Manju A. Kurian

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

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 21 papers. Top paper: “NovelDNM1Lvariants impair mitochondrial dynamics through divergent mechanisms”.

NovelDNM1Lvariants impair mitochondrial dynamics through divergent mechanisms

Life Science Alliance(2022)10.26508/lsa.202101284

N/A

0.871DataRank · unranked

25 citations

John M. Egner, Jack J. Collier, Oliver M. Russell, Charlotte L. Alston, Megan Cleland Harwig +19 more

Evolution of Movement Disorders in Patients With CLN2-Batten Disease Treated With Enzyme Replacement Therapy

Neurology(2024)10.1212/wnl.0000000000209615

N/A

0.330DataRank · unranked

8 citations

Audrey Soo, Spyros Batzios, Emma Footitt, Rebecca Whiteley, Jonathan W. Mink +4 more

Genetic therapies for neurological diseases

Pharmacological Reviews(2025)10.1016/j.pharmr.2025.100093

N/A

0.208DataRank · unranked

3 citations

Manju A. Kurian, Haiyan Zhou, Ross Ferguson, Sarah J. Tabrizi, Gabriele Lignani +3 more

Cardiac glycosides restore autophagy flux in an iPSC-derived neuronal model of WDR45 deficiency

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.13.556416

N/A

0.208DataRank · unranked

3 citations

Nivedita Singh, Lorita Gianfrancesco, Dimitri Budinger, Katy Barwick, Alexander Agrotis +13 more

The dopamine transporter gene SLC6A3: multidisease risks

Molecular Psychiatry(2021)10.1038/s41380-021-01341-5

N/A

0DataRank · unranked

108 citations

Sandhya Kortagere, Corinde E. Wiers, Hui Sun, Manju A. Kurian, Aurelio Galli +3 more

Consensus clinical management guideline for beta‐propeller protein‐associated neurodegeneration

Developmental Medicine & Child Neurology(2021)10.1111/dmcn.14980

N/A

0DataRank · unranked

50 citations

Allison Gregory, Manju A. Kurian, Ittai Bushlin, Fanny Mochel, Lisa Emrick +5 more

TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.019

N/A

0DataRank · unranked

47 citations

Heidi Cope, Zelha Nil, Thomas A. Ravenscroft, Wu‐Lin Charng, Shenzhao Lu +42 more

Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia

Journal of Clinical Investigation(2021)10.1172/jci140625

N/A

0DataRank · unranked

39 citations

Marisa M. Brockmann, Jinye Dai, Sander Pajusalu, Burcu Atasu, Joaquín Campos +30 more

Psychomotor impairments and therapeutic implications revealed by a mutation associated with infantile Parkinsonism-Dystonia

eLife(2021)10.7554/elife.68039

N/A

0DataRank · unranked

23 citations

Mary Hongying Cheng, Josep Font, Alexandra C. Schwartz, Kaitlyn V. Ledwitch, Amanda M. Duran +14 more

Psychomotor Impairments and Therapeutic Implications Revealed by a Mutation Associated with Infantile Parkinsonism-Dystonia

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.09.434693

N/A

0DataRank · unranked

0 citations

Mary Hongying Cheng, Josep Font, Alexandra C. Schwartz, Kaitlyn V. Ledwitch, Amanda M. Duran +14 more

Gain-of-function GABRB3 variants identified in vigabatrin-hypersensitive epileptic encephalopathies

Brain Communications(2020)10.1093/braincomms/fcaa162

N/A

0DataRank · unranked

35 citations

Vivian W. Y. Liao, Kavitha Kothur, Dinesh C. Indurthi, Bruce Bennetts, Christopher Troedson +16 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

Bi-allelic variants in INTS11 are associated with a complex neurological disorder

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.012

N/A

0DataRank · unranked

38 citations

Erica L. Macke, Marcello Niceta, Monika Weisz Hubshman, Oguz Kanca, Laura Schultz‐Rogers +95 more

Fetal gene therapy

Journal of Inherited Metabolic Disease(2023)10.1002/jimd.12659

N/A

0DataRank · unranked

28 citations

William H. Peranteau, Ahad A. Rahim, Ashley K. Boyle, Manju A. Kurian, Paul Gissen +3 more

Transitional Care for Young People with Movement Disorders: Consensus‐Based Recommendations from the MDS Task Force on Pediatrics

Movement Disorders Clinical Practice(2023)10.1002/mdc3.13728

N/A

0DataRank · unranked

10 citations

Amit Batla, Ali Shalash, Jitendra Kumar Sahu, Carlos Cosentino, Darius Ebrahimi‐Fakhari +18 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

Co-occurring WARS2 and CHRNA6 mutations in a child with a severe form of infantile parkinsonism

Parkinsonism & Related Disorders(2020)10.1016/j.parkreldis.2020.02.003

N/A

0DataRank · unranked

21 citations

Viviana Cordeddu, Serena Galosi, Ambra Lanzo, Eleonora Palma, Luca Pannone +28 more

Mouse models for inherited monoamine neurotransmitter disorders

Journal of Inherited Metabolic Disease(2024)10.1002/jimd.12710

N/A

0DataRank · unranked

7 citations

Joanne Ng, Manju A. Kurian, Philippa B. Mills, Aurora Martı́nez, Beat Thöny

De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy

Genetics in Medicine(2020)10.1038/s41436-020-01020-w

N/A

0DataRank · unranked

47 citations

Heinrich Sticht, Pia Zacher, Bernt Popp, Holly E. Babcock, Dewi P. Bakker +53 more

Hyperkinetic Movement Disorder Caused by the Recurrent c. 892C >T NACC1 Variant

Movement Disorders Clinical Practice(2024)10.1002/mdc3.14051

N/A

0DataRank · unranked

4 citations

Salla M. Kangas, Estrella López‐Martín, Timothy Feyma, Fernando Scaglia, Beatriz Martínez–Delgado +7 more

Psychiatric comorbidity is common in dystonia and other movement disorders

Archives of Disease in Childhood(2020)10.1136/archdischild-2020-319541

N/A

0DataRank · unranked

5 citations

Isobel Heyman, Benjamin Baig, Anna Coughtrey, Andrew McWilliams, David Dossetor +13 more