Lingling Ho - Concepedia

Author

Lingling Ho

University of Wisconsin–Madison

Also Known As

Lingling Ho

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

University of Wisconsin–Madison Hospital for Sick Children NYU Langone Health Oregon Health & Science University Juntendo University

About

Lingling Ho is an author at University of Wisconsin–Madison specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	787
2	Cell Biology	3	3	428
3	Health Sciences	1	1	253
4	Social Sciences	1	1	12
5	Biochemistry	1	1	85

Lingling Ho

Publications

Citations

H-Index

Page 1

	Year	Citations
Positional cloning of a gene for Hermansky–Pudlak syndrome, a disorder of cytoplasmic organelles Jangsuk Oh, Bailin Tu, Kazuyoshi Fukai, Nature Genetics ChromatinDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	1996	281
Retromer deficiency observed in Alzheimer's disease causes hippocampal dysfunction, neurodegeneration, and Aβ accumulation Alim Muhammad, Ingrid Flores, Hong Zhang, Proceedings of the National Academy of Sciences AgingGeneticsNeurochemical BiomarkersAlzheimer's DiseaseDegenerative Pathology	2008	253
Mutation Analysis of Patients with Hermansky-Pudlak Syndrome: A Frameshift Hot Spot in the HPS Gene and Apparent Locus Heterogeneity Jangsuk Oh, Lingling Ho, Sirpa Ala‐Mello, The American Journal of Human Genetics	1998	161
Complementation of Hypopigmentation in p-Mutant (Pink-Eyed Dilution) Mouse Melanocytes by Normal Human P cDNA, and Defective Complementation by OCA2 Mutant Sequences Elena V. Sviderskaya, Dorothy C. Bennett, Lingling Ho, Journal of Investigative Dermatology Knockout MouseDevelopmental BiologySignal TransductionCell SignalingPink-eyed Dilution	1997	124
Mutational Analysis of Copper Binding by Human Tyrosinase Richard A. Spritz, Lingling Ho, Minao Furumura, Journal of Investigative Dermatology Bioactive MetalCopper BindingMetalloproteinBiochemistry	1997	85
Novel mutations of the tyrosinase (TYR) gene in type I oculocutaneous albinism (OCA1) Richard A. Spritz, Jangsuk Oh, Kazuyoshi Fukai, Human Mutation Oculocutaneous AlbinismGenetic DisorderGeneticsNovel MutationsMolecular Biology	1997	71
Inhibition of Proliferation of Human Melanocytes by a KIT Antisense Oligodeoxynucleotide: Implications for Human Piebaldism and Mouse Dominant White Spotting (W) Richard A. Spritz, Lingling Ho, Kathleen M. Strunk Journal of Investigative Dermatology Signal TransductionMelanomaPathologyHuman PiebaldismKit Antisense Oligodeoxynucleotide	1994	23
Novel mutations of the tyrosinase (TYR) gene in type I oculocutaneous albinism (OCA1) Richard A. Spritz, Jangsuk Oh, Kazuyoshi Fukai, Human Mutation Oculocutaneous AlbinismGenetic DisorderGeneticsNovel MutationsMolecular Biology	1997	23
A <i>Drosophila</i> behavioral mutant, <i>down and out</i> ( <i>dao</i> ), is defective in an essential regulator of Erg potassium channels Tim Fergestad, Harinath Sale, Bret L. Bostwick, Proceedings of the National Academy of Sciences Molecular RegulationGeneticsNeurotransmitterMolecular GeneticsNeurotransmission	2010	12

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