WilliamCNicholsMD

PubMed

• 90 citations
  Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis
  Christopher J. Rhodes, Ken Batai, Marta Bleda, Matthias Haimel, Laura Southgate, Marine Germain, Michael W. Pauciulo, Charaka Hadinnapola, Jurjan Aman, Barbara Girerd,...> ;The Lancet. Respiratory Medicine. 2019 Mar 1
• Genetics and genomics of pulmonary arterial hypertension.
  Morrell, N. W.,Aldred, M. A.,Chung, W. K.,Elliott, C. G.,Nichols, W. C.,Soubrier, F.,Trembath, R. C.,Loyd, J. E.> ;Eur. Respir. J.. 2018 Dec 14
• Hypoxia-Induced Pulmonary Hypertension in Different Mouse Strains - Relation to Transcriptome.
  Ikeda, K. T.,Hale, P. T.,Pauciulo, M. W.,Dasgupta, N.,Pastura, P. A.,Le Cras, T. D.,Pandey, M. K.,Nichols, W. C.> ;Am. J. Respir. Cell Mol. Biol.. 2018 Aug 23
• 89 citations
  Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease
  Na Zhu, Carrie L. Welch, Jiayao Wang, Philip M. Allen, Claudia Gonzaga-Jauregui, Lijiang Ma, Alejandra King, Usha Krishnan, Erika B. Rosenzweig, D. Dunbar Ivy, Eric D....> ;Genome Medicine. 2018 Jul 20
• Alpha galactosidase A activity in Parkinson's disease.
  Alcalay, R. N.,Wolf, P.,Levy, O. A.,Kang, U. J.,Waters, C.,Fahn, S.,Ford, B.,Kuo, S. H.,Vanegas, N.,Shah, H.,Liong, C.,Narayan, S.,Pauciulo, M. W.,Nichols, W. C.,Gan-O...> ;Neurobiol. Dis.. 2018 Jan 26
• Neuropsychiatric characteristics of GBA-associated Parkinson disease.
  Swan M, Doan N, Ortega RA, Barrett M, Nichols W, Ozelius L, Soto-Valencia J, Boschung S, Deik A, Sarva H, Cabassa J, Johannes B, Raymond D, Marder K, Giladi N, Miravit...> ;J. Neurol. Sci.. 2016-11-15
• Glucocerebrosidase enzyme activity in GBA mutation Parkinson's disease.
  Ortega, R. A.,Torres, P. A.,Swan, M.,Nichols, W.,Boschung, S.,Raymond, D.,Barrett, M. J.,Johannes, B. A.,Severt, L.,Shanker, V.,Hunt, A. L.,Bressman, S.,Pastores, G. M...> ;J Clin Neurosci. 2016 Feb 10
• Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations.
  Alcalay RN, Levy OA, Waters CC, Fahn S, Ford B, Kuo S, Mazzoni P, Pauciulo MW, Nichols WC, Gan-Or Z, Rouleau GA, Chung WK, Wolf P, Oliva P, Keutzer J, Marder K, Zhang X> ;Brain. 2015-09-01
• The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.
  Sharp, M. E.,Caccappolo, E.,Mejia-Santana, H.,Tang, M. X.,Rosado, L.,Orbe Reilly, M.,Ruiz, D.,Louis, E. D.,Comella, C.,Nance, M.,Bressman, S.,Scott, W. K.,Tanner, C.,W...> ;Mov. Disord.. 2014 Nov 14
• Comparison of Parkinson risk in Ashkenazi Jewish patients with Gaucher disease and GBA heterozygotes.
  Alcalay RN, Dinur T, Quinn T, Sakanaka K, Levy O, Waters C, Fahn S, Dorovski T, Chung WK, Pauciulo M, Nichols W, Rana HQ, Balwani M, Bier L, Elstein D, Zimran A> ;JAMA Neurol. 2014-06-01
• Parkinson's disease with Lewy bodies associated with a heterozygous PARKIN dosage mutation.
  Sharp, M. E.,Marder, K. S.,Côté, L.,Clark, L. N.,Nichols, W. C.,Vonsattel, J. P.,Alcalay, R. N.> ;Mov. Disord.. 2014 Jan 01
• Cognitive and Motor Function in Long-Duration PARKIN-Associated Parkinson Disease
  Susan B Bressman, Steven J Frucht, Blair Ford, Lucien J Cote, Ronald F Pfeiffer, Karen S Marder, Susan F Mickel, Eric Molho, Roy N Alcalay, Michael Rezak, William C Ni...> ;JAMA. 2013 Nov 06
• Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations.
  Alcalay, R. N.,Mirelman, A.,Saunders-Pullman, R.,Tang, M. X.,Mejia Santana, H.,Raymond, D.,Roos, E.,Orbe-Reilly, M.,Gurevich, T.,Bar Shira, A.,Gana Weisz, M.,Yasinovsk...> ;Mov. Disord.. 2013 Nov 19
• A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies.
  Nalls MA, Duran R, Lopez G, Kurzawa-Akanbi M, McKeith IG, Chinnery PF, Morris CM, Theuns J, Crosiers D, Cras P, Engelborghs S, De Deyn PP, Van Broeckhoven C, Mann DMA,...> ;JAMA Neurol. 2013-06-01
• 24 citations
  Chronic Allergic Inflammation Causes Vascular Remodeling and Pulmonary Hypertension in Bmpr2 Hypomorph and Wild-Type Mice
  Elizabeth M. Mushaben, Gurjit K. Khurana Hershey, Michael W. Pauciulo, William C. Nichols, Timothy D. Le Cras> ;Plos One. 2012 Mar 9
• Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease.
  Chartier-Harlin, M. C., Dachsel, J. C., Vilariño-Güell, C., Lincoln, S. J., Leprêtre, F., Hulihan, M. M., Kachergus, J., Milnerwood, A. J., Tapia, L., Song, M. S., Le ...> ;Am J Hum Genet. 2011 Sep 9
• 58 citations
  Copy number variation in familial Parkinson disease.
  Nathan Pankratz, Alexandra Dumitriu, Kurt N. Hetrick, Mei Sun, Jeanne C. Latourelle, Jemma B. Wilk, Cheryl Halter, Kimberly F. Doheny, James F. Gusella, William C. Nic...> ;Plos One. 2011 Aug 2
• 64 citations
  High levels of placenta growth factor in sickle cell disease promote pulmonary hypertension.
  Nambirajan Sundaram, Anitaben Tailor, Laurel Mendelsohn, Janaka Wansapura, Xunde Wang, Tomoyasu Higashimoto, Michael W. Pauciulo, William M. Gottliebson, Vijay K. Kalr...> ;Blood. 2010 Jul 8
• The doctoral education of professional marriage and family therapists.
  Lee, R.E., Nichols, W.C.> ;J Marital Fam Ther. 2010 Jul 1
• 25 citations
  Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease
  David Simon, Nathan Pankratz, Diane Kissell, Michael W. Pauciulo, Cheryl Halter, Alice Rudolph, Ronald F. Pfeiffer, William C. Nichols, Tatiana Foroud> ;BMC Medical Genetics. 2010 Apr 1
• 89 citations
  Genomewide association study for onset age in Parkinson disease
  Jeanne C. Latourelle, Nathan Pankratz, Alexandra Dumitriu, Jemma B. Wilk, Stefano Goldwurm, Gianni Pezzoli, Claudio Mariani, Anita L. DeStefano, Cheryl Halter, James F...> ;BMC Medical Genetics. 2009 Sep 22
• 63 citations
  Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations
  Nathan Pankratz, Diane Kissell, Michael W. Pauciulo, Cheryl Halter, Alice Rudolph, Ronald F. Pfeiffer, Karen Marder, Tatiana Foroud, William C. Nichols> ;Neurology. 2009 Jul 28
• 32 citations
  Alpha-synuclein and familial Parkinson's disease.
  Nathan Pankratz, William C. Nichols, V. E. Elsaesser, Michael W. Pauciulo, Diane K. Marek, Cheryl Halter, Joanne Wojcieszek, Alice Rudolph, Ronald F. Pfeiffer, Tatiana...> ;Movement Disorders. 2009 Jun 15
• 34 citations
  Variation in GIGYF2 is not associated with Parkinson disease
  William C. Nichols, Diane Kissell, Nathan Pankratz, Michael W. Pauciulo, V. E. Elsaesser, Kristi A. Clark, Cheryl Halter, Alice Rudolph, Joanne Wojcieszek, Ronald F. P...> ;Neurology. 2009 Jun 2
• 344 citations
  Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
  Nathan Pankratz, Jemma B. Wilk, Jeanne C. Latourelle, Anita L. DeStefano, Cheryl Halter, Elizabeth W. Pugh, Kimberly F. Doheny, James F. Gusella, William C. Nichols, T...> ;Human Genetics. 2009 Jan 1
• Join now to see all