Tim Donlon - Concepedia

Author

Tim Donlon

Also Known As

Donlon T, Farrell, Joseph, T A Donlon, T Donlon, T. A. Donlon, T. DONLON, T. Donlon, T.A. Donlon, Tim A. Donlon, Tim Donlon

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Stanford University Boston Children's Hospital Harvard University University of Hawaiʻi at Mānoa Howard Hughes Medical Institute

About

Tim Donlon is an author at Stanford University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	912
2	Natural Sciences	4	4	424
3	Cell Biology	3	3	119
4	Biochemistry	1	1	25
5	Biology	1	1	36

Tim Donlon

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region Tayfun Özçelık, Stuart E. Leff, Wendy P. Robinson, Nature Genetics Small Nuclear RibonucleoproteinTranscriptional RegulationGenetic DisorderNatural SciencesGenetics	1992	295
Maintenance treatment of patients with myelodysplastic syndromes using recombinant human granulocyte colony-stimulating factor RS Negrin, DH Haeuber, Arnon Nagler, Blood	1990	233
Performance‐Based Measures of Physical Function for High‐Function Populations J. David Curb, Clementina D. Ceria‐Ulep, Beatriz L. Rodríguez, Journal of the American Geriatrics Society	2006	215
Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome. Tim Donlon, M. Lalande, Arlene R. Wyman, Proceedings of the National Academy of Sciences CytogeneticsGeneticsPathologyMolecular GeneticsDisease Gene Identification	1986	159
Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes Tim Donlon Human Genetics Chromosome 15Q11.2Similar Molecular DeletionsGenetic DisorderGeneticsPathology	1988	97
Differential amplification, assembly, and relocation of multiple DNA sequences in human neuroblastomas and neuroblastoma cell lines. Yosef Shiloh, Janet Shipley, Garrett M. Brodeur, Proceedings of the National Academy of Sciences CytogeneticsComplex Amplification MechanismMolecular BiologyPathologyGlioma	1985	82
Localization of the Gene Encoding the Human Interleukin-2 Receptor on Chromosome 10 Warren J. Leonard, Tim Donlon, Roger V. Lebo, Science	1985	77
Prader-Willi Syndrome Is Caused by Disruption of the SNRPN Gene C.D. Kuslich, J. Kobori, Gayatry Mohapatra, The American Journal of Human Genetics Transcriptional RegulationRare DiseasesMendelian DisorderDisease MechanismGenetic Disorder	1999	75
Moderately repeated DNA sequences specific for the short arm of the human Y chromosome are present in XX males and reduced in copy number in an XY female Ulrich Müller, Marc Lalande, Tim Donlon, Nucleic Acids Research	1986	71
Assignment of the human ?-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33?36 Yosef Shiloh, Tim Donlon, G Bruns, Human Genetics ChromatinGenetic DisorderGeneticsRegion Q33Genome Structure	1986	66

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