Chong Ae Kim - Concepedia

Author

Chong Ae Kim

Also Known As

A Yushchenko, A. Kim Chong, Ae Kim Chong, Alexsandra Malaquias, C A E Kim, C A Kim, C Kim, C. A. Kim, C. Ae Kim, C. E. A. Kim

538

Publications

19.4K

Citations

H-Index

254

Concepts

All Affiliations

Universidade de São Paulo Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo Universidade Federal de São Paulo Hospital de Clínicas de Porto Alegre Universidade Federal do Rio Grande do Sul

About

Chong Ae Kim is an author at Universidade de São Paulo specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	40	81	7.9K
2	Health Sciences	6	6	239
3	Education	2	2	56
4	Engineering	1	1	75
5	Management	1	1	35

Chong Ae Kim

186

Publications

13.7K

Citations

H-Index

Page 1

	Year	Citations
LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development Yaoqin Gong, Roger B. Slee, N Fukai, Cell Bone AccrualSclerostinSignal TransductionMolecular PhysiologyDevelopmental Biology	2001	2.2K
Role of βγ Subunits of G Proteins in Targeting the β-Adrenergic Receptor Kinase to Membrane-Bound Receptors Julie A. Pitcher, James Inglese, Joyce B. Higgins, Science	1992	715
Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans Stephen P. Robertson, Stephen R.F. Twigg, Andrew J. Sutherland‐Smith, Nature Genetics Developmental BiologyMendelian DisorderGenetic DisorderCytoskeletal ProteinGenetics	2003	426
Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy Chong Ae Kim, Marc Délepine, Emilie Boutet, The Journal of Clinical Endocrinology & Metabolism	2008	386
Mutations in the Transmembrane Natriuretic Peptide Receptor NPR-B Impair Skeletal Growth and Cause Acromesomelic Dysplasia, Type Maroteaux Cynthia F. Bartels, Hülya Bükülmez, Pius S. Padayatti, The American Journal of Human Genetics SclerostinSignal TransductionMolecular PhysiologyBone Morphogenic ProteinGenetic Disorder	2004	363
Serum leptin level is a regulator of bone mass Florent Elefteriou, S. Takeda, Ken Ebihara, Proceedings of the National Academy of Sciences	2004	332
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome José Roberto Marcelino, John D. Carpten, Wafaa M. Suwairi, Nature Genetics CardiomyopathyCamptodactyly-arthropathy-coxa Vara-pericarditis SyndromeMedicinePathogenesisImmunology	1999	322
Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss Michael A. Simpson, Melita Irving, Esra Asilmaz, Nature Genetics Progressive Bone LossCraniofacial DisorderGenetic DisorderHematologyPathology	2011	306
Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis Deborah Krakow, Stephen P. Robertson, Lily King, Nature Genetics Developmental BiologyBone Morphogenic ProteinGenetic DisorderGeneticsCraniofacial Development	2004	287
Congenital abnormalities in Brazilian children associated with misoprostol misuse in first trimester of pregnancy Claudette Hajaj Gonzalez, Maria Joaquina Marques‐Dias, Chong Ae Kim, The Lancet First TrimesterAbortionMiscarriage TestingPediatricsGynecology	1998	273

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