JonathanAGreenbergMD

PubMed

• 2 citations
  Quantifying Environmental Limiting Factors on Tree Cover Using Geospatial Data
  Jonathan A. Greenberg, Maria José Santos, Solomon Z. Dobrowski, Vern C. Vanderbilt, Susan L. Ustin> ;Plos One. 2015 Feb 18
• Correlations of salivary biomarkers with clinical assessments in patients with cystic fibrosis.
  Nie S, Zhang H, Mayer KM, Oppenheim FG, Little FF, Greenberg J, Uluer AZ, Walt DR> ;PLoS ONE. 2015-01-01
• 79 citations
  The climate velocity of the contiguous United States during the 20th century.
  Solomon Z. Dobrowski, John T. Abatzoglou, Alan Swanson, Jonathan A. Greenberg, Alison R. Mynsberge, Zachary A. Holden, Michael K. Schwartz> ;Global Change Biology. 2013 Jan 1
• "Mind the trap": mindfulness practice reduces cognitive rigidity.
  Greenberg J, Reiner K, Meiran N> ;PLoS ONE. 2012-01-01
• 198 citations
  Changes in Climatic Water Balance Drive Downhill Shifts in Plant Species’ Optimum Elevations
  Shawn M. Crimmins, Solomon Z. Dobrowski, Jonathan A. Greenberg, John T. Abatzoglou, Alison R. Mynsberge> ;Science. 2011 Jan 21
• 30 citations
  Distribution of Y chromosomes among native North Americans: A study of Athapaskan population history
  Ripan S. Malhi, Angélica González-Oliver, Kari Britt Schroeder, Brian M. Kemp, Jonathan A. Greenberg, Solomon Z. Dobrowski, David Glenn Smith, Andrés Reséndez, Tatiana...> ;American Journal of Physical Anthropology. 2008 Dec 1
• Retinal degenerative disorders in Southern Africa: a molecular genetic approach.
  Ramesar RS, Roberts L, Rebello G, Goliath R, Vorster A, September A, Ehrenreich L, Gama D, Greenberg J> ;Adv. Exp. Med. Biol.. 2003-01-01
• CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.
  Astuto LM, Bork JM, Weston MD, Askew JW, Fields RR, Orten DJ, Ohliger SJ, Riazuddin S, Morell RJ, Khan S, Riazuddin S, Kremer H, van Hauwe P, Moller CG, Cremers CWRJ, ...> ;Am. J. Hum. Genet.. 2002-08-01
• 59 citations
  The Structure of Diversity within New World Mitochondrial DNA Haplogroups: Implications for the Prehistory of North America
  Ripan S. Malhi, Jason Eshleman, Jonathan A. Greenberg, Deborah A. Weiss, Beth A. Schultz Shook, Frederika A. Kaestle, Joseph G. Lorenz, Brian M. Kemp, John R. Johnson,...> ;American Journal of Human Genetics. 2002 Apr 1
• Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).
  McKie AB, McHale JC, Keen TJ, Tarttelin EE, Goliath R, van Lith-Verhoeven JJ, Greenberg J, Ramesar RS, Hoyng CB, Cremers FP, Mackey DA, Bhattacharya SS, Bird AC, Markh...> ;Hum. Mol. Genet.. 2001-07-15
• Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.
  Astuto LM, Weston MD, Carney CA, Hoover DM, Cremers CW, Wagenaar M, Moller C, Smith RJ, Pieke-Dahl S, Greenberg J, Ramesar R, Jacobson SG, Ayuso C, Heckenlively JR, Ta...> ;Am. J. Hum. Genet.. 2000-12-01
• Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa.
  Weston MD, Eudy JD, Fujita S, Yao S, Usami S, Cremers C, Greenberg J, Ramesar R, Martini A, Moller C, Smith RJ, Sumegi J, Kimberling WJ, Greenburg J> ;Am. J. Hum. Genet.. 2000-04-01
• A photoreceptor gene mutation in an indigenous black African family with retinitis pigmentosa identified using a rapid screening approach for common rhodopsin mutations.
  Greenberg J, Franz T, Goliath R, Ramesar R> ;S. Afr. Med. J.. 1999-08-01
• Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations.
  DeStefano AL, Cupples LA, Arnos KS, Asher JH, Baldwin CT, Blanton S, Carey ML, da Silva EO, Friedman TB, Greenberg J, Lalwani AK, Milunsky A, Nance WE, Pandya A, Rames...> ;Hum. Genet.. 1998-05-01
• Rhodopsin mutation G109R in a family with autosomal dominant retinitis pigmentosa.
  Goliath R, Bardien S, September A, Martin R, Ramesar R, Greenberg J> ;Hum. Mutat.. 1998-01-01
• Familial streptomycin ototoxicity in a South African family: a mitochondrial disorder.
  Gardner JC, Goliath R, Viljoen D, Sellars S, Cortopassi G, Hutchin T, Greenberg J, Beighton P> ;J. Med. Genet.. 1997-11-01
• The gene for PEDF, a retinal growth factor is a prime candidate for retinitis pigmentosa and is tightly linked to the RP13 locus on chromosome 17p13.3.
  Goliath R, Tombran-Tink J, Rodriquez IR, Chader G, Ramesar R, Greenberg J> ;Mol. Vis.. 1996-06-19
• Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity.
  Ramesar RS, Greenberg J, Martin R, Goliath R, Bardien S, Mundlos S, Beighton P> ;J. Med. Genet.. 1996-06-01
• Fine localization of the locus for autosomal dominant retinitis pigmentosa on chromosome 17p.
  Goliath R, Shugart Y, Janssens P, Weissenbach J, Beighton P, Ramasar R, Greenberg J> ;Am. J. Hum. Genet.. 1995-10-01
• An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q.
  Bardien S, Ebenezer N, Greenberg J, Inglehearn CF, Bartmann L, Goliath R, Beighton P, Ramesar R, Bhattacharya SS> ;Hum. Mol. Genet.. 1995-08-01
• Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.
  Farrer LA, Arnos KS, Asher JH, Baldwin CT, Diehl SR, Friedman TB, Greenberg J, Grundfast KM, Hoth C, Lalwani AK> ;Am. J. Hum. Genet.. 1994-10-01
• A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17.
  Greenberg J, Goliath R, Beighton P, Ramesar R> ;Hum. Mol. Genet.. 1994-06-01
• Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11.
  Kimberling WJ, Möller CG, Davenport S, Priluck IA, Beighton PH, Greenberg J, Reardon W, Weston MD, Kenyon JB, Grunkemeyer JA> ;Genomics. 1992-12-01
• Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism.
  Spritz RA, Holmes SA, Ramesar R, Greenberg J, Curtis D, Beighton P> ;Am. J. Hum. Genet.. 1992-11-01
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