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1

Antioxidant Effects of Curcumin in Models of Neurodegeneration, Ageing, Oxidative and NITROSATIVE Stress: A Review

Abrahams, Shameemah, Haylett, William L., Johnson, Glynis, Carr, Jonathan A., Bardien, Soraya

Journal:

Year:

2019

Language:

english

File:

PDF, 1.78 MB

english, 2019

2

The prevalence and genetics of Parkinson's disease in sub-Saharan Africans

Blanckenberg, Janine, Bardien, Soraya, Glanzmann, Brigitte, Okubadejo, Njideka U., Carr, Jonathan A.

Journal:

Journal of the Neurological Sciences

Year:

2013

Language:

english

File:

PDF, 143 KB

english, 2013

3

A systematic review of genetic variants associated with metabolic syndrome in patients with schizophrenia

Malan-Müller, Stefanie, Kilian, Sanja, van den Heuvel, Leigh L., Bardien, Soraya, Asmal, Laila, Warnich, Louise, Emsley, Robin A., Hemmings, Sîan M.J., Seedat, Soraya

Journal:

Schizophrenia Research

Year:

2015

Language:

english

File:

PDF, 975 KB

english, 2015

4

A review of genome-wide transcriptomics studies in Parkinson's disease

Borrageiro, Genevie, Haylett, William, Seedat, Soraya, Kuivaniemi, Helena, Bardien, Soraya

Journal:

European Journal of Neuroscience

Year:

2017

Language:

english

File:

PDF, 4.94 MB

english, 2017

5

Parkinson's disease in Nigeria: A review of published studies and recommendations for future research

Oluwole, Oluwafemi G., Kuivaniemi, Helena, Carr, Jonathan A., Ross, Owen A., Olaogun, Matthew O.B., Bardien, Soraya, Komolafe, Morenikeji A.

Journal:

Parkinsonism & Related Disorders

Year:

2018

Language:

english

File:

PDF, 570 KB

english, 2018

6

Rhodopsin mutation G109R in a family with autosomal dominant retinitis pigmentosa

Rene Goliath, Soraya Bardien, Alison September, Rebecca Martin, Rajkumar Ramesar, Jacquie Greenberg

Journal:

Year:

1998

Language:

english

File:

PDF, 149 KB

english, 1998

7

A South African mixed ancestry family with Huntington disease-like 2: Clinical and genetic features

Soraya Bardien, Fatima Abrahams, Himla Soodyall, Lize van der Merwe, Jacquie Greenberg, Tinus Brink, Jonathan Carr

Journal:

Movement Disorders

Year:

2007

Language:

english

File:

PDF, 209 KB

english, 2007

8

Identification of a novel functional deletion variant in the 5'-UTR of the DJ-1 gene

Rowena J Keyser, Lize van der Merwe, Mauritz Venter, Craig Kinnear, Louise Warnich, Jonathan Carr, Soraya Bardien

Journal:

BMC Medical Genetics

Year:

2009

Language:

english

File:

PDF, 1.93 MB

english, 2009

9

A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness

Soraya Bardien, Hannique Human, Tashneem Harris, Gwynneth Hefke, Rene Veikondis, H Simon Schaaf, Lize van der Merwe, John H Greinwald, Johan Fagan, Greetje de Jong

Journal:

BMC Medical Genetics

Year:

2009

Language:

english

File:

PDF, 819 KB

english, 2009

10

Arrhythmogenic right ventricular cardiomyopathy type 6 (ARVC6): support for the locus assignment, narrowing of the critical region and mutation screening of three candidate genes

Luzuko O Matolweni, Soraya Bardien, George Rebello, Ekow Oppon, Miroslav Munclinger, Rajkumar Ramesar, Hugh Watkins, Bongani M Mayosi

Journal:

BMC Medical Genetics

Year:

2006

Language:

english

File:

PDF, 532 KB

english, 2006

11

Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South African families

R. S. Ramesar, Soraya Bardien, Peter Beighton, Alan Bryer

Journal:

Year:

1997

Language:

english

File:

PDF, 89 KB

english, 1997

12

Retinitis pigmentosa locus on 17q (RP17): fine localization to 17q22 and exclusion of thePDEGandTIMP2genes

Soraya Bardien, Rajkumar Ramesar, Shomi Bhattacharya, J. Greenberg

Journal:

Year:

1997

Language:

english

File:

PDF, 97 KB

english, 1997

13

LRRK2G2019S mutation: frequency and haplotype data in South African Parkinson’s disease patients

Soraya Bardien, Angelica Marsberg, Rowena Keyser, Debbie Lombard, Suzanne Lesage, Alexis Brice, Jonathan Carr

Journal:

Journal of Neural Transmission

Year:

2010

Language:

english

File:

PDF, 270 KB

english, 2010

14

Identification of Parkinson’s disease candidate genes using CAESAR and screening ofMAPTandSNCAIPin South African Parkinson’s disease patients

Rowena J. Keyser, Ekow Oppon, Jonathan A. Carr, Soraya Bardien

Journal:

Journal of Neural Transmission

Year:

2011

Language:

english

File:

PDF, 219 KB

english, 2011

15

Analysis of exon dosage using MLPA in South African Parkinson's disease patients

Rowena J. Keyser, Debbie Lombard, Rene Veikondis, Jonathan Carr, Soraya Bardien

Journal:

Year:

2010

Language:

english

File:

PDF, 507 KB

english, 2010

16

Novel non-sense GCH1 mutation in a South African family diagnosed with dopa-responsive dystonia

S. Bardien, R. Keyser, D. Lombard, M. Du Plessis, H. Human, J. Carr

Journal:

European Journal of Neurology

Year:

2010

Language:

english

File:

PDF, 217 KB

english, 2010

17

Refinement of the RP17 locus for autosomal dominant retinitis pigmentosa, construction of a YAC contig and investigation of the candidate gene retinal fascin

Bardien-Kruger, Soraya, Greenberg, Jacquie, Tubb, Benjamin, Bryan, Joseph, Queimado, Lurdes, Lovett, Michael, Ramesar, Rajkumar S

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 154 KB

english, 1999

18

Synergistic Effects of HIV in Aminoglycoside Ototoxicity

Johannes Fagan, Soraya Bardien

Journal:

Otolaryngology - Head and Neck Surgery

Year:

2010

Language:

english

File:

PDF, 43 KB

english, 2010

19

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

Owen A Ross, Alexandra I Soto-Ortolaza, Michael G Heckman, Jan O Aasly, Nadine Abahuni, Grazia Annesi, Justin A Bacon, Soraya Bardien, Maria Bozi, Alexis Brice, Laura Brighina, Christine Van Broeckhov

Journal:

The Lancet Neurology

Year:

2011

Language:

english

File:

PDF, 271 KB

english, 2011

20

Acceptability of Stem Cell Therapy by Pregnant Women

Ryan J. Hodges, Nadia Bardien, Euan Wallace

Journal:

Year:

2012

Language:

english

File:

PDF, 208 KB

english, 2012

21

Characterization of Human Retinal Fascin Gene (FSCN2) at 17q25: Close Physical Linkage of Fascin and Cytoplasmic Actin Genes

Benjamin E. Tubb, Soraya Bardien-Kruger, Catherine D. Kashork, Lisa G. Shaffer, Louis S. Ramagli, Jingping Xu, Michael J. Siciliano, Joseph Bryan

Journal:

Year:

2000

Language:

english

File:

PDF, 440 KB

english, 2000

22

3231 Frequencies of different forms of autosomal dominant retinitis pigmentosa and a new locus for adRP

C.F. Inglehearn, S. Bardien, E.E. Tarttelin, J. Greenberg, M. Al-Maghtheh, N. Ebenezer, T.J. Keen, M. Jay, A.C. Bird, S.S. Bhattacharya

Journal:

Vision Research

Year:

1995

Language:

english

File:

PDF, 125 KB

english, 1995

23

A South African family with the mitochondrial A1555G mutation on haplogroup L0d

H. Human, D. Lombard, G. de Jong, S. Bardien

Journal:

Biochemical and Biophysical Research Communications

Year:

2009

Language:

english

File:

PDF, 310 KB

english, 2009

24

Investigation of mitochondrial sequence variants associated with aminoglycoside-induced ototoxicity in South African TB patients on aminoglycosides

Hanniqué Human, Christian M. Hagen, Greetje de Jong, Tashneem Harris, Debbie Lombard, Michael Christiansen, Soraya Bardien

Journal:

Biochemical and Biophysical Research Communications

Year:

2010

Language:

english

File:

PDF, 286 KB

english, 2010

25

Assessing the prevalence of PINK1 genetic variants in South African patients diagnosed with early- and late-onset Parkinson’s disease

Rowena J. Keyser, Suzanne Lesage, Alexis Brice, Jonathan Carr, Soraya Bardien

Journal:

Biochemical and Biophysical Research Communications

Year:

2010

Language:

english

File:

PDF, 333 KB

english, 2010

26

Molecular analysis of the parkin gene in South African patients diagnosed with Parkinson's disease

Soraya Bardien, Rowena Keyser, Yandiswa Yako, Debbie Lombard, Jonathan Carr

Journal:

Parkinsonism & Related Disorders

Year:

2009

Language:

english

File:

PDF, 160 KB

english, 2009

27

Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson’s disease

Soraya Bardien, Suzanne Lesage, Alexis Brice, Jonathan Carr

Journal:

Parkinsonism & Related Disorders

Year:

2011

Language:

english

File:

PDF, 497 KB

english, 2011

28

Mutations in the parkin gene are a minor cause of Parkinson's disease in the South African population

William L. Haylett, Rowena J. Keyser, Melissa C. du Plessis, Celia van der Merwe, Janine Blanckenberg, Debbie Lombard, Jonathan Carr, Soraya Bardien

Journal:

Parkinsonism & Related Disorders

Year:

2012

Language:

english

File:

PDF, 349 KB

english, 2012

29

Characterization of the human diacylglycerol kinase ε gene and its assessment as a candidate for inherited retinitis pigmentosa

Wen Tang, Soraya Bardien, Shomi S. Bhattacharya, Stephen M. Prescott

Journal:

Year:

1999

Language:

english

File:

PDF, 277 KB

english, 1999

30

Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium

Heckman, Michael G., Soto-Ortolaza, Alexandra I., Aasly, Jan O., Abahuni, Nadine, Annesi, Grazia, Bacon, Justin A., Bardien, Soraya, Bozi, Maria, Brice, Alexis, Brighina, Laura, Carr, Jonathan, Charti

Journal:

Movement Disorders

Year:

2013

Language:

english

File:

PDF, 231 KB

english, 2013

31

The broad-host-range plasmid pTF-FC2 requires a primase-like protein for autonomous replication in Escherichia coli

Dorrington, Rosemary A., Bardien, Soraya, Rawlings, Douglas E.

Journal:

Year:

1991

Language:

english

File:

PDF, 846 KB

english, 1991

32

Screening of two indel polymorphisms in the 5′UTR of theDJ-1gene in South African Parkinson’s disease patients

Glanzmann, Brigitte, Lombard, Debbie, Carr, Jonathan, Bardien, Soraya

Journal:

Journal of Neural Transmission

Year:

2014

Language:

english

File:

PDF, 284 KB

english, 2014

33

EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South Africa

Blanckenberg, Janine, Ntsapi, Claudia, Carr, Jonathan A., Bardien, Soraya

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 152 KB

english, 2014

34

Mitochondrial impairment observed in fibroblasts from South African Parkinson’s disease patients with parkin mutations

van der Merwe, Celia, Loos, Ben, Swart, Chrisna, Kinnear, Craig, Henning, Franclo, van der Merwe, Lize, Pillay, Komala, Muller, Nolan, Zaharie, Dan, Engelbrecht, Lize, Carr, Jonathan, Bardien, Soraya

Journal:

Biochemical and Biophysical Research Communications

Year:

2014

Language:

english

File:

PDF, 1.48 MB

english, 2014

35

The Frequency of the H402 Allele of CFH and Its Involvement with Age-Related Maculopathy in an Aged Black African Xhosa Population

Ziskind, Ari, Bardien, Soraya, van der Merwe, Lize, Webster, Andrew R.

Journal:

Ophthalmic Genetics

Year:

2008

Language:

english

File:

PDF, 63 KB

english, 2008

36

A study of meningiomas in South Africa: Investigating a correlation between clinical presentation, histopathology and genetic markers

Vivier, Johannes, Bardien, Soraya, Van der Merwe, Lize, Brusnicky, Jeanette, Zaharie, Dan, Keyser, Rowena, Hewlett, Richard, de Jong, Greetje, Hartzenberg, Bennie

Journal:

British Journal of Neurosurgery

Year:

2009

Language:

english

File:

PDF, 128 KB

english, 2009

37

Neurodegenerative disorders: Dysregulation of a carefully maintained balance?

Swart, Chrisna, Haylett, William, Kinnear, Craig, Johnson, Glynis, Bardien, Soraya, Loos, Ben

Journal:

Experimental Gerontology

Year:

2014

Language:

english

File:

PDF, 991 KB

english, 2014

38

Evidence for a common biological pathway linking three Parkinson's disease-causing genes: parkin , PINK1 and DJ-1

van der Merwe, Celia, Jalali Sefid Dashti, Zahra, Christoffels, Alan, Loos, Ben, Bardien, Soraya

Journal:

European Journal of Neuroscience

Year:

2015

Language:

english

File:

PDF, 651 KB

english, 2015

39

Apoptosis-inducing signal sequence mutation in carbonic anhydrase IV identified in patients with the RP17 form of retinitis pigmentosa

Rebello, G., Ramesar, R., Vorster, A., Roberts, L., Ehrenreich, L., Oppon, E., Gama, D., Bardien, S., Greenberg, J., Bonapace, G., Waheed, A., Shah, G. N., Sly, W. S.

Journal:

Proceedings of the National Academy of Sciences

Year:

2004

Language:

english

File:

PDF, 567 KB

english, 2004

40

Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity.

Ramesar, R S, Greenberg, J, Martin, R, Goliath, R, Bardien, S, Mundlos, S, Beighton, P

Journal:

Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 991 KB

english, 1996

41

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

Lesage, S., Patin, E., Condroyer, C., Leutenegger, A. L., Lohmann, E., Giladi, N., Bar-Shira, A., Belarbi, S., Hecham, N., Pollak, P., Ouvrard-Hernandez, A. M., Bardien, S., Carr, J., Benhassine, T.,

Journal:

Human Molecular Genetics

Year:

2010

Language:

english

File:

PDF, 165 KB

english, 2010

42

Novel LRRK2 mutations in Parkinsonism

Trinh, Joanne, Guella, Ilaria, McKenzie, Marna, Gustavsson, Emil K., Szu-Tu, Chelsea, Petersen, Maria Skaalum, Rajput, Alex, Rajput, Ali H., McKeown, Martin, Jeon, Beom S., Aasly, Jan O., Bardien, Sor

Journal:

Parkinsonism & Related Disorders

Year:

2015

Language:

english

File:

PDF, 170 KB

english, 2015

43

Large-scale assessment of polyglutamine repeat expansions in Parkinson disease

Wang, L., Aasly, J. O., Annesi, G., Bardien, S., Bozi, M., Brice, A., Carr, J., Chung, S. J., Clarke, C., Crosiers, D., Deutschlander, A., Eckstein, G., Farrer, M. J., Goldwurm, S., Garraux, G., Hadji

Journal:

Year:

2015

Language:

english

File:

PDF, 474 KB

english, 2015

44

Characterisation of the human voltage-gated potassium channel gene, KCNA7, a candidate gene for inherited cardiac disorders, and its exclusion as cause of progressive familial heart block I (PFHBI)

Bardien-Kruger, Soraya, Wulff, Heike, Arieff, Zainu, Brink, Paul, Chandy, K George, Corfield, Valerie

Journal:

European Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 242 KB

english, 2002

45

Exonic rearrangements in the known Parkinson’s disease-causing genes are a rare cause of the disease in South African patients

van der Merwe, Celia, Carr, Jonathan, Glanzmann, Brigitte, Bardien, Soraya

Journal:

Neuroscience Letters

Year:

2016

Language:

english

File:

PDF, 992 KB

english, 2016

46

Curcumin Rescues a PINK1 Knock Down SH-SY5Y Cellular Model of Parkinson’s Disease from Mitochondrial Dysfunction and Cell Death

van der Merwe, Celia, van Dyk, Hayley Christy, Engelbrecht, Lize, van der Westhuizen, Francois Hendrikus, Kinnear, Craig, Loos, Ben, Bardien, Soraya

Journal:

Molecular Neurobiology

Year:

2017

Language:

english

File:

PDF, 942 KB

english, 2017

47

Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients

Bardien, Soraya, Blanckenberg, Janine, van der Merwe, Lize, Farrer, Matthew J., Ross, Owen A.

Journal:

Movement Disorders

Year:

2013

Language:

english

File:

PDF, 132 KB

english, 2013

48

OP02.10: Slowing of fetal growth in late pregnancy is a feature of placental insufficiency among apparently well grown fetuses

Bardien, N., Whitehead, C., Tong, S., Walker, S. P.

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2013

Language:

english

File:

PDF, 56 KB

english, 2013

49

Double homozygous mutations (R275W and M432V) in the ParkinGene associated with late-onset Parkinson's disease

Carr, Jonathan, Guella, Ilaria, Szu-Tu, Chelsea, Boolay, Sihaam, Glanzmann, Brigitte, Farrer, Matthew J., Bardien, Soraya

Journal:

Movement Disorders

Year:

2016

Language:

english

File:

PDF, 1.06 MB

english, 2016

50

A new tool for prioritization of sequence variants from whole exome sequencing data

Glanzmann, Brigitte, Herbst, Hendri, Kinnear, Craig J., Möller, Marlo, Gamieldien, Junaid, Bardien, Soraya

Journal:

Source Code for Biology and Medicine

Year:

2016

Language:

english

File:

PDF, 523 KB

english, 2016

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