Kshitij Mankad

Also affiliated with Great Ormond Street Hospital for Children NHS Foundation Trust, University College London

Medicine

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 18 papers. Top paper: “Pediatric MOG-Ab–Associated Encephalitis”.

Pediatric MOG-Ab–Associated Encephalitis

Neurology Neuroimmunology & Neuroinflammation(2024)10.1212/nxi.0000000000200323

N/A

0.449DataRank · unranked

19 citations

Dimitrios Champsas, Michael Eyre, Omar Abdel‐Mannan, Vanessa Wan Mun Lee, Alison Skippen +18 more

The Cardiofaciocutaneous Syndrome: From Genetics to Prognostic–Therapeutic Implications

Genes(2023)10.3390/genes14122111

N/A

0.449DataRank · unranked

19 citations

Emanuele David, Elisa Calì, Roberto Chimenz, Saverio La Bella, Armando Di Ludovico +8 more

Spatiotemporal changes in along-tract profilometry of cerebellar peduncles in cerebellar mutism syndrome

NeuroImage Clinical(2022)10.1016/j.nicl.2022.103000

N/A

0.396DataRank · unranked

13 citations

Lisa Bruckert, Rashad Jabarkheel, Derek Yecies, Michael Zhang, Chris Clark +7 more

Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.015

N/A

0.312DataRank · unranked

7 citations

Cailyn P Leo, Chenghong Deng, Sheng‐Jia Lin, Reza Maroofian, Reneé C. Lin +95 more

Birth-related subdural hemorrhage in asymptomatic neonates: evolution over time and differentiation from traumatic subdural hemorrhage

Pediatric Radiology(2024)10.1007/s00247-024-06003-6

N/A

0.292DataRank · unranked

6 citations

Sriram Jaganathan, Arabinda K. Choudhary, Xiawei Ou, Rhea Choudhary, Anya Choudhary +5 more

MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia

Movement Disorders(2022)10.1002/mds.29147

N/A

0DataRank · unranked

11 citations

Robert Spaull, Smrithi Salian, Katy Barwick, Esther Meyer, Juan Zhen +32 more

Clinical Phenotype in Individuals With Birk-Landau-Perez Syndrome Associated With Biallelic SLC30A9 Pathogenic Variants

Neurology(2023)10.1212/wnl.0000000000207241

N/A

0DataRank · unranked

3 citations

Federica Rachele Danti, Mohamed Abunada, Benjamin Kamien, Sony Malhotra, Maya Topf +11 more

An international study presenting a federated learning AI platform for pediatric brain tumors

Nature Communications(2024)10.1038/s41467-024-51172-5

N/A

0DataRank · unranked

40 citations

Michelle Han, Jason L. Wright, Michael Kuwabara, Jacob Mevorach, Gang Fu +39 more

2021 MAGNIMS–CMSC–NAIMS consensus recommendations on the use of MRI in patients with multiple sclerosis

The Lancet Neurology(2021)10.1016/s1474-4422(21)00095-8

N/A

0DataRank · unranked

650 citations

Olga Ciccarelli, Daniel S. Reich, Brenda Banwell, Nicola De Stefano, Christian Enzinger +21 more

Automated and Interpretable Detection of Hippocampal Sclerosis in Temporal Lobe Epilepsy: AID ‐ HS

Annals of Neurology(2024)10.1002/ana.27089

N/A

0DataRank · unranked

11 citations

Jordan DeKraker, Maria H. Eriksson, Rory J. Piper, Siby Gopinath, Harilal Parasuram +40 more

Human mutations in SLITRK3 implicated in GABAergic synapse development in mice

Frontiers in Molecular Neuroscience(2024)10.3389/fnmol.2024.1222935

N/A

0DataRank · unranked

5 citations

Wenyan Han, Muhammad Ilyas, Jun Li, Yichao Yu, Marcello Scala +22 more

Biallelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a syndromic neurodevelopmental disorder

medRxiv(2024)10.1101/2024.07.18.24310581

N/A

0DataRank · unranked

1 citations

Cailyn P Leo, Chenghong Deng, Kejia Zhang, Sheng‐Jia Lin, Reza Maroofian +75 more

Slowly Expanding Lesions in Pediatric-Onset Multiple Sclerosis

JAMA Neurology(2025)10.1001/jamaneurol.2025.2619

N/A

0DataRank · unranked

5 citations

Ferrán Prados, N.-Y. Kim, Omar Abdel‐Mannan, Riccardo Nistri, Philipp Goebl +16 more

Radiologic Lag and Brain MRI Lesion Dynamics During Attacks in MOG Antibody–Associated Disease

Neurology(2024)10.1212/wnl.0000000000209303

N/A

0DataRank · unranked

43 citations

Omar Abdel‐Mannan, Dimitrios Champsas, Kshitij Mankad, Karl N. Krecke, John J. Chen +11 more

Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.003

N/A

0DataRank · unranked

34 citations

Stéphanie Efthymiou, Simone Seiffert, Karen Vargas Parra, Sukyeong Lee, Alessia Nasca +35 more

Radiomic signatures of posterior fossa ependymoma: Molecular subgroups and risk profiles

Neuro-Oncology(2021)10.1093/neuonc/noab272

N/A

0DataRank · unranked

24 citations

Edward Wang, Derek Yecies, Lydia Tam, Michelle Han, Sebastian Toescu +25 more

Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study

Brain(2022)10.1093/brain/awac224

N/A

0DataRank · unranked

135 citations

Mathilde Ripart, Kirstie Whitaker, Felice D’Arco, Kshitij Mankad, Andrew A. Chen +72 more

MRI Radiogenomics of Pediatric Medulloblastoma: A Multicenter Study

Radiology(2022)10.1148/radiol.212137

N/A

0DataRank · unranked

75 citations

Samuel W Wong, Jason N. Wright, Matthias Wagner, Sebastian Toescu, Michelle Han +34 more