Author

Merran Finnis

Observed names: M Finnis, M. Finnis, Merran L Finnis, Merran L. Finnis

Institutions: South Australia Pathology, Women's and Children's Hospital

Observed institutions: South Australia Pathology, Women's and Children's Hospital, Women's and Children's Health Network, National Health and Medical Research Council, Adelaide University, The University of Adelaide

OpenAlex ID: A5000796692

Chromosomal fragile site FRA16D and DNA instability in cancer.

2000 · M Mangelsdorf, K Ried, et al. · PubMed · 115

Microfibril-associated Glycoprotein-2 (MAGP-2) Is Specifically Associated with Fibrillin-containing Microfibrils but Exhibits More Restricted Patterns of Tissue Localization and Developmental Expression Than Its Structural Relative MAGP-1

1998 · Mark A. Gibson, Merran L. Finnis, et al. · Journal of Histochemistry & Cytochemistry · 99

Microfibril-associated Glycoprotein-1 (MAGP-1) Binds to the Pepsin-resistant Domain of the α3(VI) Chain of Type VI Collagen

1997 · Merran L Finnis, Mark A Gibson · Journal of Biological Chemistry · 96

Common chromosomal fragile site FRA16D mutation in cancer cells

2005 · Merran Finnis, Sonia Dayan, et al. · Human Molecular Genetics · 83

Aristaless-related homeobox gene, the gene responsible for West syndrome and related disorders, is a Groucho/transducin-like enhancer of split dependent transcriptional repressor

2007 · O. McKenzie, I. Ponte, et al. · Neuroscience · 75

Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein

2004 · Theologia Sarafidou, Christina Kahl, et al. · Genomics · 71

Ohtahara syndrome in a family with an ARX protein truncation mutation (c.81C>G/p.Y27X)

2009 · Tod Fullston, Louise Brueton, et al. · European Journal of Human Genetics · 38

XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene

2005 · Monica L Stepp, A Lauren Cason, et al. · BMC Medical Genetics · 35

Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene

2011 · T Fullston, M Finnis, et al. · Clinical Genetics · 28

Developmental expression of dermatan sulfate proteoglycans in the elastic bovine nuchal ligament

2000 · Betty J Reinboth, Merran L Finnis, et al. · Matrix Biology · 22

AFX mutations frequently cause X-linked mental retardation

2002 · Marie Mangelsdorf, Merran Finnis, et al. · The American Journal of Human Genetics

Works count: 13

Citation count: 662

H-index: 10

I10-index: 10