Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry
Lee, Annie J., Wang, Yuanjia, Alcalay, Roy N., Mejia‐Santana, Helen, Saunders‐Pullman, Rachel, Bressman, Susan, Corvol, Jean‐Christophe, Brice, Alexis, Lesage, Suzanne, Mangone, Graziella, Tolosa, Eduardo, Pont‐Sunyer, Claustre, Vilas, Dolores, Schüle, Birgitt, Kausar, Farah, Foroud, Tatiana, Berg, Daniela, Brockmann, Kathrin, Goldwurm, Stefano, Siri, Chiara, Asselta, Rosanna, Ruiz‐Martinez, Javier, Mondragón, Elisabet, Marras, Connie, Ghate, Taneera, Giladi, Nir, Mirelman, Anat, Marder, Karen
Published in Movement disorders (01.10.2017)
Published in Movement disorders (01.10.2017)
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The association between Mediterranean diet adherence and Parkinson's disease
Alcalay, Roy N., Gu, Yian, Mejia-Santana, Helen, Cote, Lucien, Marder, Karen S., Scarmeas, Nikolaos
Published in Movement disorders (01.05.2012)
Published in Movement disorders (01.05.2012)
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Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controls
Agalliu, Ilir, Ortega, Roberto A., Luciano, Marta San, Mirelman, Anat, Pont‐Sunyer, Claustre, Brockmann, Kathrin, Vilas, Dolores, Tolosa, Eduardo, Berg, Daniela, Warø, Bjørg, Glickman, Amanda, Raymond, Deborah, Inzelberg, Rivka, Ruiz‐Martinez, Javier, Mondragon, Elisabet, Friedman, Eitan, Hassin‐Baer, Sharon, Alcalay, Roy N., Mejia‐Santana, Helen, Aasly, Jan, Foroud, Tatiana, Marder, Karen, Giladi, Nir, Bressman, Susan, Saunders‐Pullman, Rachel
Published in Movement disorders (01.09.2019)
Published in Movement disorders (01.09.2019)
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The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study
Sharp, Madeleine E., Caccappolo, Elise, Mejia-Santana, Helen, Tang, Ming-X., Rosado, Llency, Orbe Reilly, Martha, Ruiz, Diana, Louis, Elan D., Comella, Cynthia, Nance, Martha, Bressman, Susan, Scott, William K., Tanner, Caroline, Waters, Cheryl, Fahn, Stanley, Cote, Lucien, Ford, Blair, Rezak, Michael, Novak, Kevin, Friedman, Joseph H., Pfeiffer, Ronald, Payami, Haydeh, Molho, Eric, Factor, Stuart A., Nutt, John, Serrano, Carmen, Arroyo, Maritza, Pauciulo, Michael W., Nichols, William C., Clark, Lorraine N., Alcalay, Roy N., Marder, Karen S.
Published in Movement disorders (01.02.2015)
Published in Movement disorders (01.02.2015)
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Genetic and Clinical Predictors of Deep Brain Stimulation in Young-Onset Parkinson's Disease
Pal, Gian D., Hall, Deborah, Ouyang, Bichun, Phelps, Jessica, Alcalay, Roy, Pauciulo, Michael W., Nichols, William C., Clark, Lorraine, Mejia-Santana, Helen, Blasucci, Lucia, Goetz, Christopher G., Comella, Cynthia, Colcher, Amy, Gan-Or, Ziv, Rouleau, Guy A., Marder, Karen
Published in Movement disorders clinical practice (Hoboken, N.J.) (01.09.2016)
Published in Movement disorders clinical practice (Hoboken, N.J.) (01.09.2016)
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Application of the Movement Disorder Society prodromal criteria in healthy G2019S‐LRRK2 carriers
Mirelman, Anat, Saunders‐Pullman, Rachel, Alcalay, Roy N., Shustak, Shiran, Thaler, Avner, Gurevich, Tanya, Raymond, Deborah, Mejia‐Santana, Helen, Orbe Reilly, Martha, Ozelius, Laurie, Clark, Lorraine, Gana‐Weisz, Mali, Bar‐Shira, Anat, Orr‐Utreger, Avi, Bressman, Susan B., Marder, Karen, Giladi, Nir
Published in Movement disorders (01.07.2018)
Published in Movement disorders (01.07.2018)
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Journal Article
Age-specific penetrance of LRRK2 G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium
Marder, Karen, Wang, Yuanjia, Alcalay, Roy N, Mejia-Santana, Helen, Tang, Ming-Xin, Lee, Annie, Raymond, Deborah, Mirelman, Anat, Saunders-Pullman, Rachel, Clark, Lorraine, Ozelius, Laurie, Orr-Urtreger, Avi, Giladi, Nir, Bressman, Susan
Published in Neurology (07.07.2015)
Published in Neurology (07.07.2015)
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Journal Article
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease
Lai, Dongbing, Alipanahi, Babak, Fontanillas, Pierre, Schwantes‐An, Tae‐Hwi, Aasly, Jan, Alcalay, Roy N., Beecham, Gary W., Berg, Daniela, Bressman, Susan, Brice, Alexis, Brockman, Kathrin, Clark, Lorraine, Cookson, Mark, Das, Sayantan, Van Deerlin, Vivianna, Follett, Jordan, Farrer, Matthew J., Trinh, Joanne, Gasser, Thomas, Goldwurm, Stefano, Gustavsson, Emil, Klein, Christine, Lang, Anthony E., Langston, J. William, Latourelle, Jeanne, Lynch, Timothy, Marder, Karen, Marras, Connie, Martin, Eden R., McLean, Cory Y., Mejia‐Santana, Helen, Molho, Eric, Myers, Richard H., Nuytemans, Karen, Ozelius, Laurie, Payami, Haydeh, Raymond, Deborah, Rogaeva, Ekaterina, Rogers, Michael P., Ross, Owen A., Samii, Ali, Saunders‐Pullman, Rachel, Schüle, Birgitt, Schulte, Claudia, Scott, William K., Tanner, Caroline, Tolosa, Eduardo, Tomkins, James E., Vilas, Dolores, Trojanowski, John Q., Uitti, Ryan, Vance, Jeffery M., Visanji, Naomi P., Wszolek, Zbigniew K., Zabetian, Cyrus P., Mirelman, Anat, Giladi, Nir, Orr Urtreger, Avi, Cannon, Paul, Fiske, Brian, Foroud, Tatiana
Published in Annals of neurology (01.07.2021)
Published in Annals of neurology (01.07.2021)
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Journal Article
Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations
Alcalay, Roy N., Mirelman, Anat, Saunders-Pullman, Rachel, Tang, Ming-X, Mejia Santana, Helen, Raymond, Deborah, Roos, Ernest, Orbe-Reilly, Martha, Gurevich, Tanya, Bar Shira, Anat, Gana Weisz, Mali, Yasinovsky, Kira, Zalis, Maayan, Thaler, Avner, Deik, Andres, Barrett, Matthew James, Cabassa, Jose, Groves, Mark, Hunt, Ann L., Lubarr, Naomi, San Luciano, Marta, Miravite, Joan, Palmese, Christina, Sachdev, Rivka, Sarva, Harini, Severt, Lawrence, Shanker, Vicki, Swan, Matthew Carrington, Soto-Valencia, Jeannie, Johannes, Brooke, Ortega, Robert, Fahn, Stanley, Cote, Lucien, Waters, Cheryl, Mazzoni, Pietro, Ford, Blair, Louis, Elan, Levy, Oren, Rosado, Llency, Ruiz, Diana, Dorovski, Tsvyatko, Pauciulo, Michael, Nichols, William, Orr-Urtreger, Avi, Ozelius, Laurie, Clark, Lorraine, Giladi, Nir, Bressman, Susan, Marder, Karen S.
Published in Movement disorders (01.12.2013)
Published in Movement disorders (01.12.2013)
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Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene
Mirelman, Anat, Alcalay, Roy N., Saunders-Pullman, Rachel, Yasinovsky, Kira, Thaler, Avner, Gurevich, Tanya, Mejia-Santana, Helen, Raymond, Deborah, Gana-Weisz, Mali, Bar-Shira, Anat, Ozelius, Laurie, Clark, Lorraine, Orr-Urtreger, Avi, Bressman, Susan, Marder, Karen, Giladi, Nir
Published in Movement disorders (01.06.2015)
Published in Movement disorders (01.06.2015)
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REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers
Saunders-Pullman, Rachel, Alcalay, Roy N., Mirelman, Anat, Wang, Cuiling, Luciano, Marta San, Ortega, Roberto A., Glickman, Amanda, Raymond, Deborah, Mejia-Santana, Helen, Doan, Nancy, Johannes, Brooke, Yasinovsky, Kira, Ozelius, Laurie, Clark, Lorraine, Orr-Utreger, Avi, Marder, Karen, Giladi, Nir, Bressman, Susan B.
Published in Movement disorders (01.11.2015)
Published in Movement disorders (01.11.2015)
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Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's disease
Alcalay, Roy N, Mejia-Santana, Helen, Mirelman, Anat, Saunders-Pullman, Rachel, Raymond, Deborah, Palmese, Christina, Caccappolo, Elise, Ozelius, Laurie, Orr-Urtreger, Avi, Clark, Lorraine, Giladi, Nir, Bressman, Susan, Marder, Karen
Published in Parkinsonism & related disorders (01.02.2015)
Published in Parkinsonism & related disorders (01.02.2015)
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Interest in Genetic Testing in Ashkenazi Jewish Parkinson’s Disease Patients and Their Unaffected Relatives
Gupte, Manisha, Alcalay, Roy N., Mejia-Santana, Helen, Raymond, Deborah, Saunders-Pullman, Rachel, Roos, Ernest, Orbe-Reily, Martha, Tang, Ming-X, Mirelman, Anat, Ozelius, Laurie, Orr-Urtreger, Avi, Clark, Lorraine, Giladi, Nir, Bressman, Susan, Marder, Karen
Published in Journal of genetic counseling (01.04.2015)
Published in Journal of genetic counseling (01.04.2015)
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Differences in performance on English and Hebrew versions of the MoCA in Parkinson's patients
Xu, Yaqian, Mirelman, Anat, Saunders-Pullman, Rachel, Mejia-Santana, Helen, Caccappolo, Elise, Raymond, Deborah, Giladi, Nir, Bressman, Susan, Marder, Karen, Alcalay, Roy N.
Published in Clinical parkinsonism & related disorders (01.01.2020)
Published in Clinical parkinsonism & related disorders (01.01.2020)
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Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?
Saunders‐Pullman, Rachel, Mirelman, Anat, Wang, Cuiling, Alcalay, Roy N., San Luciano, Marta, Ortega, Robert, Raymond, Deborah, Mejia‐Santana, Helen, Ozelius, Laurie, Clark, Lorraine, Orr‐Utreger, Avi, Marder, Karen, Giladi, Nir, Bressman, Susan B.
Published in Annals of clinical and translational neurology (01.09.2014)
Published in Annals of clinical and translational neurology (01.09.2014)
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Familial aggregation of early‐ and late‐onset Parkinson's disease
Marder, Karen, Levy, Gilberto, Louis, Elan D., Mejia‐Santana, Helen, Cote, Lucien, Andrews, Howard, Harris, Juliette, Waters, Cheryl, Ford, Blair, Frucht, Steven, Fahn, Stanley, Ottman, Ruth
Published in Annals of neurology (01.10.2003)
Published in Annals of neurology (01.10.2003)
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Pilot association study of the β-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity
Clark, Lorraine N., Nicolai, Angelique, Afridi, Shehla, Harris, Juliette, Mejia-Santana, Helen, Strug, Lisa, Cote, Lucien J., Louis, Elan D., Andrews, Howard, Waters, Cheryl, Ford, Blair, Frucht, Steven, Fahn, Stanley, Mayeux, Richard, Ottman, Ruth, Marder, K.
Published in Movement disorders (01.01.2005)
Published in Movement disorders (01.01.2005)
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Journal Article
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations
Clark, Lorraine N., Afridi, Shehla, Mejia-Santana, Helen, Harris, Juliette, Louis, Elan D., Cote, Lucien J., Andrews, Howard, Singleton, Andrew, Wavrant De-Vrieze, Fabienne, Hardy, John, Mayeux, Richard, Fahn, Stanley, Waters, Cheryl, Ford, Blair, Frucht, Steven, Ottman, Ruth, Marder, Karen
Published in Movement disorders (01.07.2004)
Published in Movement disorders (01.07.2004)
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Journal Article
Increased rate of sporadic and recurrent rare genic copy number variants in Parkinson's disease among Ashkenazi Jews
Liu, Xinmin, Cheng, Rong, Ye, Xin, Verbitsky, Miguel, Kisselev, Sergey, Mejia‐Santana, Helen, Louis, Elan D., Cote, Lucien J., Andrews, Howard F., Waters, Cheryl H., Ford, Blair, Fahn, Stanley, Marder, Karen, Lee, Joseph H., Clark, Lorraine N.
Published in Molecular genetics & genomic medicine (01.09.2013)
Published in Molecular genetics & genomic medicine (01.09.2013)
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