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Reference EntriesFull Text
Bressman, Susan B
Journal title:American Men & Women of Science : A Biographical Directory of Today’s Leaders in Physical, Biological and Related Sciences: BAY-BUP, 2022, p.1354-1355
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ArticlesPeer ReviewedFull Text
Digitized Spiral Drawing: A Possible Biomarker for Early Parkinson’s Disease
Author / Creator:San Luciano, Marta ; Wang, Cuiling ; Ortega, Roberto A. ; Yu, Qiping ; Boschung, Sarah ; Soto-Valencia, Jeannie ; Bressman, Susan B. ; Lipton, Richard B. ; Pullman, Seth ; Saunders-Pullman, Rachel
Publisher:United States: Public Library of Science
Journal title:PloS one, 2016-10, Vol.11 (10), p.e0162799
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ArticlesPeer ReviewedFull Text
Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia
Author / Creator:Fuchs, Tania ; Gavarini, Sophie ; Saunders-Pullman, Rachel ; Raymond, Deborah ; Ehrlich, Michelle E ; Bressman, Susan B ; Ozelius, Laurie J
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2009-03, Vol.41 (3), p.286-288
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ArticlesPeer ReviewedFull Text
Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study
Author / Creator:Bressman, Susan B, MD ; Raymond, Deborah, MS ; Fuchs, Tania, PhD ; Heiman, Gary A, PhD ; Ozelius, Laurie J, PhD ; Saunders-Pullman, Rachel, MD
Publisher:England: Elsevier Limited
Journal title:Lancet neurology, 2009-05, Vol.8 (5), p.441-446
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ArticlesPeer ReviewedFull Text
Pallidal Deep Brain Stimulation for Primary Dystonia in Children
Author / Creator:Haridas, Abilash ; Tagliati, Michele ; Osborn, Irene ; Isaias, Ioannis ; Gologorsky, Yakov ; Bressman, Susan B ; Weisz, Donald ; Alterman, Ron L
Publisher:Hagerstown, MD: Oxford University Press
Journal title:Neurosurgery, 2011-03, Vol.68 (3), p.738-743
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ArticlesPeer ReviewedFull Text
DYT1 dystonia increases risk taking in humans
Author / Creator:Arkadir, David ; Radulescu, Angela ; Raymond, Deborah ; Lubarr, Naomi ; Bressman, Susan B ; Mazzoni, Pietro ; Niv, Yael
Publisher:England: eLife Sciences Publications Ltd
Journal title:eLife, 2016-06, Vol.5
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ArticlesPeer ReviewedFull Text
Genetic risk variants in New Yorkers of Puerto Rican and Dominican Republic heritage with Parkinson’s disease
Author / Creator:Miltenberger-Miltenyi, Gabriel ; Ortega, Roberto A. ; Domingo, Aloysius ; Yadav, Rachita ; Nishiyama, Ayumi ; Raymond, Deborah ; Katsnelson, Viktoriya ; Urval, Nikita ; Swan, Matthew ; Shanker, Vicki ; Miravite, Joan ; Walker, Ruth H. ; Bressman, Susan B. ; Ozelius, Laurie J. ; Cabassa, José C. ; Saunders-Pullman, Rachel
Publisher:London: Nature Publishing Group UK
Journal title:NPJ Parkinson's Disease, 2023-12, Vol.9 (1), p.160-160, Article 160
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ArticlesPeer ReviewedFull Text
Mutations in GNAL cause primary torsion dystonia
Author / Creator:Fuchs, Tania ; Saunders-Pullman, Rachel ; Masuho, Ikuo ; Luciano, Marta San ; Raymond, Deborah ; Factor, Stewart ; Lang, Anthony E ; Liang, Tsao-Wei ; Trosch, Richard M ; White, Sierra ; Ainehsazan, Edmond ; Hervé, Denis ; Sharma, Nutan ; Ehrlich, Michelle E ; Martemyanov, Kirill A ; Bressman, Susan B ; Ozelius, Laurie J
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2013-01, Vol.45 (1), p.88-92
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ArticlesPeer ReviewedFull Text
The diagnosis of dystonia
Author / Creator:Geyer, Howard L ; Bressman, Susan B
Publisher:England: Elsevier Ltd
Journal title:Lancet neurology, 2006-09, Vol.5 (9), p.780-790
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ArticlesPeer ReviewedFull Text
Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression
Author / Creator:Ortega, Roberto A. ; Wang, Cuiling ; Raymond, Deborah ; Bryant, Nicole ; Scherzer, Clemens R. ; Thaler, Avner ; Alcalay, Roy N. ; West, Andrew B. ; Mirelman, Anat ; Kuras, Yuliya ; Marder, Karen S. ; Giladi, Nir ; Ozelius, Laurie J. ; Bressman, Susan B. ; Saunders-Pullman, Rachel
Publisher:United States: American Medical Association
Journal title:JAMA network open, 2021-04, Vol.4 (4), p.e215845-e215845
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ArticlesPeer ReviewedFull Text
LRRK2 G2019S as a Cause of Parkinson's Disease in Ashkenazi Jews
Author / Creator:Klein, Christine ; Risch, Neil ; Ozelius, Laurie J ; Bressman, Susan B ; Henick, Brian ; Soto-Valencia, Jeannie ; Saunders-Pullman, Rachel ; Hailpern, Susan M ; Ohmann, Erin ; Senthil, Geetha ; Lipton, Richard B ; Deligtisch, Amanda ; Tagliati, Michele ; Hunt, Ann L
Publisher:United States: Massachusetts Medical Society
Journal title:The New England journal of medicine, 2006-01, Vol.354 (4), p.424-425
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ArticlesPeer ReviewedFull Text
Pallidal deep brain stimulation for DYT6 dystonia
Author / Creator:Panov, Fedor ; Tagliati, Michele ; Ozelius, Laurie J ; Fuchs, Tania ; Gologorsky, Yakov ; Cheung, Tyler ; Avshalumov, Marat ; Bressman, Susan B ; Saunders-Pullman, Rachel ; Weisz, Donald ; Alterman, Ron L
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of neurology, neurosurgery and psychiatry, 2012-02, Vol.83 (2), p.182-187
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ArticlesPeer ReviewedFull Text
Evidence for increased completed suicide in first-degree relatives of LRRK2 G2019S mutation Parkinson’s disease
Author / Creator:Ortega, Roberto Angel ; Groves, Mark ; Mirelman, Anat ; Alcalay, Roy N ; Raymond, Deborah ; Elango, Sonya ; Mejia-Santana, Helen ; Giladi, Nir ; Marder, Karen ; Bressman, Susan B ; Saunders-Pullman, Rachel
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of neurology, neurosurgery and psychiatry, 2019-07, Vol.90 (7), p.843-844
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ArticlesPeer ReviewedFull Text
GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder
Author / Creator:Gan‐Or, Ziv ; Mirelman, Anat ; Postuma, Ronald B. ; Arnulf, Isabelle ; Bar‐Shira, Anat ; Dauvilliers, Yves ; Desautels, Alex ; Gagnon, Jean‐François ; Leblond, Claire S. ; Frauscher, Birgit ; Alcalay, Roy N. ; Saunders‐Pullman, Rachel ; Bressman, Susan B. ; Marder, Karen ; Monaca, Christelle ; Högl, Birgit ; Orr‐Urtreger, Avi ; Dion, Patrick A. ; Montplaisir, Jacques Y. ; Giladi, Nir ; Rouleau, Guy A.
Publisher:United States: John Wiley & Sons, Inc
Journal title:Annals of clinical and translational neurology, 2015-09, Vol.2 (9), p.941-945
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Newspaper ArticlesFull Text
THE NATION; Genetic Link to Parkinson's Disease Is Detected in 2 Ethnic Groups; Scientists say a mutation causes 18% of cases in Ashkenazi Jews and 37% in North African Arabs: HOME EDITION
Author / Creator:Maugh, Thomas H
Publisher:Los Angeles, Calif: Los Angeles Times Communications LLC
Journal title:The Los Angeles times, 2006-01-26
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ArticlesPeer ReviewedFull Text
What’s new in dystonia?
Author / Creator:Shanker, Vicki ; Bressman, Susan B.
Publisher:New York: Current Science Inc
Journal title:Current neurology and neuroscience reports, 2009-07, Vol.9 (4), p.278-284
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ArticlesPeer ReviewedFull Text
Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?
Author / Creator: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.
Publisher:United States: BlackWell Publishing Ltd
Journal title:Annals of clinical and translational neurology, 2014-09, Vol.1 (9), p.670-678
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ArticlesPeer ReviewedFull Text
Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonism
Author / Creator:Leung, Joanne ; Klein, Christine ; Friedman, Jennifer ; Vieregge, Peter ; Jacobs, Helfried ; Doheny, Dana ; Kamm, Christoph ; DeLeon, Deborah ; Pramstaller, Peter P. ; Penney, John B. ; Eisengart, Marvin ; Jankovic, Joseph ; Gasser, Thomas ; Bressman, Susan B. ; Corey, David P. ; Kramer, Patricia ; Brin, Mitchell F. ; Ozelius, Laurie J. ; Breakefield, Xandra O.
Publisher:Berlin: Springer
Journal title:Neurogenetics, 2001-07, Vol.3 (3), p.133-143
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ArticlesPeer ReviewedFull Text
Olfactory identification in LRRK 2 G2019S mutation carriers: a relevant marker?
Author / Creator: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.
Publisher:Bognor Regis: John Wiley & Sons, Inc
Journal title:Annals of clinical and translational neurology, 2014-09, Vol.1 (9), p.670-678
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ArticlesPeer ReviewedFull Text
Spatial Discrimination Threshold Abnormalities are not Detected in a Pilot Study of DYT6 Dystonia Mutation Carriers
Author / Creator:Deik, Andres F. ; O’Riordan, Sean ; San Luciano, Marta ; Shanker, Vicki L. ; Raymond, Deborah ; Bressman, Susan B. ; Saunders-Pullman, Rachel
Publisher:Dallas: Ubiquity Press
Journal title:Tremor and other hyperkinetic movements (New York, N.Y.), 2012-01, Vol.2, p.2
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Bressman, Susan B

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Digitized Spiral Drawing: A Possible Biomarker for Early Parkinson’s Disease

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Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia

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Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study

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Pallidal Deep Brain Stimulation for Primary Dystonia in Children

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DYT1 dystonia increases risk taking in humans

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Genetic risk variants in New Yorkers of Puerto Rican and Dominican Republic heritage with Parkinson’s disease

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Mutations in GNAL cause primary torsion dystonia

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The diagnosis of dystonia

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Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression

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LRRK2 G2019S as a Cause of Parkinson's Disease in Ashkenazi Jews

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Pallidal deep brain stimulation for DYT6 dystonia

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Evidence for increased completed suicide in first-degree relatives of LRRK2 G2019S mutation Parkinson’s disease

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GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder

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THE NATION; Genetic Link to Parkinson's Disease Is Detected in 2 Ethnic Groups; Scientists say a mutation causes 18% of cases in Ashkenazi Jews and 37% in North African Arabs: HOME EDITION

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What’s new in dystonia?

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Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?

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Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonism

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Olfactory identification in LRRK 2 G2019S mutation carriers: a relevant marker?

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Spatial Discrimination Threshold Abnormalities are not Detected in a Pilot Study of DYT6 Dystonia Mutation Carriers

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