Micky Ovcaric

Variation in The Vitamin D Receptor Gene is Associated With Multiple Sclerosis in an Australian Population (2008)

Lotti Tajouri, Micky Ovcaric, Rob Curtain, Matthew P. Johnson, R. Griffiths, Peter Csurhes, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Linkage disequilibrium analysis in the genetically isolated Norfolk Island population (2008)

Bellis, Claire, Cox, Hannah, Ovcaric, Micky, Begley, Kimberly Nina, Lea, Rodney Arthur, Quinlan, Sharon Anne, ...

Norfolk Island is a human genetic isolate, possessing unique population characteristics that could be utilized for complex disease gene localization. Our intention was to evaluate the extent and...

Investigation of the NOTCH3 and TNFSF7 Genes on C19p13 as Candidates for Migraine (2008)

Smith, Robert Anthony, Curtain, Rob, Ovcaric, Micky, Tajouri, Lotfi, MacMillan, John, Griffiths, Lyn

To investigate the migraine locus around the C19p13 region through analysis of the NOTCH3 gene (C19p13.2- p13.1), previously shown to be a gene involved in CADASIL and the TNFSF7 gene (C19p13),...

Linkage disequilibrium analysis in the genetically isolated Norfolk Island population (2008)

Bellis, Claire, Cox, Hannah, Ovcaric, Micky, Begley, Kimberly Nina, Lea, Rodney Arthur, Quinlan, Sharon Anne, ...

Norfolk Island is a human genetic isolate, possessing unique population characteristics that could be utilized for complex disease gene localization. Our intention was to evaluate the extent and...

Investigation of the NOTCH3 and TNFSF7 Genes on C19p13 as Candidates for Migraine (2008)

Smith, Robert Anthony, Curtain, Rob, Ovcaric, Micky, Tajouri, Lotfi, MacMillan, John, Griffiths, Lyn

To investigate the migraine locus around the C19p13 region through analysis of the NOTCH3 gene (C19p13.2- p13.1), previously shown to be a gene involved in CADASIL and the TNFSF7 gene (C19p13),...

Linkage disequilibrium analysis in the genetically isolated Norfolk Island population (2008)

Bellis, Claire, Cox, Hannah, Ovcaric, Micky, Begley, Kimberly Nina, Lea, Rodney Arthur, Quinlan, Sharon Anne, ...

Norfolk Island is a human genetic isolate, possessing unique population characteristics that could be utilized for complex disease gene localization. Our intention was to evaluate the extent and...

Investigation of the NOTCH3 and TNFSF7 Genes on C19p13 as Candidates for Migraine (2008)

Smith, Robert Anthony, Curtain, Rob, Ovcaric, Micky, Tajouri, Lotfi, MacMillan, John, Griffiths, Lyn

To investigate the migraine locus around the C19p13 region through analysis of the NOTCH3 gene (C19p13.2- p13.1), previously shown to be a gene involved in CADASIL and the TNFSF7 gene (C19p13),...

Association analysis of chromosome 1 migraine candidate genes (2007)

Fernandez, Francesca, Curtain, Robert P, Colson, Natalie J, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn R

Abstract Background Migraine with aura (MA) is a subtype of typical migraine. Migraine with aura (MA) also encompasses a rare severe subtype Familial Hemiplegic Migraine (FHM) with several known...

Association analysis of chromosome 1 migraine candidate genes (2007)

Fernandez, Francesca, Curtain, Rob, Colson, Natalie Jane, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine with aura (MA) is a subtype of typical migraine. Migraine with aura (MA) also encompasses a rare severe subtype Familial Hemiplegic Migraine (FHM) with several known genetic loci....

Association analysis of chromosome 1 migraine candidate genes (2007)

Fernandez, Francesca, Curtain, Rob, Colson, Natalie Jane, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine with aura (MA) is a subtype of typical migraine. Migraine with aura (MA) also encompasses a rare severe subtype Familial Hemiplegic Migraine (FHM) with several known genetic loci....

Association analysis of chromosome 1 migraine candidate genes (2007)

Fernandez, Francesca, Curtain, Rob, Colson, Natalie Jane, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine with aura (MA) is a subtype of typical migraine. Migraine with aura (MA) also encompasses a rare severe subtype Familial Hemiplegic Migraine (FHM) with several known genetic loci....

Genetic Investigation of Methylenetetrahydrofolate Reductase (MTHFR) and Catechol-O-Methyl Transferase (COMT) in Multiple Sclerosis (2006)

Tajouri, Lotti, Martin, Virginie, Gasparini, Claudia, Ovcaric, Micky, Curtain, Rob, Lea, Rod A., ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

Genetic Investigation of Methylenetetrahydrofolate Reductase (MTHFR) and Catechol-O-Methyl Transferase (COMT) in Multiple Sclerosis (2006)

Tajouri, Lotti, Martin, Virginie, Gasparini, Claudia, Ovcaric, Micky, Curtain, Rob, Lea, Rod A., ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

Minor Head Trauma Induced Sporadic Hemiplegic Migraine (SHM) Coma (2006)

Curtain, Rob, Smith, Robert Anthony, Ovcaric, Micky, Griffiths, Lyn

Familial hemiplegic migraine is a severe, rare subtype of migraine. Gene mutations on chromosome 19 have been identified in the calcium channel, voltage-dependent, P/Q type, alpha-1A subunit gene...

Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol-O-methyl transferase (COMT) in multiple sclerosis (2006)

Tajouri, Lotfi, Martin, Virginie, Gasparini, Claudia Francesca, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

Minor Head Trauma Induced Sporadic Hemiplegic Migraine (SHM) Coma (2006)

Curtain, Rob, Smith, Robert Anthony, Ovcaric, Micky, Griffiths, Lyn

Yes

Genetic investigation of methylenetetrahydroxyfolate reductase (MTHFR) and catechol-o-methyl transferase (COMT) in multiple sclerosis. (2006)

Tajouri, Lotfi, Martin, Virginie, Gasparini, Claudia Francesca, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, ...

Yes

Association of the Vitamin D Receptor Gene with Multiple Sclerosis (2006)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Johnson, Matthew Peter, Csurhes, P., ...

No

Association of the Vitamin D Receptor Gene with Multiple Sclerosis (2006)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Johnson, Matthew Peter, Csurhes, P., ...

No

Minor Head Trauma Induced Sporadic Hemiplegic Migraine (SHM) Coma (2006)

Curtain, Rob, Smith, Robert Anthony, Ovcaric, Micky, Griffiths, Lyn

Familial hemiplegic migraine is a severe, rare subtype of migraine. Gene mutations on chromosome 19 have been identified in the calcium channel, voltage-dependent, P/Q type, alpha-1A subunit gene...

Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol-O-methyl transferase (COMT) in multiple sclerosis (2006)

Tajouri, Lotfi, Martin, Virginie, Gasparini, Claudia Francesca, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

Association of the Vitamin D Receptor Gene with Multiple Sclerosis (2006)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Johnson, Matthew Peter, Csurhes, P., ...

Genetic Investigation of Methylenetetrahydrofolate Reductase (MTHFR) and Catechol-O-Methyl Transferase (COMT) in Multiple Sclerosis (2006)

Tajouri, Lotti, Martin, Virginie, Gasparini, Claudia, Ovcaric, Micky, Curtain, Rob, Lea, Rod A., ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

Genetic Investigation of Methylenetetrahydrofolate Reductase (MTHFR) and Catechol-O-Methyl Transferase (COMT) in Multiple Sclerosis (2006)

Tajouri, Lotti, Martin, Virginie, Gasparini, Claudia, Ovcaric, Micky, Curtain, Rob, Lea, Rod A., ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

Minor Head Trauma Induced Sporadic Hemiplegic Migraine (SHM) Coma (2006)

Curtain, Rob, Smith, Robert Anthony, Ovcaric, Micky, Griffiths, Lyn

Familial hemiplegic migraine is a severe, rare subtype of migraine. Gene mutations on chromosome 19 have been identified in the calcium channel, voltage-dependent, P/Q type, alpha-1A subunit gene...

Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol-O-methyl transferase (COMT) in multiple sclerosis (2006)

Tajouri, Lotfi, Martin, Virginie, Gasparini, Claudia Francesca, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, ...

Multiple sclerosis (MS) is a chronic neurological disease characterized by central nervous system (CNS) inflammation and demyelination. The C677T substitution variant in the methylenetetrahydrofolate...

Association of the Vitamin D Receptor Gene with Multiple Sclerosis (2006)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Johnson, Matthew Peter, Csurhes, P., ...

Variation in The Vitamin D Receptor Gene is Associated With Multiple Sclerosis in an Australian Population (2005)

Tajouri, Lotti, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew P., Griffiths, Lyn R., Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Variation in The Vitamin D Receptor Gene is Associated With Multiple Sclerosis in an Australian Population (2005)

Tajouri, Lotti, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew P., Griffiths, Lyn R., Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Variation in The Vitamin D Receptor Gene is Associated With Multiple Sclerosis in an Australian Population (2005)

Tajouri, Lotti, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew P., Griffiths, Lyn R., Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility. (2005)

Curtain, Rob, Sundholm, James Rodney, Lea, Rodney Arthur, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn, ...

Page numbers are not for citation purposes. Instead, this article has the unique article number of 32.

Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees (2005)

Curtain, Rob, Lea, Rodney Arthur, Tajouri, Lotfi, Haupt, Larisa, Ovcaric, Micky, MacMillan, J., ...

Yes

Genetic variants of angiotensin converting enzyme and methylenetetrahydrofolate reductase may act in combination to increase migraine susceptibility. (2005)

Lea, Rodney Arthur, Ovcaric, Micky, Sundholm, James Rodney, Solyom, Leah, MacMillian, John, Griffiths, Lyn, ...

Yes

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine. (2005)

Lea, Rodney Arthur, Nyholt, D. R., Curtain, Rob, Ovcaric, Micky, Sciascia, Rachel, Bellis, Claire, ...

Yes

Variation in the vitamin D receptor gene is associated with multiple sclerosis in an Australian population. (2005)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew Peter, Griffiths, Lyn, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility. (2005)

Curtain, Rob, Sundholm, James Rodney, Lea, Rodney Arthur, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine is a polygenic multifactorial disease, possessing environmental and genetic causative factors with multiple involved genes. Mutations in various ion channel genes are responsible...

Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees (2005)

Curtain, Rob, Lea, Rodney Arthur, Tajouri, Lotfi, Haupt, Larisa, Ovcaric, Micky, MacMillan, J., ...

Yes

Genetic variants of angiotensin converting enzyme and methylenetetrahydrofolate reductase may act in combination to increase migraine susceptibility. (2005)

Lea, Rodney Arthur, Ovcaric, Micky, Sundholm, James Rodney, Solyom, Leah, MacMillian, John, Griffiths, Lyn

Migraine, with and without aura (MA and MO), is a prevalent and complex neurovascular disorder that is likely to be influenced by multiple genes some of which may be capable of causing vascular...

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine. (2005)

Lea, Rodney Arthur, Nyholt, D. R., Curtain, Rob, Ovcaric, Micky, Sciascia, Rachel, Bellis, Claire, ...

Migraine is a prevalent neurovascular disease with a significant genetic component. Linkage studies have so far identified migraine susceptibility loci on chromosomes 1, 4, 6, 11, 14, 19 and X. We...

Variation in the vitamin D receptor gene is associated with multiple sclerosis in an Australian population. (2005)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew Peter, Griffiths, Lyn, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility. (2005)

Curtain, Rob, Sundholm, James Rodney, Lea, Rodney Arthur, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine is a polygenic multifactorial disease, possessing environmental and genetic causative factors with multiple involved genes. Mutations in various ion channel genes are responsible...

Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees (2005)

Curtain, Rob, Lea, Rodney Arthur, Tajouri, Lotfi, Haupt, Larisa, Ovcaric, Micky, MacMillan, J., ...

Genetic variants of angiotensin converting enzyme and methylenetetrahydrofolate reductase may act in combination to increase migraine susceptibility. (2005)

Lea, Rodney Arthur, Ovcaric, Micky, Sundholm, James Rodney, Solyom, Leah, MacMillian, John, Griffiths, Lyn

Migraine, with and without aura (MA and MO), is a prevalent and complex neurovascular disorder that is likely to be influenced by multiple genes some of which may be capable of causing vascular...

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine. (2005)

Lea, Rodney Arthur, Nyholt, D. R., Curtain, Rob, Ovcaric, Micky, Sciascia, Rachel, Bellis, Claire, ...

Migraine is a prevalent neurovascular disease with a significant genetic component. Linkage studies have so far identified migraine susceptibility loci on chromosomes 1, 4, 6, 11, 14, 19 and X. We...

Variation in the vitamin D receptor gene is associated with multiple sclerosis in an Australian population. (2005)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew Peter, Griffiths, Lyn, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Variation in The Vitamin D Receptor Gene is Associated With Multiple Sclerosis in an Australian Population (2005)

Tajouri, Lotti, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew P., Griffiths, Lyn R., Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Variation in The Vitamin D Receptor Gene is Associated With Multiple Sclerosis in an Australian Population (2005)

Tajouri, Lotti, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew P., Griffiths, Lyn R., Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility. (2005)

Curtain, Rob, Sundholm, James Rodney, Lea, Rodney Arthur, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn

Background Migraine is a polygenic multifactorial disease, possessing environmental and genetic causative factors with multiple involved genes. Mutations in various ion channel genes are responsible...

Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees (2005)

Curtain, Rob, Lea, Rodney Arthur, Tajouri, Lotfi, Haupt, Larisa, Ovcaric, Micky, MacMillan, J., ...

Genetic variants of angiotensin converting enzyme and methylenetetrahydrofolate reductase may act in combination to increase migraine susceptibility. (2005)

Lea, Rodney Arthur, Ovcaric, Micky, Sundholm, James Rodney, Solyom, Leah, MacMillian, John, Griffiths, Lyn

Migraine, with and without aura (MA and MO), is a prevalent and complex neurovascular disorder that is likely to be influenced by multiple genes some of which may be capable of causing vascular...

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine. (2005)

Lea, Rodney Arthur, Nyholt, D. R., Curtain, Rob, Ovcaric, Micky, Sciascia, Rachel, Bellis, Claire, ...

Migraine is a prevalent neurovascular disease with a significant genetic component. Linkage studies have so far identified migraine susceptibility loci on chromosomes 1, 4, 6, 11, 14, 19 and X. We...

Variation in the vitamin D receptor gene is associated with multiple sclerosis in an Australian population. (2005)

Tajouri, Lotfi, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew Peter, Griffiths, Lyn, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher...

Investigation Of An Inducible Nitric Oxide Synthase Gene (NOS2A) Polymorphism In A Multiple Sclerosis Population (2004)

Tajouri, Lotti, Martin, Virginie, Ovcaric, Micky, Curtain, Rob P., Lea, Rod A., Csurhes, Peter, ...

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide (NO) is a biological signaling and...

Investigation Of An Inducible Nitric Oxide Synthase Gene (NOS2A) Polymorphism In A Multiple Sclerosis Population (2004)

Tajouri, Lotti, Martin, Virginie, Ovcaric, Micky, Curtain, Rob P., Lea, Rod A., Csurhes, Peter, ...

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide (NO) is a biological signaling and...

Investigation of a Neuronal Nitric Oxide Synthase Gene (NOS1) Polymorphism in a Multiple Sclerosis Population (2004)

Tajouri, Lotti, Ferreira, Linda, Ovcaric, Micky, Curtain, Rob, Lea, Rod, Csurhes, Peter A., ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Investigation of a Neuronal Nitric Oxide Synthase Gene (NOS1) Polymorphism in a Multiple Sclerosis Population (2004)

Tajouri, Lotti, Ferreira, Linda, Ovcaric, Micky, Curtain, Rob, Lea, Rod, Csurhes, Peter A., ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura (2004)

Lea, Rod A, Ovcaric, Micky, Sundholm, James, MacMillan, John, Griffiths, Lyn R

Abstract Background The C677T variant in the methylenetetrahydrofolate reductase (MTHFR) gene is associated with increased levels of circulating homocysteine and is a mild risk factor for vascular...

The role of adenosine-related genes variants in susceptibility to essential hypertension (2004)

Wright, Kirsty, Tajouri, Lotfi, Lea, Rodney Arthur, Ovcaric, Micky, Heuy, Stephanie, Morin, Fabien, ...

Yes

The Methylentetrahydrofolate Reductase Gene Variant (C677T) as a Risk Factor for Essential Hypertension in Caucasions (2004)

Heuy, Stephanie, MORIN, Fabien, Lea, Rodney Arthur, Ovcaric, Micky, Tajouri, Lotfi, Griffiths, Lyn

Yes

Investigation of an unducible nitric oxide synthase gene (NOS2A) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Martin, Virginie, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide (NO) is a biological signaling and...

The methylenetetrahydofolate reductase gene variant C677T influences susceptibility to migraine with aura (2004)

Lea, Rodney Arthur, Ovcaric, Micky, Sundholm, James, MacMillan, John, Griffiths, Lyn

Page numbers are not for citation purposes. Instead, this article has the unique article number of 3.

Investigation of a neuronal nitric oxide synthase gene (NOS1) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Ferreira, Linda Anne, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Norfolk Island Population Origin Analysis (2004)

Bellis, Claire, Ovcaric, Micky, Lea, Rodney Arthur, Heath, S., Blangero, J., Griffiths, Lyn, ...

No

The role of adenosine-related genes variants in susceptibility to essential hypertension (2004)

Wright, Kirsty, Tajouri, Lotfi, Lea, Rodney Arthur, Ovcaric, Micky, Heuy, Stephanie, Morin, Fabien, ...

Yes

The Methylentetrahydrofolate Reductase Gene Variant (C677T) as a Risk Factor for Essential Hypertension in Caucasions (2004)

Heuy, Stephanie, Morin, Fabien, Lea, Rodney Arthur, Ovcaric, Micky, Tajouri, Lotfi, Griffiths, Lyn

Essential hypertension (EH) is a common, multifactorial disorder likely to be influenced by multiple genes of modest effect. The methylenetetrahydrofolate reductase (MTHFR) gene C677T mutation is...

Investigation of an unducible nitric oxide synthase gene (NOS2A) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Martin, Virginie, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide (NO) is a biological signaling and...

The methylenetetrahydofolate reductase gene variant C677T influences susceptibility to migraine with aura (2004)

Lea, Rodney Arthur, Ovcaric, Micky, Sundholm, James, MacMillan, John, Griffiths, Lyn

Background The C677T variant in the methylenetetrahydrofolate reductase (MTHFR) gene is associated with increased levels of circulating homocysteine and is a mild risk factor for vascular disease....

Investigation of a neuronal nitric oxide synthase gene (NOS1) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Ferreira, Linda Anne, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Norfolk Island Population Origin Analysis (2004)

Bellis, Claire, Ovcaric, Micky, Lea, Rodney Arthur, Heath, S., Blangero, J., Griffiths, Lyn

No

The role of adenosine-related genes variants in susceptibility to essential hypertension (2004)

Wright, Kirsty, Tajouri, Lotfi, Lea, Rodney Arthur, Ovcaric, Micky, Heuy, Stephanie, Morin, Fabien, ...

The Methylentetrahydrofolate Reductase Gene Variant (C677T) as a Risk Factor for Essential Hypertension in Caucasions (2004)

Heuy, Stephanie, Morin, Fabien, Lea, Rodney Arthur, Ovcaric, Micky, Tajouri, Lotfi, Griffiths, Lyn

Essential hypertension (EH) is a common, multifactorial disorder likely to be influenced by multiple genes of modest effect. The methylenetetrahydrofolate reductase (MTHFR) gene C677T mutation is...

Investigation of an unducible nitric oxide synthase gene (NOS2A) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Martin, Virginie, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide (NO) is a biological signaling and...

The methylenetetrahydofolate reductase gene variant C677T influences susceptibility to migraine with aura (2004)

Lea, Rodney Arthur, Ovcaric, Micky, Sundholm, James, MacMillan, John, Griffiths, Lyn

Background The C677T variant in the methylenetetrahydrofolate reductase (MTHFR) gene is associated with increased levels of circulating homocysteine and is a mild risk factor for vascular disease....

Investigation of a neuronal nitric oxide synthase gene (NOS1) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Ferreira, Linda Anne, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Norfolk Island Population Origin Analysis (2004)

Bellis, Claire, Ovcaric, Micky, Lea, Rodney Arthur, Heath, S., Blangero, J., Griffiths, Lyn

Investigation of a Neuronal Nitric Oxide Synthase Gene (NOS1) Polymorphism in a Multiple Sclerosis Population (2004)

Tajouri, Lotti, Ferreira, Linda, Ovcaric, Micky, Curtain, Rob, Lea, Rod, Csurhes, Peter A., ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Investigation Of An Inducible Nitric Oxide Synthase Gene (NOS2A) Polymorphism In A Multiple Sclerosis Population (2004)

Tajouri, Lotti, Martin, Virginie, Ovcaric, Micky, Curtain, Rob P., Lea, Rod A., Csurhes, Peter, ...

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide (NO) is a biological signaling and...

Investigation of a Neuronal Nitric Oxide Synthase Gene (NOS1) Polymorphism in a Multiple Sclerosis Population (2004)

Tajouri, Lotti, Ferreira, Linda, Ovcaric, Micky, Curtain, Rob, Lea, Rod, Csurhes, Peter A., ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Investigation Of An Inducible Nitric Oxide Synthase Gene (NOS2A) Polymorphism In A Multiple Sclerosis Population (2004)

Tajouri, Lotti, Martin, Virginie, Ovcaric, Micky, Curtain, Rob P., Lea, Rod A., Csurhes, Peter, ...

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide (NO) is a biological signaling and...

The role of adenosine-related genes variants in susceptibility to essential hypertension (2004)

Wright, Kirsty, Tajouri, Lotfi, Lea, Rodney Arthur, Ovcaric, Micky, Heuy, Stephanie, Morin, Fabien, ...

The Methylentetrahydrofolate Reductase Gene Variant (C677T) as a Risk Factor for Essential Hypertension in Caucasions (2004)

Heuy, Stephanie, Morin, Fabien, Lea, Rodney Arthur, Ovcaric, Micky, Tajouri, Lotfi, Griffiths, Lyn

Essential hypertension (EH) is a common, multifactorial disorder likely to be influenced by multiple genes of modest effect. The methylenetetrahydrofolate reductase (MTHFR) gene C677T mutation is...

Investigation of an unducible nitric oxide synthase gene (NOS2A) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Martin, Virginie, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) affecting most commonly the Caucasian population. Nitric oxide (NO) is a biological signaling and...

The methylenetetrahydofolate reductase gene variant C677T influences susceptibility to migraine with aura (2004)

Lea, Rodney Arthur, Ovcaric, Micky, Sundholm, James, MacMillan, John, Griffiths, Lyn

Background The C677T variant in the methylenetetrahydrofolate reductase (MTHFR) gene is associated with increased levels of circulating homocysteine and is a mild risk factor for vascular disease....

Investigation of a neuronal nitric oxide synthase gene (NOS1) polymorphism in a multiple sclerosis population (2004)

Tajouri, Lotfi, Ferreira, Linda Anne, Ovcaric, Micky, Curtain, Rob, Lea, Rodney Arthur, Csurhes, Peter, ...

Multiple Sclerosis (MS) is a chronic neurological disease characterized by demyelination associated with infiltrating white blood cells in the central nervous system (CNS). Nitric oxide synthases...

Norfolk Island Population Origin Analysis (2004)

Bellis, Claire, Ovcaric, Micky, Lea, Rodney Arthur, Heath, S., Blangero, J., Griffiths, Lyn

The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura

Lea, Rod A, Ovcaric, Micky, Sundholm, James, MacMillan, John, Griffiths, Lyn R

The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura

Lea, Rod A, Ovcaric, Micky, Sundholm, James, MacMillan, John, Griffiths, Lyn R

Association analysis of chromosome 1 migraine candidate genes

Fernandez, Francesca, Curtain, Robert P, Colson, Natalie J, Ovcaric, Micky, MacMillan, John, Griffiths, Lyn R