Mia MacCollin - Concepedia

Author

Mia MacCollin

Also Known As

James Gusella, M M MacCollin, M MacCollin, M. M. MacCollin, M. MaCcollin, M. MacCollin, MIA MACCOLLIN, Mia M. MacCollin, Mia M. Maccollin, Mia MacCollin

Publications

6.1K

Citations

H-Index

Concepts

All Affiliations

Massachusetts General Hospital Harvard University Universität Hamburg University Medical Center Hamburg-Eppendorf Brigham and Women's Hospital

About

Mia MacCollin is an author at Massachusetts General Hospital specializing in medicine, cell biology, and neuro-oncology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	25	2.6K
2	Education	1	1	61
3	Health Sciences	1	1	61
4	Natural Sciences	1	1	420
5	Social Sciences	1	1	51

Mia MacCollin

Publications

4.9K

Citations

H-Index

Page 1

	Year	Citations
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation Eric Legius, Ludwine Messiaen, P. Wolkenstein, Genetics in Medicine	2021	687
A negative feedback signaling network underlies oncogene-induced senescence Stéphanie Courtois-Cox, Sybil M. Genther Williams, Elizabeth E. Reczek, Cancer Cell Signal TransductionCellular SenescenceNegative FeedbackSystems BiologyMedicine	2006	482
Random-clone strategy for genomic restriction mapping in yeast. Maynard V. Olson, James E. Dutchik, Monica Graham, Proceedings of the National Academy of Sciences Comparative GenomicsGeneticsMolecular GeneticsGenomicsYeast Dna	1986	420
Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. Martin Ruttledge, Anne Andermann, Catherine M. Phelan, PubMed	1996	259
Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation Scott R. Plotkin, Ludwine Messiaen, Eric Legius, Genetics in Medicine	2022	247
Survey of Somatic Mutations in Tuberous Sclerosis Complex (TSC) Hamartomas Suggests Different Genetic Mechanisms for Pathogenesis of TSC Lesions Yo Niida, Anat Stemmer‐Rachamimov, Marian L. Logrip, The American Journal of Human Genetics Tuberous Sclerosis ComplexDevelopmental AnomalySomatic VariantSomatic MutationsGenetic Disorder	2001	201
Molecular Analysis of the NF2 Tumor-Suppressor Gene in Schwannomatosis Lee B. Jacoby, Deborah Jones, Kevin Davis, The American Journal of Human Genetics Neuro-oncologyPathologyTumor SuppressorCancer GeneticsMedicine	1997	183
Frequency and distribution ofNF2 mutations in schwannomas Lee B. Jacoby, Mia MacCollin, Rosemary Barone, Genes Chromosomes and Cancer	1996	157
Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1) David H. Gutmann, Sonja A. Rasmussen, P. Wolkenstein, Neurology Neuro-oncologyPediatric Brain TumorsNeurofibromatosis 1Age 10Brain Tumor Biology	2002	154
Alterations in the <i>SMARCB1 </i>(<i>INI1</i>) tumor suppressor gene in familial schwannomatosis C. D. Boyd, Lan Kluwe, A. Balogh, Clinical Genetics Neuro-oncologySomatic VariantMedicineGeneticsTumor Suppressor Gene	2008	152

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