RI Richards
RI Richards
Professor of Genetics, The University of Adelaide
Verified email at adelaide.edu.au
Cited by
Cited by
Guidelines for the use and interpretation of assays for monitoring autophagy
DJ Klionsky, K Abdelmohsen, A Abe, MJ Abedin, H Abeliovich, ...
Autophagy 12 (1), 1-222, 2016
Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever
I Aksentijevich, M Centola, ZM Deng, R Sood, JE Balow, G Wood, N Zaks, ...
Cell 90 (4), 797-807, 1997
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p (CCG) n
EJ Kremer, M Pritchard, M Lynch, S Yu, K Holman, E Baker, ST Warren, ...
Science 252 (5013), 1711, 1991
Characterization of DNA sequences through which cadmium and glucocorticoid hormones induce human metallothionein-IIA gene
M Karin, A Haslinger, H Holtgreve, RI Richards, P Krauter, HM Westphal, ...
Nature 308 (5959), 513-519, 1984
Fragile X genotype characterized by an unstable region of DNA.
S Yu, M Pritchard, E Kremer, M Lynch, J Nancarrow, E Baker, K Holman, ...
Science (New York, NY) 252 (5010), 1179, 1991
Incidence and origin of" null" alleles in the (AC) n microsatellite markers.
DF Callen, AD Thompson, Y Shen, HA Phillips, RI Richards, JC Mulley, ...
American journal of human genetics 52 (5), 922, 1993
Human metallothionein genes—primary structure of the metallothionein-II gene and a related processed gene
M Karin, RI Richards
Nature 299 (5886), 797-802, 1982
Simple tandem DNA repeats and human genetic disease
GR Sutherland, RI Richards
Proceedings of the National Academy of Sciences 92 (9), 3636, 1995
Dynamic mutations: a new class of mutations causing human disease.
RI Richards, GR Sutherland
Cell 70 (5), 709, 1992
Simple repeat DNA is not replicated simply
RI Richards, GR Sutherland
Nature Genetics 6 (2), 114-116, 1994
Structural and functional analysis of the human metallothionein-IA gene: differential induction by metal ions and glucocorticoids
RI Richards, A Heguy, M Karin
Cell 37 (1), 263-272, 1984
Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells
K Ried, M Finnis, L Hobson, M Mangelsdorf, S Dayan, JK Nancarrow, ...
Human molecular genetics 9 (11), 1651, 2000
Primary structure and evolution of rat growth hormone gene
A Barta, RI Richards, JD Baxter, J Shine
Proceedings of the National Academy of Sciences 78 (8), 4867, 1981
Structure of mouse kallikrein gene family suggests a role in specific processing of biologically active peptides
AJ Mason, BA Evans, DR Cox, J Shine, RI Richards
Nature 303 (5915), 300-307, 1983
Fragile and unstable chromosomes in cancer: causes and consequences
RI Richards
TRENDS in Genetics 17 (6), 339-345, 2001
Fragile-X syndrome: unique genetics of the heritable unstable element
S Yu, J Mulley, D Loesch, G Turner, A Donnelly, A Gedeon, D Hillen, ...
American journal of human genetics 50 (5), 968, 1992
A third Wilms' tumor locus on chromosome 16q
MA Maw, PE Grundy, LJ Millow, MR Eccles, RS Dunn, PJ Smith, ...
Cancer research 52 (11), 3094, 1992
Human metallothionein genes: structure of the functional locus at 16q13
AK West, R Stallings, CE Hildebrand, R Chiu, M Karin, RI Richards
Genomics 8 (3), 513-518, 1990
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease
D Ravine, SM Forrest, LJ Sheffield, DM Danks, RG Walker, ...
The Lancet 340 (8831), 1330-1333, 1992
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2
C Jones, L Penny, T Mattina, S Yu, E Baker, L Voullaire, WY Langdon, ...
Nature 376 (6536), 145-149, 1995
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