Cesar Alves

Also affiliated with Children's Hospital of Philadelphia, Harvard University, Great Ormond Street Hospital, 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 17 papers. Top paper: “Central Dysmyelination in SSADH‐Deficient Humans and Mice”.

Central Dysmyelination in SSADH‐Deficient Humans and Mice

Annals of Clinical and Translational Neurology(2025)10.1002/acn3.70148

N/A

0.104DataRank · unranked

1 citations

Henry H.C. Lee, Edward Yang, Cesar Alves, Mariarita Bertoldi, Caitlyn Fung +7 more

Imaging Patterns Characterizing Mitochondrial Leukodystrophies

American Journal of Neuroradiology(2021)10.3174/ajnr.a7097

N/A

0DataRank · unranked

60 citations

Tim van de Brug, Cesar Alves, Susan Blasér, Adeline Vanderver, Nicole I. Wolf +2 more

Correction to: Genetic and Clinical Predictors of Ataxia in Pediatric Primary Mitochondrial Disorders

The Cerebellum(2022)10.1007/s12311-022-01370-y

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0DataRank · unranked

0 citations

Sara Reis Teixeira, Cesar Alves, Fabrício Guimarães Gonçalves, Luis Octavio Tierradentro‐García, Martin Kidd +4 more

Loss of symmetric cell division of apical neural progenitors drives DENND5A -related developmental and epileptic encephalopathy

medRxiv(2022)10.1101/2022.08.23.22278845

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0DataRank · unranked

0 citations

Vincent Francis, Sheng‐Jia Lin, Fares Kharfallah, Vladimir S. Fonov, Maxime Levesque +80 more

Heterozygous nonsense variants in the ferritin heavy-chain gene FTH1 cause a neuroferritinopathy

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100236

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0DataRank · unranked

17 citations

Jesus A Tintos-Hernández, Chaya N. Murali, Monica Penon‐Portmann, Marco Flores‐Méndez, Adrian Santana +12 more

Expansion of clinical and variant spectrum of EEF2‐related neurodevelopmental disorder: Report of two additional cases

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63230

N/A

0DataRank · unranked

4 citations

Alyssa L. Rippert, Edward Cook, Cesar Alves, Lynne M. Bird, Kosuke Izumi +1 more

Heterozygous Nonsense Variants in the Ferritin Heavy Chain Gene FTH1 Cause a Novel Pediatric Neuroferritinopathy

medRxiv(2023)10.1101/2023.01.30.23285099

N/A

0DataRank · unranked

1 citations

Jesus A Tintos-Hernández, Chaya N. Murali, Monica Penon‐Portmann, Marco Flores‐Méndez, Adrian Santana +12 more

Clinical and neuroradiological spectrum of biallelic variants in NOTCH3

EBioMedicine(2024)10.1016/j.ebiom.2024.105297

N/A

0DataRank · unranked

12 citations

Cesar Alves, Aisha M. Al Shamsi, Gehad ElGhazali, Maha S. Zaki, Lorenzo Pinelli +46 more

Involvement of the Spinal Cord in Primary Mitochondrial Disorders: A Neuroimaging Mimicker of Inflammation and Ischemia in Children

American Journal of Neuroradiology(2020)10.3174/ajnr.a6910

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0DataRank · unranked

14 citations

Amy Goldstein, Sara Reis Teixeira, Juan Sebastián Martín-Saavedra, Isabella Peixoto de Barcelos, Giulia Fadda +9 more

Biallelic variants in GTF3C3 encoding a subunit of the TFIIIC2 complex are associated with neurodevelopmental phenotypes in humans and zebrafish

Brain Communications(2024)10.1093/braincomms/fcaf055

N/A

0DataRank · unranked

3 citations

Adeline Paimboeuf, Maha S. Zaki, Fernanda Barbosa Figueiredo, Sherif F. Abdel‐Ghafar, Sabrina Maher +12 more

Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy

Nature Communications(2024)10.1038/s41467-024-51310-z

N/A

0DataRank · unranked

5 citations

Vincent Francis, Sheng‐Jia Lin, Fares Kharfallah, Vladimir S. Fonov, Maxime Lévesque +80 more

Biallelic variants in GTF3C5, a regulator of RNA polymerase III-mediated transcription, cause a multisystem developmental disorder

Human Genetics(2024)10.1007/s00439-024-02656-3

N/A

0DataRank · unranked

2 citations

Cara Skraban, Atsunori Yoshimura, Toyonori Sakata, Cesar Alves, Sarah K. Fiordaliso +16 more

An inappropriate decline in ribosome levels drives a diverse set of neurodevelopmental disorders

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.01.09.574708

N/A

0DataRank · unranked

3 citations

Leqian Yu, Barbara Vona, Dayea Park, Yulei Wei, Daniel A. Schmitz +30 more

MAPK signaling and angiopoietin-2 contribute to endothelial permeability in capillary malformations

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2509528122

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0DataRank · unranked

5 citations

Mariam Baig, Jill Wylie‐Sears, Matthew P. Vivero, Patrick Smits, Annegret Holm +7 more

ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy

Genetics in Medicine(2025)10.1016/j.gim.2025.101506

N/A

0DataRank · unranked

3 citations

Chu-Ting Chang, A. Declève, Gloria Brunori, W.H. Ludlam, Alden Huang +93 more

Variable Flip Angle Optimization for Fetal Brain Imaging With Reduced Specific Absorption Rate

NMR in Biomedicine(2025)10.1002/nbm.70075

N/A

0DataRank · unranked

2 citations

Camilo Calixto, Hongli Fan, Camilo Jaimes, Clemente Velasco‐Annis, Suely Fazio Ferraciolli +5 more

Bi-allelic MYMX variants cause a syndromic congenital myopathy with recognizable facial palsy, growth restriction, and dysmorphism

European Journal of Human Genetics(2024)10.1038/s41431-024-01759-9

N/A

0DataRank · unranked

3 citations

Luisa Marsili, Domizia Pasquetti, Abolfazl Rad, Muhammad Nadeem Anjum, Gabriela Oprea +9 more