Joe J. Hoo - Concepedia

Author

Joe J. Hoo

SUNY Upstate Medical University

Also Known As

J J Hoo, J. Hoo, J. J. HOO, J. J. Hoo, J.C.B. Hoo, J.J. Hoo, Joe Hoo, Joe J Hoo, Joe J. Hoo, Joe Jie Hoo

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

SUNY Upstate Medical University University of Calgary Rush University Medical Center University of Illinois Chicago Syracuse University

About

Joe J. Hoo is an author at SUNY Upstate Medical University specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	18	1.4K
2	Social Sciences	2	2	698
3	Natural Sciences	1	1	23
4	Public Health	1	1	15
5	Biochemistry	1	1	27

Joe J. Hoo

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay Santhosh Girirajan, Jill A. Rosenfeld, Gregory M. Cooper, Nature Genetics Developmental BiologyTwo-hit ModelGeneticsDevelopmental ScienceGlobal Developmental Delay	2010	669
Tiny interstitial duplication of proximal 7q in association with a maternal paracentric inversion Joe J. Hoo, R. Lorenz, Angelika Fischer, Human Genetics InfertilityMaternal Paracentric InversionGenetic DisorderGeneticsGynecology	1982	137
Twin brothers with MIDAS syndrome and XX karyotype Arturo Anguiano, Xiaojing Yang, J.K. Felix, American Journal of Medical Genetics Part A	2002	100
Recurrent de novo interstitial deletion of 16q in two mentally retarded sisters Joe J. Hoo, R. Brian Lowry, Ching‐Shwun Lin, Clinical Genetics Developmental AnomalyDevelopmental BiologyRetarded SistersPsychiatrySimilar Clinical Features	1985	91
KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation Mustapha Amyere, Thomas Vogt, Joe J. Hoo, Journal of Investigative Dermatology Mendelian DisorderGenetic DisorderGeneticsMolecular GeneticsMedicine	2011	85
Tentative assignment of piebald trait gene to chromosome band 4q12 Joe J. Hoo, Robert H. A. Haslam, C. van Orman Human Genetics CytogeneticsGenetic DisorderGeneticsEvolutionary BiologyLinkage Analysis	1986	54
Four new cases of inverted terminal duplication: A modified hypothesis of mechanism of origin Joe J. Hoo, Margaret Chao, Katarina Szego, American Journal of Medical Genetics	1995	46
A gene for FG syndrome maps in the Xq12-q21.31 region Sylvain Briault, Ruth F. Hill, Antony E. Shrimpton, American Journal of Medical Genetics GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification	1997	45
FG syndrome, an X-linked multiple congenital anomaly syndrome: The clinical phenotype and an algorithm for diagnostic testing Robin D. Clark, John M. Graham, Michael J. Friez, Genetics in Medicine Down SyndromeDevelopmental AnomalyMendelian DisorderGenetic DisorderFg Syndrome	2009	41
Determining the origins and the structural aberrations of small marker chromosomes in two cases of 45,X/46,X, +mar by use of chromosome‐specific DNA probes Cheng‐Chieh Lin, Juliane Meyne, Ramakrishnan Sasi, American Journal of Medical Genetics	1990	38

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