Harvard Catalyst Profiles

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Patricia E. Greenstein, M.D.


Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
  1. Ahtam B, Waisbren SE, Anastasoaie V, Berry GT, Brown M, Petrides S, Afacan O, Prabhu SP, Schomer D, Grant PE, Greenstein PE. Identification of neuronal structures and pathways corresponding to clinical functioning in galactosemia. J Inherit Metab Dis. 2020 11; 43(6):1205-1218. PMID: 32592186.
    Citations:    Fields:    
  2. Greenstein PE. Commentary on An Elderly Man with Dementia. Clin Chem. 2020 03 01; 66(3):415-420. PMID: 32109301.
    Citations:    Fields:    Translation:Humans
  3. Martucci MG, McIlduff CE, Shin C, Gutierrez HV, Nam JY, Greenstein P, Phillips K, Uhlmann EJ, Wong ET, Rutkove SB. Quantitative ultrasound of muscle can detect corticosteroid effects. Clin Neurophysiol. 2019 08; 130(8):1460-1464. PMID: 31122815.
    Citations: 1     Fields:    Translation:Humans
  4. Maragkos GA, Alturki AY, Greenstein PE, Enriquez-Marulanda A, Kicielinski KJ, Moore JM, Ogilvy CS, Thomas AJ. Percutaneous Transverse Sinus Cannulation for Dural Arteriovenous Fistula Coiling: Operative Video. World Neurosurg. 2019 Jul; 127:335. PMID: 30995549.
    Citations:    Fields:    Translation:Humans
  5. Manor B, Greenstein PE, Davila-Perez P, Wakefield S, Zhou J, Pascual-Leone A. Repetitive Transcranial Magnetic Stimulation in Spinocerebellar Ataxia: A Pilot Randomized Controlled Trial. Front Neurol. 2019; 10:73. PMID: 30809184.
    Citations: 7     
  6. Zesiewicz TA, Wilmot G, Kuo SH, Perlman S, Greenstein PE, Ying SH, Ashizawa T, Subramony SH, Schmahmann JD, Figueroa KP, Mizusawa H, Schöls L, Shaw JD, Dubinsky RM, Armstrong MJ, Gronseth GS, Sullivan KL. Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology. Neurology. 2018 03 06; 90(10):464-471. PMID: 29440566.
    Citations: 20     Fields:    Translation:Humans
  7. Waisbren SE, Prabhu SP, Greenstein P, Petty C, Schomer D, Anastasoaie V, Charette K, Rodriguez D, Merugumala S, Lin AP. Improved Measurement of Brain Phenylalanine and Tyrosine Related to Neuropsychological Functioning in Phenylketonuria. JIMD Rep. 2017; 34:77-86. PMID: 27677920.
    Citations: 2     
  8. Farzan F, Wu Y, Manor B, Anastasio EM, Lough M, Novak V, Greenstein PE, Pascual-Leone A. Cerebellar TMS in treatment of a patient with cerebellar ataxia: evidence from clinical, biomechanics and neurophysiological assessments. Cerebellum. 2013 Oct; 12(5):707-12. PMID: 23625327.
    Citations: 13     Fields:    Translation:Humans
  9. Zesiewicz TA, Greenstein PE, Sullivan KL, Wecker L, Miller A, Jahan I, Chen R, Perlman SL. A randomized trial of varenicline (Chantix) for the treatment of spinocerebellar ataxia type 3. Neurology. 2012 Feb 21; 78(8):545-50. PMID: 22323747.
    Citations: 33     Fields:    Translation:Humans
  10. Waisbren SE, Potter NL, Gordon CM, Green RC, Greenstein P, Gubbels CS, Rubio-Gozalbo E, Schomer D, Welt C, Anastasoaie V, D'Anna K, Gentile J, Guo CY, Hecht L, Jackson R, Jansma BM, Li Y, Lip V, Miller DT, Murray M, Power L, Quinn N, Rohr F, Shen Y, Skinder-Meredith A, Timmers I, Tunick R, Wessel A, Wu BL, Levy H, Elsas L, Berry GT. The adult galactosemic phenotype. J Inherit Metab Dis. 2012 Mar; 35(2):279-86. PMID: 21779791.
    Citations: 53     Fields:    Translation:HumansPHPublic Health
  11. Sengupta S, Pedersen NP, Davis JE, Rojas R, Reddy H, Kasper E, Greenstein P, Wong ET. Illusion of stroke: intravascular lymphomatosis. Rev Neurol Dis. 2011; 8(3-4):e107-13. PMID: 22249564.
    Citations: 1     Fields:    Translation:Humans
  12. Greenstein PE, Vonsattel JP, Margolis RL, Joseph JJ . HDL2 Neuropathology. Movement Disorders, In. 2007; In press.
  13. Greenstein PE. Neurogenetics. Neurology Review for Psychiatrists. Editors: Ronthal MR and Savitz SL. 2007; In press.
  14. Byrnes V, Afdhal N, Challies T, Greenstein PE. Drug induced liver injury secondary to interferon-beta (IFN-beta) in multiple sclerosis. Ann Hepatol. 2006 Jan-Mar; 5(1):56-9. PMID: 16531969.
    Citations: 5     Fields:    Translation:Humans
  15. Margolis RL, Holmes SE, Rosenblatt A, Gourley L, O'Hearn E, Ross CA, Seltzer WK, Walker RH, Ashizawa T, Rasmussen A, Hayden M, Almqvist EW, Harris J, Fahn S, MacDonald ME, Mysore J, Shimohata T, Tsuji S, Potter N, Nakaso K, Adachi Y, Nakashima K, Bird T, Krause A, Greenstein P. Huntington's Disease-like 2 (HDL2) in North America and Japan. Ann Neurol. 2004 Nov; 56(5):670-4. PMID: 15468075.
    Citations: 22     Fields:    Translation:HumansCells
  16. Greenstein P. The Development of a Neurogenetics Curriculum using MyCourses for HMS students. Academy Day Plenary Session. Harvard Medical School, Boston MA. 2003.
  17. Greenstein PE, Joseph JT and Margolis RL. Genotype-Phenotype Correlations in HDL2. American Academy of Neurology Meetings. San Francisco, CA. 2003.
  18. Greenstein P. Tick paralysis. Med Clin North Am. 2002 Mar; 86(2):441-6. PMID: 11982312.
    Citations: 1     Fields:    Translation:HumansAnimals
  19. Greenstein P. Tick Paralysis. The Medical Clinics of North America: Tick Borne Diseases. Editor: Edlow JA. 2002; 441-447.
  20. Karadimas CL, Greenstein P, Sue CM, Joseph JT, Tanji K, Haller RG, Taivassalo T, Davidson MM, Shanske S, Bonilla E, DiMauro S. Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA. Neurology. 2000 Sep 12; 55(5):644-9. PMID: 10980727.
    Citations: 17     Fields:    Translation:Humans
  21. Karadimas CL, Greenstein P, Joseph JT, Bonilla E, Tanji K, Shanske S, Sue SM and Dimauro S. A novel missense mutation in the mtDNA COX1 gene: Another cause of myopathy with myoglobinuria. American Society of Human Genetics Meetings. San Francisco, CA. 1999.
  22. Ronthal M and Greenstein P. Myoclonus and Asterixis. Movement Disorders in Neurology and Psychiatry Editors: Joseph AB, Young RR. 1998; 449-456.
  23. Joseph JT, Richards CS, Anthony DC, Upton M, Perez-Atayde AR, Greenstein P. Congenital myotonic dystrophy pathology and somatic mosaicism. Neurology. 1997 Nov; 49(5):1457-60. PMID: 9371942.
    Citations: 4     Fields:    Translation:HumansCells
  24. Greenstein PE, Moore D, Levy-Lohad E, Stephens K, Bird TD. Nine families with the SCA3/Machado-Joseph disease type of inherited ataxia. Neurology. 1996 Oct; 47(4):1106-7. PMID: 8857759.
    Citations:    Fields:    Translation:Humans
  25. Ekker SC, Ungar AR, Greenstein P, von Kessler DP, Porter JA, Moon RT, Beachy PA. Patterning activities of vertebrate hedgehog proteins in the developing eye and brain. Curr Biol. 1995 Aug 01; 5(8):944-55. PMID: 7583153.
    Citations: 125     Fields:    Translation:AnimalsCells
  26. Kelly GM, Greenstein P, Erezyilmaz DF, Moon RT. Zebrafish wnt8 and wnt8b share a common activity but are involved in distinct developmental pathways. Development. 1995 Jun; 121(6):1787-99. PMID: 7600994.
    Citations: 58     Fields:    Translation:AnimalsCells
  27. Greenstein P and Bird TD. The New Molecular Biology of Neurological Disease. Focus and Opinion: Internal Medicine. 1995; 3:178-186.
  28. Greenstein P and Bird TD. Neurogenetics: triumphs and Challenges. Western Journal of Medicine. 1995; 161(3):242-246.
  29. Greenstein P, Levy-Lahad E, Ranum, L and Bird, TD. Remarkable phenotypic heterogeneity in two families with non-Portuguese Machado Joseph Disease. World Federation Meetings of Neurogenetics. Seattle, WA. 1995.
  30. Kelly GM, Greenstein P, Erezylimas DF and Moon RT. Expression of wnt8 and wnt8b during zebrafish embryogenesis. Zebrafish Development and Genetics Meetings, Cold Spring Harbor Labs, Long Island, NY. 1994.
  31. Saver JL, Greenstein P, Ronthal M, Mesulam MM. Asymmetric catalepsy after right hemisphere stroke. Mov Disord. 1993; 8(1):69-73. PMID: 8419810.
    Citations: 4     Fields:    Translation:Humans
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.