M. Chiara Manzini

Rutgers, The State University of New Jersey

ChemistryBiochemistry, 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 17 papers. Top paper: “Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a severe developmental disorder spectrum”.

Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a severe developmental disorder spectrum

Genetics in Medicine(2024)10.1016/j.gim.2024.101273

N/A

0.373DataRank · unranked

11 citations

Jovi Huixin Wong, Puravi Panda, Dat Nguyen, Nancy C.P. Leong, Riccardo Sangermano +62 more

Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophy

Molecular Genetics & Genomic Medicine(2020)10.1002/mgg3.1387

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0DataRank · unranked

4 citations

Alan Pittman, Swati Mummidivarpu, Ehsan Ghayoor Karimiani, Samantha Martinez, Isabella Moroni +7 more

Digging behavior discrimination test to probe burrowing and exploratory digging in male and female mice

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.29.424478

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0DataRank · unranked

1 citations

Abigail T. Heller, Brian M. Gural, Olivia McKissick, Molly Wilkinson, M. Chiara Manzini +1 more

Digging behavior discrimination test to probe burrowing and exploratory digging in male and female mice

Journal of Neuroscience Research(2021)10.1002/jnr.24857

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0DataRank · unranked

38 citations

Abigail T. Heller, Brian M. Gural, Olivia McKissick, Molly Wilkinson, M. Chiara Manzini +1 more

Unraveling the mysteries of MYT1L: From reprogramming factor to multifaceted regulator of neuronal differentiation

Neuron(2021)10.1016/j.neuron.2021.11.006

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0DataRank · unranked

7 citations

M. Chiara Manzini, Aniket Bhattacharya

Cc2d1b Contributes to the Regulation of Developmental Myelination in the Central Nervous System

Frontiers in Molecular Neuroscience(2022)10.3389/fnmol.2022.881571

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0DataRank · unranked

10 citations

Jiayue Hong, Haley Jeanette, Simrandeep K Brar, Anish Yalamanchili, M. Laura Feltri +4 more

Duplicated zebrafish ( Danio rerio ) inositol phosphatases inpp5ka and inpp5kb diverged in expression pattern and function

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.08.31.506059

N/A

0DataRank · unranked

1 citations

Brian M. Gural, Edmund Cauley, Llion E. Roberts, Brittany F. Karas, Luca Cavallo +5 more

Duplicated zebrafish (Danio rerio) inositol phosphatases inpp5ka and inpp5kb diverged in expression pattern and function

Development Genes and Evolution(2023)10.1007/s00427-023-00703-z

N/A

0DataRank · unranked

2 citations

Brian M. Gural, Edmund Cauley, Namarata Battula, Shorbon Mowla, Brittany F. Karas +7 more

Standardization of zebrafish drug testing parameters for muscle diseases

Disease Models & Mechanisms(2024)10.1242/dmm.050339

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0DataRank · unranked

23 citations

Katherine G. English, Clarissa A. Henry, M. Chiara Manzini, John M. Parant, Melissa A. Wright +7 more

Removal of pomt1 in zebrafish leads to loss of α-dystroglycan glycosylation and dystroglycanopathy phenotypes

Human Molecular Genetics(2024)10.1093/hmg/ddae006

N/A

0DataRank · unranked

4 citations

Kristin R. Terez, Shorbon Mowla, Namarata Battula, Kyle P. Flannery, Brian M. Gural +4 more

Genetic blueprint of congenital muscular dystrophies with brain malformations in Egypt: A report of 11 families

Neurogenetics(2024)10.1007/s10048-024-00745-z

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0DataRank · unranked

4 citations

Kyle P. Flannery, Ahmed A. El Beheiry, Mohamed Mokhtar, Ebtesam Abdalla, M. Chiara Manzini +1 more

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes

Neurogenetics(2024)10.1007/s10048-024-00773-9

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0DataRank · unranked

4 citations

Sylvia Safwat, Eli Matsell, Namarata Battula, Ahlam A. Hamed, Inaam N. Mohamed +11 more

Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders

medRxiv(2024)10.1101/2024.02.09.24302464

N/A

0DataRank · unranked

2 citations

Jovi Huixin Wong, Puravi Panda, Dat Nguyen, Nancy C.P. Leong, Riccardo Sangermano +57 more

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2 -related disorders caused by missense changes

medRxiv(2024)10.1101/2024.05.15.24306843

N/A

0DataRank · unranked

0 citations

Sylvia Safwat, Eli Matsell, Namarata Battula, Ahlam A. Hamed, Inaam N. Mohamed +11 more

Impact of maternal compensation on developmental phenotypes in a zebrafish model of severe congenital muscular dystrophy

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.13.653769

N/A

0DataRank · unranked

0 citations

Shorbon Mowla, Namarata Battula, Liana R. Clark, Deze Liu, Cristiana Oliveira +7 more

Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features

European Journal of Human Genetics(2020)10.1038/s41431-020-0669-x

N/A

0DataRank · unranked

36 citations

Geok Lin Chua, Cheen Fei Chin, Hessa S. Alsaif, Artem Borovikov, Saima Riazuddin +25 more

Interactome Analysis of the CC2D1A Scaffold Reveals Novel Neuronal Interactions and a Postsynaptic Role

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.06.26.661826

N/A

0DataRank · unranked

0 citations

Aniket Bhattacharya, Haorong Li, Luka Turkalj, Shruthi Thiyagarajan, Emiko Suzuki +5 more