Udai Bhan Pandey

Also affiliated with University of Pittsburgh Medical Center

MedicineBiochemistry, 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 29 papers. Top paper: “Axon guidance genes modulate neurotoxicity of ALS-associated UBQLN2”.

Axon guidance genes modulate neurotoxicity of ALS-associated UBQLN2

eLife(2023)10.7554/elife.84382

N/A

0.610DataRank · unranked

18 citations

Kye D Nichols, Eric N. Anderson, Yining Liu, Nandini Ramesh, Weiyan Jia +6 more

Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder

Nature Communications(2021)10.1038/s41467-021-22627-w

N/A

0.598DataRank · unranked

53 citations

Deepa Rajan, Tyler R. Fortuna, Eric N. Anderson, Caroline Ward, Youngha Lee +65 more

HuD impairs neuromuscular junctions and induces apoptosis in human iPSC and Drosophila ALS models

Nature Communications(2024)10.1038/s41467-024-54004-8

N/A

0.329DataRank · unranked

6 citations

Michela Mochi, Darilang Mawrie, Valeria de Turris, Alessio Colantoni, Beatrice Borhy +9 more

Impairment of the mitochondrial one-carbon metabolism enzyme SHMT2 causes a novel brain and heart developmental syndrome

Acta Neuropathologica(2020)10.1007/s00401-020-02223-w

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0DataRank · unranked

46 citations

Edgard Verdura, Natalia Juliá‐Palacios, Eric N. Anderson, Leire Goicoechea, Laura Planas‐Serra +33 more

RNA dependent suppression of C9orf72 ALS/FTD associated neurodegeneration by Matrin-3

Acta Neuropathologica Communications(2020)10.1186/s40478-020-01060-y

N/A

0DataRank · unranked

26 citations

Elizabeth L. Daley, Amanda M. Gleixner, Jacob R. Mann, Sukhleen Kour, Darilang Mawrie +6 more

Optogenetic TDP-43 nucleation induces persistent insoluble species and progressive motor dysfunction in vivo

Neurobiology of Disease(2020)10.1016/j.nbd.2020.105078

N/A

0DataRank · unranked

25 citations

Tyler R. Fortuna, Jacob R. Mann, Amanda M. Gleixner, Nandini Ramesh, Noah J. Pyles +3 more

Huntingtin-mediated axonal transport requires arginine methylation by PRMT6

Cell Reports(2021)10.1016/j.celrep.2021.108980

N/A

0DataRank · unranked

39 citations

Chiara Scaramuzzino, Eric N. Anderson, Debasmita Tripathy, Ivó H. Hernández, Rogan A. Grant +13 more

Nup62 is recruited to pathological condensates and promotes TDP-43 insolubility in C9orf72 and sporadic ALS/FTLD.

Research Square(2021)10.21203/rs.3.rs-144654/v1

N/A

0DataRank · unranked

1 citations

Brandie Morris Verdone, Charlton G. Otte, Nandini Ramesh, Jenna R. Gale, Jocelyn C. Mauna +11 more

WNK kinases sense molecular crowding and rescue cell volume via phase separation

Cell(2022)10.1016/j.cell.2022.09.042

N/A

0DataRank · unranked

198 citations

Daniel J. Shiwarski, Shawn E. Griffiths, Rebecca T. Beacham, Logan Norrell, Daryl E. Morrison +18 more

NUP62 localizes to ALS/FTLD pathological assemblies and contributes to TDP-43 insolubility

Nature Communications(2022)10.1038/s41467-022-31098-6

N/A

0DataRank · unranked

72 citations

Brandie Morris Verdone, Charlton G. Otte, Eric N. Anderson, Nandini Ramesh, Olivia R. Shapiro +13 more

Skeletal Muscle Pathogenesis in Polyglutamine Diseases

Cells(2022)10.3390/cells11132105

N/A

0DataRank · unranked

4 citations

Emanuela Zuccaro, Udai Bhan Pandey, Jessica Rosati, Manuela Basso, Maria Pennuto +1 more

CLIP-Seq Analysis Enables the Design of Ribosomal RNA Bait Oligonucleotides That Protect Against C9ORF72 ALS/FTD-Associated Poly-GR Pathophysiology

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.30.522259

N/A

0DataRank · unranked

1 citations

Ivan R. Sasselli, Marco Boccitto, Andrew C. Fleming, Tyler R. Fortuna, Yichen Li +11 more

Axon guidance pathways modulate neurotoxicity of ALS-associated UBQLN2

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.10.31.514355

N/A

0DataRank · unranked

0 citations

Kye D Nichols, Eric N. Anderson, Yining Liu, Nandini Ramesh, Weiyan Jia +6 more

Loss of function of the ALS-associated NEK1 kinase disrupts microtubule homeostasis and nuclear import

Science Advances(2023)10.1126/sciadv.adi5548

N/A

0DataRank · unranked

39 citations

Elizabeth D. McKenna, Darilang Mawrie, Vasileios Papakis, Francesco Alessandrini, Eric N. Anderson +10 more

LSD1/PRMT6-targeting gene therapy to attenuate androgen receptor toxic gain-of-function ameliorates spinobulbar muscular atrophy phenotypes in flies and mice

Nature Communications(2023)10.1038/s41467-023-36186-9

N/A

0DataRank · unranked

26 citations

Angela Bonadiman, Roberta Andreotti, Emanuela Zuccaro, Davide Dalfovo, Caterina Marchioretti +20 more

Drosha-dependent microRNAs modulate FUS-mediated neurodegeneration in vivo

Nucleic Acids Research(2023)10.1093/nar/gkad774

N/A

0DataRank · unranked

11 citations

Tyler R. Fortuna, Eric N. Anderson, Darilang Mawrie, Jessica Bilstein, Ramakrishnan Sivasubramanian +6 more

Antagonistic effect of cyclin-dependent kinases and a calcium-dependent phosphatase on polyglutamine-expanded androgen receptor toxic gain of function

Science Advances(2023)10.1126/sciadv.ade1694

N/A

0DataRank · unranked

12 citations

Laura Tosatto, Emanuela Zuccaro, Eric N. Anderson, Antonella Falconieri, María José Polanco +17 more

SMN regulates GEMIN5 expression and acts as a modifier of GEMIN5-mediated neurodegeneration

Acta Neuropathologica(2023)10.1007/s00401-023-02607-8

N/A

0DataRank · unranked

11 citations

Sukhleen Kour, Anuradha Venkatakrishnan Chimata, Anixa Muiños-Bühl, Eric N. Anderson, C Nelson +9 more

HuD (ELAVL4) gain-of-function impairs neuromuscular junctions and induces apoptosis in in vitro and in vivo models of amyotrophic lateral sclerosis

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.08.22.554258

N/A

0DataRank · unranked

1 citations

Michela Mochi, Darilang Mawrie, Valeria de Turris, Alessio Colantoni, Beatrice Borhy +7 more

MATR3 pathogenic variants differentially impair its cryptic splicing repression function

FEBS Letters(2024)10.1002/1873-3468.14806

N/A

0DataRank · unranked

13 citations

Xiao Xiao Chen, Michelle Dias, Jhune Rizsan Santos, Sukhleen Kour, Justin You +10 more

Unique tau‐ and synuclein‐dependent metabolic reprogramming in neurons distinct from normal aging

Aging Cell(2024)10.1111/acel.14277

N/A

0DataRank · unranked

6 citations

Aidan Graham, Farazdaq Al hammood, Chris Garbark, Deepika Vasudevan, Udai Bhan Pandey +4 more

Mutations of GEMIN5 are associated with coenzyme Q10 deficiency: long-term follow-up after treatment

European Journal of Human Genetics(2024)10.1038/s41431-023-01526-2

N/A

0DataRank · unranked

10 citations

Natalia Juliá‐Palacios, Roser Urreizti, Ana Sánchez‐Cuesta, Daniel J.M. Fernández‐Ayala, Elena García-Díaz +21 more

Function and dysfunction of GEMIN5: understanding a novel neurodevelopmental disorder

Neural Regeneration Research(2024)10.4103/nrr.nrr-d-23-01614

N/A

0DataRank · unranked

4 citations

Udai Bhan Pandey, C Nelson

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.12.004

N/A

0DataRank · unranked

1 citations

Stephan Drukewitz, Sukhleen Kour, Anuradha Venkatakrishnan Chimata, Deepa S. Rajan, Senta Schönnagel +53 more

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder

medRxiv(2025)10.1101/2025.03.31.25324695

N/A

0DataRank · unranked

2 citations

Stephan Drukewitz, Sukhleen Kour, Anuradha Venkatakrishnan Chimata, Deepa Rajan, Senta Schönnagel +54 more

RNA-recognition motif in Matrin-3 mediates neurodegeneration through interaction with hnRNPM

Acta Neuropathologica Communications(2020)10.1186/s40478-020-01021-5

N/A

0DataRank · unranked

53 citations

Sukhleen Kour, Eric N. Anderson, Dhivyaa Rajasundaram, Udai Bhan Pandey, Nandini Ramesh

Bi-allelic variants in the ribosomal protein RPS6KC1 cause a complex neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.09.015

N/A

0DataRank · unranked

0 citations

María E. Rodríguez-Ruiz, Eric N. Anderson, Agustí Rodríguez‐Palmero, Valentina Vélez-Santamaría, Agatha Schlüter +41 more

Insulin-like growth factor 1 signaling in motor neuron and polyglutamine diseases: From molecular pathogenesis to therapeutic perspectives

Frontiers in Neuroendocrinology(2020)10.1016/j.yfrne.2020.100821

N/A

0DataRank · unranked

19 citations

Udai Bhan Pandey, María José Polanco, Maria Pennuto

Inactivation of Hippo and cJun-N-terminal Kinase (JNK) signaling mitigate FUS mediated neurodegeneration in vivo

Neurobiology of Disease(2020)10.1016/j.nbd.2020.104837

N/A

0DataRank · unranked

46 citations

Ankita Sarkar, Abijeet Singh Mehta, Nandini Ramesh, Prajakta Deshpande, Madhuri Kango‐Singh +3 more