Johanna M. Rommens - Concepedia

Author

Johanna M. Rommens

Also Known As

Cutting, Garry R., J M Rommens, J Rommens, J. M. Rommens, J. ROMMENS, J. Rommens, J.M. Rommens, JOHANNA M. ROMMENS, Johanna M Rommens, Johanna M. Rommens

201

Publications

44.9K

Citations

H-Index

142

Concepts

All Affiliations

Hospital for Sick Children University of Toronto SickKids Foundation Public Health Ontario Johns Hopkins University

About

Johanna M. Rommens is an author at Hospital for Sick Children specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	50	72	37.8K
2	Natural Sciences	23	25	15.4K
3	Public Health	3	3	4.4K
4	Engineering	2	2	51
5	Health Sciences	2	2	1.1K

Johanna M. Rommens

124

Publications

43.1K

Citations

H-Index

Page 1

	Year	Citations
Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA John R. Riordan, Johanna M. Rommens, Bat-Sheva Kerem, Science GeneticsMolecular BiologyPathologyGene CharacterizationMolecular Genetics	1989	7.4K
Identification of the Cystic Fibrosis Gene: Genetic Analysis Bat-Sheva Kerem, Johanna M. Rommens, Janet A. Buchanan, Science Cystic Fibrosis GeneMendelian DisorderPhenylalanine ResidueGenetic DisorderMedicine	1989	4.1K
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease Robin Sherrington, Yuh‐Jin Liang, Ekaterina Rogaeva, Nature Neurodegenerative DiseasesEarly-onset Familial AlzheimerAlzheimer's DiseaseGenetic DisorderGenetics	1995	4K
Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping Johanna M. Rommens, Michael C. Iannuzzi, Bat-Sheva Kerem, Science Genetic AnalysisChromatinCystic Fibrosis GeneMendelian DisorderGenetic Disorder	1989	3.2K
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene Robin Sherrington, Ekaterina Rogaeva, Georges Lévesque, Nature Disease HeterogeneityAlzheimer's DiseaseMendelian DisorderGenetic DisorderGenetics	1995	2.1K
The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene Peter C. Bull, Gordon R. Thomas, Johanna M. Rommens, Nature Genetics Wilson Disease GeneGeneticsPathogenesisMenkes GeneMedicine	1993	1.9K
Mutant presenilins of Alzheimer's disease increase production of 42-residue amyloid β-protein in both transfected cells and transgenic mice Martin Citron, David Westaway, Weiming Xia, Nature Medicine Neurodegenerative DiseasesAlzheimer's DiseaseMolecular NeuroscienceNatural SciencesDisease Increase Production	1997	1.3K
Bone progenitor dysfunction induces myelodysplasia and secondary leukaemia Marc H.G.P. Raaijmakers, Siddhartha Mukherjee, Shangqin Guo, Nature Bone Marrow FailureMedicineHematologyMyeloid NeoplasiaOsteoarthritis	2010	1.1K
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome Toshinobu Matsuura, James S. Sutcliffe, Ping Fang, Nature Genetics Mendelian DisorderGenetic DisorderAngelman SyndromeGeneticsNatural Sciences	1997	868
The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds Sean V. Tavtigian, Jacques Simard, Johanna M. Rommens, Nature Genetics ChromatinCytogeneticsGenetic DisorderGeneticsComplete Brca2 Gene	1996	844

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