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Paul S. Ing

Observed names: P S Ing, P. S. Ing, P.S. Ing, PAUL S. ING, Paul Ing
OpenAlex ID: A5080926571
Familial Dyslexia: Use of Genetic Linkage Data to Define Subtypes
1990 · SHELLEY D. SMITH, BRUCE F. PENNINGTON, et al. · Journal of the American Academy of Child & Adolescent Psychiatry · 104
Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41.
1995 · W J Kimberling, M D Weston, et al. · PubMed Central · 64
The Genomic Structure of the Gene Defective in Usher Syndrome Type Ib (MYO7A)
1997 · Philip M. Kelley, Mike D. Weston, et al. · Genomics · 44
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Narrowing the Genetic Interval and Yeast Artificial Chromosome Map in the Branchio–Oto–Renal Region on Chromosome 8q
1996 · Shrawan Kumar, William J. Kimberling, et al. · Genomics · 21
Cat‐eye syndrome with different marker chromosomes in a mother and daughter
1987 · Paul S. Ing, Mark S. Lubinsky, et al. · American Journal of Medical Genetics · 20
Human chromosome classification using discriminant analysis and Bayesian probability
1980 · Robert S. Ledley, Paul S. Ing, et al. · Computers in Biology and Medicine · 19
Statement of the American College of Medical Genetics on Universal Newborn Hearing Screening
2000 · Walter E. Nance, George C. Cunningham, et al. · Genetics in Medicine · 18
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Cytogentic studies of a patient with mosaicism of isochromosome 13q and a dicentric (Y; 13) translocation showing differential centromeric activity
1983 · Paul S. Ing, Shelley D. Smith · Clinical Genetics · 18
Detection of Mosaicism in amniotic fluid cultures: A CYT02000 collaborative study
1999 · Paul S. Ing, Daniel L. Van Dyke, et al. · Genetics in Medicine · 11
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A comment on the analysis of families with prelinqual deafness.
1989 · S Kimberling, S D Smith, et al. · Europe PMC (PubMed Central) · 5
The ACMG CYTO2000 subcommittee?
1998 · Andrew T.L. Chen, Paul S. Ing, et al. · Genetics in Medicine · 3
Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practices
2005 · Samuel P. Caudill, Daniel L. Van Dyke, et al. · Statistics in Medicine · 1
Hereditary Hearing Impairment
1995 · P. S. Ing · Archives of Otolaryngology - Head and Neck Surgery · 1
Data collection in the Great Plains Genetics Service Network: using limited funds to collect data from centers with varying resources.
1991 · P S Ing, J M Smith · PubMed Central · 1
Availability of genetic services to the deaf
1989 · Paul S. Ing, Melanie L. Lempke, et al. · American Journal of Medical Genetics · 1
Cyto 2000 – A Collaborative study for the evaluation of blood chromosome mosaicism
2000 · S. Schwartz, P.S. Ing, et al. · Genetics in Medicine
Physical mapping and isolation of candidate genes surrounding the BOR locus on human chromosome 8q13
1996 · Sushil Kumar, W. J. Kimberling, et al.
National Deaf Register as a Resource for Hereditary Deafness Research
1991 · PAUL S. ING, BRENDA M. WERNIMONT, et al. · Annals of the New York Academy of Sciences
Works count: 18
Citation count: 331
H-index: 9
I10-index: 9
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