Miriam H. Meisler

Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicine

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 11 papers. Top paper: “Scn8a Antisense Oligonucleotide Is Protective in Mouse Models of SCN8A Encephalopathy and Dravet Syndrome”.

Scn8a Antisense Oligonucleotide Is Protective in Mouse Models of SCN8A Encephalopathy and Dravet Syndrome

Annals of Neurology(2020)10.1002/ana.25676

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0DataRank · unranked

141 citations

Paymaan Jafar‐Nejad, Sophie F. Hill, Lucas D. Huffman, Corrine Smolen, Jacy L. Wagnon +9 more

Gabra2 is a genetic modifier of Scn8a encephalopathy in the mouse*

Epilepsia(2020)10.1111/epi.16741

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0DataRank · unranked

20 citations

Sophie F. Hill, James G. Xenakis, Fernando Pardo‐Manuel de Villena, Jacy L. Wagnon, Miriam H. Meisler +1 more

Postictal Death Is Associated with Tonic Phase Apnea in a Mouse Model of Sudden Unexpected Death in Epilepsy

Annals of Neurology(2021)10.1002/ana.26053

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57 citations

Frida A. Teran, Eric R. Wengert, Pravin K. Wagley, Payal S. Panchal, Elizabeth A. Blizzard +7 more

Correction of the hypomorphic Gabra2 splice site variant in mouse strain C57BL/6J modifies the severity of Scn8a encephalopathy

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100064

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5 citations

Megan K. Mulligan, Robert W. Williams, Miriam H. Meisler, Wenxi Yu

Genetic interaction between Scn8a and potassium channel genes Kcna1 and Kcnq2

Epilepsia(2022)10.1111/epi.17374

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0DataRank · unranked

19 citations

Julie Ziobro, Paymaan Jafar‐Nejad, Frank Rigo, Miriam H. Meisler, Sophie F. Hill

Chloroquine corrects enlarged lysosomes in FIG4 null cells and reduces neurodegeneration in Fig4 null mice

Molecular Genetics and Metabolism(2022)10.1016/j.ymgme.2022.11.004

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8 citations

Miriam H. Meisler, Guy M. Lenk

The chloride antiporter CLCN7 is a modifier of lysosome dysfunction in FIG4 and VAC14 mutants

PLoS Genetics(2023)10.1371/journal.pgen.1010800

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0DataRank · unranked

16 citations

Guy M. Lenk, Vedrana Mikušević, Joseph A. Mindell, Miriam H. Meisler, Xu Cao

Altered phenotypes due to genetic interaction between the mouse phosphoinositide biosynthesis genes Fig4 and Pip4k2c

G3 Genes Genomes Genetics(2023)10.1093/g3journal/jkad007

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0DataRank · unranked

5 citations

Guy M. Lenk, Miriam H. Meisler, Xu Cao

Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101097

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0DataRank · unranked

10 citations

Young Nyun Park, Guy M. Lenk, Mariasavina Severino, Marcello Scala, Jonas Denecke +17 more

Dentate gyrus granule cells are a locus of pathology in Scn8a developmental encephalopathy

Neurobiology of Disease(2024)10.1016/j.nbd.2024.106591

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6 citations

Sophie F. Hill, Limei Zhu, Yiannos Demetriou, Faith Reger, Joanna Mattis +2 more

Protein family FAM241 in human and mouse

Mammalian Genome(2024)10.1007/s00335-024-10096-7

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1 citations

Young Nyun Park, Daniel G. Calame, Jacob O. Kitzman, Guy M. Lenk, Miriam H. Meisler +1 more