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1

Polyoxometalate-Engineered Building Blocks with Gold Cores for the Self-Assembly of Responsive Water-Soluble Nanostructures

Wang, Yizhan, Raula, Manoj, Wang, Yifeng, Zeiri, Offer, Chakraborty, Sourav, Gan-Or, Gal, Gadot, Eyal, Weinstock, Ira A.

Journal:

Angewandte Chemie International Edition

Year:

2017

Language:

english

File:

PDF, 2.24 MB

english, 2017

2

Sleep disorders and Parkinson disease; lessons from genetics

Gan-Or, Ziv, Alcalay, Roy, Rouleau, Guy A., Postuma, Ronald B.

Journal:

Sleep Medicine Reviews

Year:

2018

Language:

english

File:

PDF, 1.25 MB

english, 2018

3

Design of an inherently-stable water oxidation catalyst

Chakraborty, Biswarup, Gan-Or, Gal, Raula, Manoj, Gadot, Eyal, Weinstock, Ira A.

Journal:

Nature Communications

Year:

2018

Language:

english

File:

PDF, 1.42 MB

english, 2018

4

Exposure to pesticides and welding hastens the age-at-onset of Parkinson’s disease

Gamache, Pierre-Luc, Salem, Ikhlass Haj, Roux-Dubois, Noémie, Le Bouthillier, Jacques, Gan-Or, Ziv, Dupré, Nicolas

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2019

Language:

english

File:

PDF, 1.04 MB

english, 2019

5

Ruxolitinib for Glucocorticoid-Refractory Acute Graft-versus-Host Disease

Zeiser, Robert, von Bubnoff, Nikolas, Butler, Jason, Mohty, Mohamad, Niederwieser, Dietger, Or, Reuven, Szer, Jeff, Wagner, Eva M., Zuckerman, Tsila, Mahuzier, BruyÃ¨re, Xu, Judith, Wilke, Celine, Gan

Journal:

New England Journal of Medicine

Year:

2020

File:

PDF, 615 KB

2020

6

Age at Onset of Parkinsonâs Disease Among Ashkenazi Jewish Patients: Contribution of Environmental Factors, LRRK2 p.G2019S and GBA p.N370S Mutations

Yahalom, Gilad, Rigbi, Amihai, Israeli-Korn, Simon, Krohn, Lynne, Rudakou, Uladzislau, Ruskey, Jennifer A., Benshimol, Lior, Tsafnat, Tal, Gan-Or, Ziv, Hassin-Baer, Sharon, Greenbaum, Lior

Journal:

Journal of Parkinson s Disease

Year:

2020

File:

PDF, 104 KB

2020

7

TheLRRK2G2019S mutation as the cause of Parkinson’s disease in Ashkenazi Jews

Avner Thaler, Elissa Ash, Ziv Gan-Or, Avi Orr-Urtreger, Nir Giladi

Journal:

Journal of Neural Transmission

Year:

2009

Language:

english

File:

PDF, 218 KB

english, 2009

8

LRRK2andGBAmutations differentially affect the initial presentation of Parkinson disease

Z. Gan-Or, A. Bar-Shira, A. Mirelman, T. Gurevich, M. Kedmi, N. Giladi, A. Orr-Urtreger

Journal:

Year:

2010

Language:

english

File:

PDF, 111 KB

english, 2010

9

Homozygosity for theMTX1c.184T>A (p.S63T) alteration modifies the age of onset inGBA-associated Parkinson's disease

Ziv Gan-Or, Anat Bar-Shira, Tanya Gurevich, Nir Giladi, Avi Orr-Urtreger

Journal:

Year:

2011

Language:

english

File:

PDF, 248 KB

english, 2011

10

The Age at Motor Symptoms Onset inLRRK2-Associated Parkinson's Disease is Affected by a Variation in theMAPTLocus: A Possible Interaction

Ziv Gan-Or, Anat Bar-Shira, Anat Mirelman, Tanya Gurevich, Nir Giladi, Avi Orr-Urtreger

Journal:

Journal of Molecular Neuroscience

Year:

2012

Language:

english

File:

PDF, 108 KB

english, 2012

11

Normal hematopoietic reconstitution following ASTA-Z 7557-purged grafts in the absence of in vitro CFU-GM colony growth

A. Nagler, M. Mumcuoglu, E. Naparstek, R. Or, S. Gan, S. Slavin

Journal:

Leukemia Research

Year:

1993

Language:

english

File:

PDF, 578 KB

english, 1993

12

False-positive results using a Gaucher diagnostic kit – RecTL and N370S

Jae Hyuk Choi, Arash Velayati, Barbara K. Stubblefield, Avi Orr-Urtreger, Ziv Gan-Or, Nahid Tayebi, Ellen Sidransky

Journal:

Molecular Genetics and Metabolism

Year:

2010

Language:

english

File:

PDF, 157 KB

english, 2010

13

2.114 PERIPAPILLARY RETINAL NERVE FIBER LAYER THICKNESS IN PATIENTS WITH PARKINSON'S DISEASE, PATIENTS WITH DIFFERENT GENETICS STATUS

T. Gurevich, H. Shabtai, E. Naftaliev, M. Neudorfer, Y. Balash, E. Rosenberg, A. Mirelman, J. Knaani, A. Bar Shira, Z. Gan Or, A. Orr-Urtreger, A. Kesler, N. Giladi

Journal:

Parkinsonism & Related Disorders

Year:

2012

Language:

english

File:

PDF, 58 KB

english, 2012

14

CHRNB3 c.-57A>G functional promoter change affects Parkinson's disease and smoking

Bar-Shira, Anat, Gana-Weisz, Mali, Gan-Or, Ziv, Giladi, Eytan, Giladi, Nir, Orr-Urtreger, Avi

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 489 KB

english, 2014

15

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

Wu, R.-M., Lin, C.-H., Lin, H.-I., Orr-Urtreger, A., Gan-Or, Z.

Journal:

Year:

2014

Language:

english

File:

PDF, 184 KB

english, 2014

16

Genetic markers of Restless Legs Syndrome in Parkinson disease

Gan-Or, Ziv, Alcalay, Roy N., Bar-Shira, Anat, Leblond, Claire S., Postuma, Ronald B., Ben-Shachar, Shay, Waters, Cheryl, Johnson, Amelie, Levy, Oren, Mirelman, Anat, Gana-Weisz, Mali, Dupré, Nicolas,

Journal:

Parkinsonism & Related Disorders

Year:

2015

Language:

english

File:

PDF, 246 KB

english, 2015

17

Polyoxometalate Complexes of Anatase-Titanium Dioxide Cores in Water

Raula, Manoj, Gan Or, Gal, Saganovich, Marina, Zeiri, Offer, Wang, Yifeng, Chierotti, Michele R., Gobetto, Roberto, Weinstock, Ira A.

Journal:

Angewandte Chemie International Edition

Year:

2015

Language:

english

File:

PDF, 1.23 MB

english, 2015

18

Differential effects of severe vs mild GBA mutations on Parkinson disease

Gan-Or, Z., Amshalom, I., Kilarski, L. L., Bar-Shira, A., Gana-Weisz, M., Mirelman, A., Marder, K., Bressman, S., Giladi, N., Orr-Urtreger, A.

Journal:

Year:

2015

Language:

english

File:

PDF, 308 KB

english, 2015

19

Parkinson’s Disease Genetic Loci in Rapid Eye Movement Sleep Behavior Disorder

Gan-Or, Z., Girard, S. L., Noreau, A., Leblond, C. S., Gagnon, J. F., Arnulf, I., Mirarchi, C., Dauvilliers, Y., Desautels, A., Mitterling, T., Cochen De Cock, V., Frauscher, B., Monaca, C., Hogl, B.,

Journal:

Journal of Molecular Neuroscience

Year:

2015

Language:

english

File:

PDF, 225 KB

english, 2015

20

A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly

Srour, M., Hamdan, F. F., Gan-Or, Z., Labuda, D., Nassif, C., Oskoui, M., Gana-Weisz, M., Orr-Urtreger, A., Rouleau, G.A., Michaud, J.L.

Journal:

Clinical Genetics

Year:

2015

Language:

english

File:

PDF, 759 KB

english, 2015

21

LRRK2 mutations in Parkinson disease; a sex effect or lack thereof? A meta-analysis

Gan-Or, Ziv, Leblond, Claire S., Mallett, Victoria, Orr-Urtreger, Avi, Dion, Patrick A., Rouleau, Guy A.

Journal:

Parkinsonism & Related Disorders

Year:

2015

Language:

english

File:

PDF, 1020 KB

english, 2015

22

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

Gan-Or, Z., Ozelius, L. J., Bar-Shira, A., Saunders-Pullman, R., Mirelman, A., Kornreich, R., Gana-Weisz, M., Raymond, D., Rozenkrantz, L., Deik, A., Gurevich, T., Gross, S. J., Schreiber-Agus, N., Gi

Journal:

Year:

2013

Language:

english

File:

PDF, 207 KB

english, 2013

23

Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset

Gan-Or, Z., Giladi, N., Rozovski, U., Shifrin, C., Rosner, S., Gurevich, T., Bar-Shira, A., Orr-Urtreger, A.

Journal:

Year:

2008

Language:

english

File:

PDF, 303 KB

english, 2008

24

Differential phenotype in Parkinson's disease patients with severe versus mild GBA mutations

Gan-Or, Z., Giladi, N., Orr-Urtreger, A.

Journal:

Year:

2009

Language:

english

File:

PDF, 69 KB

english, 2009

25

PARK16 haplotypes and the importance of protective genetic factors in Parkinson’s disease

Journal:

Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 117 KB

english, 2015

26

Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations

Alcalay, R. N., Levy, O. A., Waters, C. C., Fahn, S., Ford, B., Kuo, S.-H., Mazzoni, P., Pauciulo, M. W., Nichols, W. C., Gan-Or, Z., Rouleau, G. A., Chung, W. K., Wolf, P., Oliva, P., Keutzer, J., Ma

Journal:

Year:

2015

Language:

english

File:

PDF, 381 KB

english, 2015

27

Genetic perspective on the role of the Autophagy-Lysosome Pathway in Parkinson disease

Gan-Or, Ziv, Dion, Patrick A., Rouleau, Guy A.

Journal:

Year:

2015

Language:

english

File:

PDF, 1.09 MB

english, 2015

28

Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndrome

Gan-Or, Ziv, Zhou, Sirui, Ambalavanan, Amirthagowri, Leblond, Claire S., Xie, Pingxing, Johnson, Amelie, Spiegelman, Dan, Allen, Richard P., Earley, Christopher J., Desautels, Alex, Montplaisir, Jacqu

Journal:

Year:

2015

Language:

english

File:

PDF, 587 KB

english, 2015

29

The emerging role of SMPD1 mutations in Parkinson’s disease; implications for future studies

Gan-Or, Ziv, Orr-Urtreger, Avi, Alcalay, Roy N., Bressman, Susan, Giladi, Nir, Rouleau, Guy A.

Journal:

Parkinsonism & Related Disorders

Year:

2015

Language:

english

File:

PDF, 323 KB

english, 2015

30

The Alzheimer diseaseBIN1locus as a modifier ofGBA-associated Parkinson disease

Gan-Or, Z., Amshalom, I., Bar-Shira, A., Gana-Weisz, M., Mirelman, A., Marder, K., Bressman, S., Giladi, N., Orr-Urtreger, A.

Journal:

Journal of Neurology

Year:

2015

Language:

english

File:

PDF, 475 KB

english, 2015

31

Down-regulation of B cell-related genes in peripheral blood leukocytes of Parkinson's disease patients with and without GBA mutations

Kobo, Hila, Bar-Shira, Anat, Dahary, Dvir, Gan-Or, Ziv, Mirelman, Anat, Goldstein, Orly, Giladi, Nir, Orr-Urtreger, Avi

Journal:

Molecular Genetics and Metabolism

Year:

2015

Language:

english

File:

PDF, 392 KB

english, 2015

32

Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis

Leblond, Claire S., Gan-Or, Ziv, Spiegelman, Dan, Laurent, Sandra B., Szuto, Anna, Hodgkinson, Alan, Dionne-Laporte, Alexandre, Provencher, Pierre, de Carvalho, Mamede, Orrù, Sandro, Brunet, Denis, Bo

Journal:

Neurobiology of Aging

Year:

2015

Language:

english

File:

PDF, 793 KB

english, 2015

33

GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder

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., S

Journal:

Annals of Clinical and Translational Neurology

Year:

2015

Language:

english

File:

PDF, 92 KB

english, 2015

34

SEPT14Is Associated with a Reduced Risk for Parkinson’s Disease and Expressed in Human Brain

Rozenkrantz, Liron, Gan-Or, Ziv, Gana-Weisz, Mali, Mirelman, Anat, Giladi, Nir, Bar-Shira, Anat, Orr-Urtreger, Avi

Journal:

Journal of Molecular Neuroscience

Year:

2016

Language:

english

File:

PDF, 384 KB

english, 2016

35

De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopia

Leblond, C. S., Webber, A., Gan-Or, Z., Moore, F., Dagher, A., Dion, P. A., Rouleau, G. A.

Journal:

Neurology: Genetics

Year:

2016

Language:

english

File:

PDF, 394 KB

english, 2016

36

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Gan-Or, Ziv, Bouslam, Naima, Birouk, Nazha, Lissouba, Alexandra, Chambers, Daniel B., Vérièpe, Julie, Androschuck, Alaura, Laurent, Sandra B., Rochefort, Daniel, Spiegelman, Dan, Dionne-Laporte, Alexa

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.68 MB

english, 2016

37

The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder

Gan-Or, Ziv, Mohsin, Noreen, Girard, Simon L., Montplaisir, Jacques Y., Ambalavanan, Amirthagowri, Strong, Stephanie, Mallett, Victoria, Laurent, Sandra B., Bourassa, Cynthia V., Boivin, Michel, Langl

Journal:

Neurobiology of Aging

Year:

2016

Language:

english

File:

PDF, 787 KB

english, 2016

38

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Gan-Or, Ziv, Bouslam, Naima, Birouk, Nazha, Lissouba, Alexandra, Chambers, Daniel B., Vérièpe, Julie, Androschuk, Alaura, Laurent, Sandra B., Rochefort, Daniel, Spiegelman, Dan, Dionne-Laporte, Alexan

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 55 KB

english, 2016

39

Association of Sequence Alterations in the Putative Promoter of RAB7L1 With a Reduced Parkinson Disease Risk

Journal:

Archives of Neurology

Year:

2012

Language:

english

File:

PDF, 174 KB

english, 2012

40

Case-Control and Family-Based Association Study of Specific PTPRD Variants in Restless Legs Syndrome

Gan-Or, Ziv, Zhou, Sirui, Johnson, Amelie, Montplaisir, Jacques Y., Allen, Richard P., Earley, Christopher J., Desautels, Alex, Dion, Patrick A., Xiong, Lan, Rouleau, Guy A.

Journal:

Movement Disorders Clinical Practice

Year:

2016

Language:

english

File:

PDF, 121 KB

english, 2016

41

Polyoxometalate Complexes of Anatase-Titanium Dioxide Cores in Water

Raula, Manoj, Gan Or, Gal, Saganovich, Marina, Zeiri, Offer, Wang, Yifeng, Chierotti, Michele R., Gobetto, Roberto, Weinstock, Ira A.

Journal:

Angewandte Chemie

Year:

2015

Language:

english

File:

PDF, 1.45 MB

english, 2015

42

Tinea capitis outbreak among paediatric refugee population, an evolving healthcare challenge

Mashiah, Jacob, Kutz, Ana, Ben Ami, Ronen, Savion, Mihal, Goldberg, Ilan, Gan Or, Tamar, Zidan, Omri, Sprecher, Eli, Harel, Avikam

Journal:

Year:

2016

Language:

english

File:

PDF, 100 KB

english, 2016

43

A Randomized Controlled Multicenter Study Comparing Recombinant Interleukin 2 (rIL-2) in Conjunction With Recombinant Interferon Alpha (IFN-α) Versus no Immunotherapy for Patients With Malignant Lymphoma Postautologous Stem Cell Transplantation

Nagler, Arnon, Berger, Raanan, Ackerstein, Aliza, Czyz, Jaroslaw A., Diez-Martin, Jose Luis, Naparstek, Elizabeth, Or, Reuven, Gan, Shlomit, Shimoni, Avichai, Slavin, Shimon

Journal:

Journal of Immunotherapy

Year:

2010

Language:

english

File:

PDF, 241 KB

english, 2010

44

Calpain 1 in neurodegeneration: a therapeutic target?

Gan-Or, Ziv, Rouleau, Guy A

Journal:

The Lancet Neurology

Year:

2016

Language:

english

File:

PDF, 38 KB

english, 2016

45

A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia

Diomedi, Marina, Gan-Or, Ziv, Placidi, Fabio, Dion, Patrick A., Szuto, Anna, Bengala, Mario, Rouleau, Guy A., Gigli, Gian Luigi

Journal:

European Journal of Medical Genetics

Year:

2016

Language:

english

File:

PDF, 1.00 MB

english, 2016

46

RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population

Zhou, Sirui, Ambalavanan, Amirthagowri, Rochefort, Daniel, Xie, Pingxing, Bourassa, Cynthia V., Hince, Pascale, Dionne-Laporte, Alexandre, Spiegelman, Dan, Gan-Or, Ziv, Mirarchi, Cathy, Zaharieva, Ves

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.16 MB

english, 2016

47

The dementia-associated APOE ε4 allele is not associated with REM sleep behavior disorder

Gan-Or, Ziv, Montplaisir, Jacques Y., Ross, Jay P., Poirier, Judes, Warby, Simon C., Arnulf, Isabelle, Strong, Stephanie, Dauvilliers, Yves, Leblond, Claire S., Hu, Michele T.M., Högl, Birgit, Stefani

Journal:

Neurobiology of Aging

Year:

2016

File:

PDF, 286 KB

2016

48

Dynamics of microtubules and their associated proteins: Recent insights and clinical implicationsAuthor Response

Gan-Or, Ziv, Benarroch, Eduardo E., Rouleau, Guy A.

Journal:

Year:

2016

Language:

english

File:

PDF, 176 KB

english, 2016

49

Clinical and genetic study of hereditary spastic paraplegia in Canada

Chrestian, Nicolas, Dupré, Nicolas, Gan-Or, Ziv, Szuto, Anna, Chen, Shiyi, Venkitachalam, Anil, Brisson, Jean-Denis, Warman-Chardon, Jodi, Ahmed, Sohnee, Ashtiani, Setareh, MacDonald, Heather, Mohsin,

Journal:

Neurology: Genetics

Year:

2017

Language:

english

File:

PDF, 538 KB

english, 2017

50

KCNA2 mutations are rare in hereditary spastic paraplegia

Gan-Or, Ziv, Yoon, Grace, Suchowersky, Oksana, Dupré, Nicolas, Rouleau, Guy A.

Journal:

Annals of Neurology

Year:

2017

Language:

english

File:

PDF, 593 KB

english, 2017