Jeong‐In Baek - Concepedia

Author

Jeong‐In Baek

Kyungpook National University

Also Known As

J.‐I. Baek, Jae Yeon Lee, Jeong-In Baek, Jeong‐In Baek

Publications

Citations

H-Index

Concepts

All Affiliations

Kyungpook National University Daegu Haany University Yonsei University University of Pennsylvania Ralph H. Johnson VA Medical Center

About

Jeong‐In Baek is an author at Kyungpook National University specializing in medicine, genetics, and hearing loss.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	13	393
2	Arts	7	7	185
3	Engineering	3	3	147
4	Natural Sciences	2	2	46
5	Health Sciences	1	1	13

Jeong‐In Baek

Publications

969

Citations

H-Index

Page 1

	Year	Citations
Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families Jeong‐In Baek, Se‐Kyung Oh, Kim Dong-Bin, Orphanet Journal of Rare Diseases	2012	94
Effective PEI-mediated delivery of CRISPR-Cas9 complex for targeted gene therapy Nari Ryu, Min-A Kim, Dongsik Park, Nanomedicine Nanotechnology Biology and Medicine Gene TherapiesEngineeringMolecular BiologyGenetic EngineeringGene Editing	2018	93
Evaluating protective and therapeutic effects of alpha-lipoic acid on cisplatin-induced ototoxicity Kyung‐Hee Kim, Byeonghyeon Lee, Ye‐Ri Kim, Cell Death and Disease	2018	67
Therapeutic potential of the mitochondria-targeted antioxidant MitoQ in mitochondrial-ROS induced sensorineural hearing loss caused by Idh2 deficiency Ye‐Ri Kim, Jeong‐In Baek, Sung Hwan Kim, Redox Biology	2018	60
Identification of Pathogenic Mechanisms of<i>COCH</i>Mutations, Abolished Cochlin Secretion, and Intracellular Aggregate Formation: Genotype-Phenotype Correlations in DFNA9 Deafness and Vestibular Disorder Seung-Hyun Bae, Nahid G. Robertson, Hyun-Ju Cho, Human Mutation	2014	54
Evidence for a founder mutation causing DFNA5 hearing loss in East Asians Hong-Joon Park, Hyun-Ju Cho, Jeong‐In Baek, Journal of Human Genetics Founder MutationGenetic DisorderMedicineGeneticsAudiology	2009	49
Mutational Analysis of EYA1, SIX1 and SIX5 Genes and Strategies for Management of Hearing Loss in Patients with BOR/BO Syndrome Mee Hyun Song, Tae-Jun Kwon, Hui Ram Kim, PLoS ONE	2013	44
Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families Hae-Mi Woo, Hong-Joon Park, Jeong‐In Baek, BMC Medical Genetics	2013	39
A Post-Developmental Genetic Screen for Zebrafish Models of Inherited Liver Disease Seok-Hyung Kim, Shu-Yu Wu, Jeong‐In Baek, PLoS ONE EngineeringGeneticsGenetic EpidemiologyF2 LinesMolecular Genetics	2015	39
Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing loss. Borum Sagong, Raekil Park, Yee-Hyuk Kim, PubMed GeneticsMolecular BiologyMolecular GeneticsDisease Gene IdentificationMendelian Disorder	2010	36

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