Domains

Journal of Neuroscience(2020)10.1523/jneurosci.0142-20.2020

N/A

0DataRank · unranked

76 citations

Jasper Janssens, Pei-Tseng Lee, Burak Tepe, Paul C. Marcogliese, Samira Makhzami +4 more