Alleene V. Strickland

Author

University of Miami

Also Known As

Alleene Strickland, Alleene V Strickland, Alleene V. Strickland

Publications

951

Citations

H-Index

Concepts

All Affiliations

University of Miami Dr. John T. Macdonald Foundation University of Antwerp VIB-UAntwerp Center for Molecular Neurology Anzac Research Institute

About

Alleene V. Strickland is an author at University of Miami specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	759
2	Public Health	2	2	268
3	Engineering	1	1	69
4	Biostatistics	1	1	19
5	Cell Biology	1	1	54

Alleene V. Strickland

Publications

951

Citations

H-Index

Page 1

	Year	Citations
Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success Vincent Timmerman, Alleene V. Strickland, Stephan Züchner Genes GeneticsGenetic EpidemiologyPathologyMolecular BiologyMolecular Genetics	2014	249
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder Alexander J. Abrams, Robert B. Hufnagel, Adriana Rebelo, Nature Genetics Somatic VariantMendelian DisorderGenetic DisorderGeneticsMolecular Biology	2015	200
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12 Gladys Montenegro, Adriana Rebelo, James W. Connell, Journal of Clinical Investigation Neurodegenerative DiseasesMendelian DisorderEr LocalizationHereditary Spastic ParaplegiasMedicine	2012	168
A novel mutation in VCP causes Charcot–Marie–Tooth Type 2 disease Michael Gonzalez, Shawna Feely, Fiorella Speziani, Brain	2014	138
Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1 Alleene V. Strickland, Maria Schabhüttl, H. Offenbacher, Journal of Neurology Genome InstabilityEngineeringSomatic VariantGenetic DisorderMedicine	2015	69
Characterization of the mitofusin 2 <scp>R94W</scp> mutation in a knock‐in mouse model Alleene V. Strickland, Adriana Rebelo, Fan Zhang, Journal of the Peripheral Nervous System MitophagyMitochondrial DysfunctionGeneticsMolecular BiologyCell Death	2014	54
<i>De novo PMP2</i>mutations in families with type 1 Charcot–Marie–Tooth disease William W. Motley, Paulius Palaima, Sabrina W. Yum, Brain	2016	43
Variant pathogenicity evaluation in the community-driven Inherited Neuropathy Variant Browser Cima Saghira, Dana M. Bis‐Brewer, David Staněk, Human Mutation GeneticsGenetic EpidemiologyPathologyDisease Gene IdentificationGenomics	2018	19
Characterizing the molecular phenotype of an Atp7a<sup>T985I</sup>conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX) Gonzalo Pérez‐Siles, Adrienne Grant, Melina Ellis, Metallomics	2016	11

Page 1