Kyle P. Flannery

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 7 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

0DataRank · unranked

11 citations

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

N/A

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

N/A

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