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Employment (1)

Health Support Queensland Pathology Queensland: Herston, QLD, AU

1995 to 2018-06-29 | Supervising Scientist (Molecular Genetics Laboratory)
Employment
Source: Self-asserted source
Valentine Hyland

Education and qualifications (1)

Royal College of Pathologists of Australasia: Surry Hills, NSW, AU

2011 to 2011 | Fellow Faculty of Science (Molecular Genetics)
Education
Source: Self-asserted source
Valentine Hyland

Works (50 of 67)

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Demonstration of a novel Xp22.2 microdeletion as the cause of familial extreme skewing of X-inactivation utilizing case-parent trio SNP microarray analysis.

Molecular genetics & genomic medicine
2018-05 | Journal article
DOI: 10.1002/mgg3.378
PMID: 29490426
Contributors: Mason JA; Aung HT; Nandini A; Woods RG; Fairbairn DJ; Rowell JA; Young D; Susman RD; Brown SA; Hyland VJ et al.
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Digenic inheritance in epidermolysis bullosa simplex involving two novel mutations in KRT5 and KRT14.

The British journal of dermatology
2017-07 | Journal article
DOI: 10.1111/bjd.15053
PMID: 27611893
Contributors: Kim E; Harris A; Hyland V; Murrell DF
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

A protocol for the identification and validation of novel genetic causes of kidney disease.

BMC nephrology
2015 | Journal article
DOI: 10.1186/s12882-015-0148-8
PMID: 26374634
PMC: PMC4570515
Contributors: Mallett A; Patel C; Maier B; McGaughran J; Gabbett M; Takasato M; Cameron A; Trnka P; Alexander SI; Rangan G et al.
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Atypical HUS associated with severe, unexpected antibody-mediated rejection post kidney transplant.

Nephrology (Carlton, Vic.)
2014-04 | Journal article
DOI: 10.1111/nep.12195
PMID: 24460647
Contributors: Stevenson S; Mallett A; Oliver K; Hyland V; Hawley C; Malmanche T; Isbel N
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project.

Genetics in medicine : official journal of the American College of Medical Genetics
2009-12 | Journal article
DOI: 10.1097/gim.0b013e3181c371c5
PMID: 20010362
Contributors: Cotton RG; Al Aqeel AI; Al-Mulla F; Carrera P; Claustres M; Ekong R; Hyland VJ; Macrae FA; Marafie MJ; Paalman MH et al.
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Proceedings of the Australasian Association of Clinical Biochemists’ 47th Annual Scientific Conference.

The Clinical biochemist. Reviews
2009-11 | Journal article
PMC: PMC2791774
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

DNA elution from buccal cells stored on Whatman FTA Classic Cards using a modified methanol fixation method.

BioTechniques
2009-04 | Journal article
DOI: 10.2144/000113077
PMID: 19450238
Contributors: Johanson HC; Hyland V; Wicking C; Sturm RA
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.

Proceedings of the National Academy of Sciences of the United States of America
2004-05 | Journal article
DOI: 10.1073/pnas.0308475101
PMID: 15141091
PMC: PMC419562
Contributors: Ruf RG; Xu PX; Silvius D; Otto EA; Beekmann F; Muerb UT; Kumar S; Neuhaus TJ; Kemper MJ; Raymond RM et al.
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Effect of 24 months of recombinant growth hormone on height and body proportions in SHOX haploinsufficiency.

Journal of pediatric endocrinology & metabolism : JPEM
2003-09 | Journal article
DOI: 10.1515/jpem.2003.16.7.997
PMID: 14513876
Contributors: Munns CF; Berry M; Vickers D; Rappold GA; Hyland VJ; Glass IA; Batch JA
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Familial growth and skeletal features associated with SHOX haploinsufficiency.

Journal of pediatric endocrinology & metabolism : JPEM
2003-09 | Journal article
DOI: 10.1515/jpem.2003.16.7.987
PMID: 14513875
Contributors: Munns CF; Glass IA; Flanagan S; Hayes M; Williams B; Berry M; Vickers D; O'Rourke P; Rao E; Rappold GA et al.
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3.

Journal of medical genetics
2003-07 | Journal article
DOI: 10.1136/jmg.40.7.515
PMID: 12843324
PMC: PMC1735534
Contributors: Ruf RG; Berkman J; Wolf MT; Nurnberg P; Gattas M; Ruf EM; Hyland V; Kromberg J; Glass I; Macmillan J et al.
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Somatic and germline mosaicism for a R248C missense mutation in FGFR3, resulting in a skeletal dysplasia distinct from thanatophoric dysplasia.

American journal of medical genetics. Part A
2003-07 | Journal article
DOI: 10.1002/ajmg.a.20012
PMID: 12833394
Contributors: Hyland VJ; Robertson SP; Flanagan S; Savarirayan R; Roscioli T; Masel J; Hayes M; Glass IA
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhood.

Journal of medical genetics
2002-10 | Journal article
DOI: 10.1136/jmg.39.10.758
PMID: 12362035
PMC: PMC1734979
Contributors: Flanagan SF; Munns CF; Hayes M; Williams B; Berry M; Vickers D; Rao E; Rappold GA; Batch JA; Hyland VJ et al.
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy): an Australian perspective.

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
2001-09 | Journal article
DOI: 10.1054/jocn.2000.0848
PMID: 11535004
Contributors: Chuah TL; Tan KM; Flanagan S; Hyland V; Sullivan AA; Henderson R; MacMillan J; Lander C
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Solid-phase amplification for detection of C282y and H63D hemochromatosis (HFE) gene mutations.

Clinical chemistry
2001-08 | Journal article
PMID: 11468226
Contributors: Turner MS; Penning S; Sharp A; Hyland VJ; Harris R; Morris CP; van Daal A
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Histopathological analysis of Leri-Weill dyschondrosteosis: disordered growth plate.

Hand surgery : an international journal devoted to hand and upper limb surgery and related research : journal of the Asia-Pacific Federation of Societies for Surgery of the Hand
2001-07 | Journal article
DOI: 10.1142/s0218810401000424
PMID: 11677662
Contributors: Munns CF; Glass IA; LaBrom R; Hayes M; Flanagan S; Berry M; Hyland VJ; Batch JA; Philips GE; Vickers D
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Premature calvarial synostosis and epidermal hyperplasia (Beare-Stevenson syndrome-like anomalies) resulting from a P250R missense mutation in the gene encoding fibroblast growth factor receptor 3.

American journal of medical genetics
2001-07 | Journal article
DOI: 10.1002/ajmg.1369
PMID: 11424131
Contributors: Roscioli T; Flanagan S; Mortimore RJ; Kumar P; Weedon D; Masel J; Lewandowski R; Hyland V; Glass IA
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Height discordance in monozygotic females is not attributable to discordant inactivation of X-linked stature determining genes.

Twin research : the official journal of the International Society for Twin Studies
2001-02 | Journal article
DOI: 10.1375/1369052012100
PMID: 11665320
Contributors: Healey SC; Kirk KM; Hyland VJ; Munns CF; Henders AK; Batch JA; Heath AC; Martin NG; Glass IA
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Large hepatic mitochondrial DNA deletions associated with L-lactic acidosis and highly active antiretroviral therapy.

AIDS (London, England)
2001-02 | Journal article
DOI: 10.1097/00002030-200102160-00018
PMID: 11273225
Contributors: Bartley PB; Westacott L; Boots RJ; Lawson M; Potter JM; Hyland VJ; Woods ML
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Clinical findings in a patient with FGFR1 P252R mutation and comparison with the literature.

American journal of medical genetics
2000-07 | Journal article
DOI: 10.1002/1096-8628(20000703)93:1<22::aid-ajmg5>3.0.co;2-u
PMID: 10861678
Contributors: Roscioli T; Flanagan S; Kumar P; Masel J; Gattas M; Hyland VJ; Glass IA
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Glucocorticoids differentially inhibit expression of the RET proto-oncogene.

Gene expression
1999 | Journal article
PMID: 10947080
Contributors: Capes-Davis A; Andrew SD; Hyland VJ; Twigg S; Learoyd DL; Dwight T; Marsh DJ; Robinson BG
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Molecular detection of prostate cells in ejaculate and urethral washings in men with suspected prostate cancer.

The Journal of urology
1999-04 | Journal article
DOI: 10.1097/00005392-199904000-00092
PMID: 10081904
Contributors: Clements JA; Rohde P; Allen V; Hyland VJ; Samaratunga ML; Tilley WD; Lavin MF; Gardiner RA
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Absence of MEN2A- or 2B-type RET mutations in primary neuroblastoma tumour tissue.

Molecular and cellular probes
1998-08 | Journal article
DOI: 10.1006/mcpr.1998.0181
PMID: 9727201
Contributors: Peaston AE; Camacho ML; Norris MD; Haber M; Marsh DJ; Robinson BG; Hyland VJ; Marshall GM
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Re: Malignant cytological washings from radical prostatectomy specimens: a possible mechanism for local recurrence of prostate cancer following surgical treatment of organ confined disease.

The Journal of urology
1997-09 | Journal article
DOI: 10.1097/00005392-199709000-00066
PMID: 9258113
Contributors: Gardiner RA; Samaratunga ML; Rohde P; Clements JA; Hyland V; Lavin MF
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Family and twin studies in systemic lupus erythematosus.

Disease markers
1997-04 | Journal article
PMID: 9160184
Contributors: Grennan DM; Parfitt A; Manolios N; Huang Q; Hyland V; Dunckley H; Doran T; Gatenby P; Badcock C
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Regulation of adhesion molecule expression by human synovial microvascular endothelial cells in vitro.

Arthritis and rheumatism
1996-03 | Journal article
DOI: 10.1002/art.1780390315
PMID: 8607896
Contributors: To SS; Newman PM; Hyland VJ; Robinson BG; Schrieber L
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

The identification of false positive responses to the pentagastrin stimulation test in RET mutation negative members of MEN 2A families.

Clinical endocrinology
1996-02 | Journal article
DOI: 10.1046/j.1365-2265.1996.505292.x
PMID: 8849577
Contributors: Marsh DJ; McDowall D; Hyland VJ; Andrew SD; Schnitzler M; Gaskin EL; Nevell DF; Diamond T; Delbridge L; Clifton-Bligh P et al.
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Increased frequency of the uncommon allele of a tumour necrosis factor alpha gene polymorphism in rheumatoid arthritis and systemic lupus erythematosus.

Disease markers
1995-03 | Journal article
PMID: 7614782
Contributors: Danis VA; Millington M; Hyland V; Lawford R; Huang Q; Grennan D
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Lack of association between an interleukin-1 receptor antagonist gene polymorphism and systemic lupus erythematosus.

Disease markers
1995-03 | Journal article
PMID: 7614783
Contributors: Danis VA; Millington M; Huang Q; Hyland V; Grennan D
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Cytokine production by normal human monocytes: inter-subject variation and relationship to an IL-1 receptor antagonist (IL-1Ra) gene polymorphism.

Clinical and experimental immunology
1995-02 | Journal article
DOI: 10.1111/j.1365-2249.1995.tb05549.x
PMID: 7851026
Contributors: Danis VA; Millington M; Hyland VJ; Grennan D
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.

Human molecular genetics
1994-12 | Journal article
DOI: 10.1093/hmg/3.12.2163
PMID: 7881414
Contributors: Mulligan LM; Eng C; Attié T; Lyonnet S; Marsh DJ; Hyland VJ; Robinson BG; Frilling A; Verellen-Dumoulin C; Safar A
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Effect of gold sodium thiomalate and its thiomalate component on the in vitro expression of endothelial cell adhesion molecules.

The Journal of clinical investigation
1994-11 | Journal article
DOI: 10.1172/jci117536
PMID: 7525650
PMC: PMC294592
Contributors: Newman PM; To SS; Robinson BG; Hyland VJ; Schrieber L
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

A rapid screening method for the detection of mutations in the RET proto-oncogene in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma families.

Genomics
1994-09 | Journal article
DOI: 10.1006/geno.1994.1526
PMID: 7835899
Contributors: Marsh DJ; Robinson BG; Andrew S; Richardson AL; Pojer R; Schnitzler M; Mulligan LM; Hyland VJ
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Secretory leucocyte proteinase inhibitor is produced by human articular cartilage chondrocytes and intervertebral disc fibrochondrocytes.

European journal of biochemistry
1993-12 | Journal article
DOI: 10.1111/j.1432-1033.1993.tb18452.x
PMID: 7904240
Contributors: Jacoby AS; Melrose J; Robinson BG; Hyland VJ; Ghosh P
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Medullary thyroid carcinoma: Australian experience with genetic testing.

Henry Ford Hospital medical journal
1992 | Journal article
PMID: 1362409
Contributors: Ward JL; Hyland VJ; Andrew DS; Marsh DJ; Robinson BG
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Sperm microinjection twins: deoxyribonucleic acid fingerprinting.

Fertility and sterility
1992-06 | Journal article
PMID: 1601162
Contributors: Saunders DM; Porter RN; Krzyminska UB; O'Neill C; Ward JL; Robinson BG; Hyland VJ
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15.

Mammalian genome : official journal of the International Mammalian Genome Society
1991 | Journal article
DOI: 10.1007/bf00350846
PMID: 1724400
Contributors: MacKinnon PJ; Powell BC; Rogers GE; Baker EG; MacKinnon RN; Hyland VJ; Callen DF; Sutherland GR
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Dinucleotide repeat polymorphism at D16S287.

Nucleic Acids Research
1991-12 | Journal article
DOI: 10.1093/nar/19.23.6664
PMID: 1754417
PMC: PMC329272
Contributors: Phillips HA; Hyland VJ; Holman K; Callen DF; Richards RI; Mulley JC
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Isolation of a human DNA sequence which spans the fragile X.

American journal of human genetics
1991-09 | Journal article
PMID: 1882843
PMC: PMC1683130
Contributors: Kremer EJ; Yu S; Pritchard M; Nagaraja R; Heitz D; Lynch M; Baker E; Hyland VJ; Little RD; Wada M
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.

American Journal of Human Genetics
1991-06 | Journal article
PMID: 2035525
PMC: PMC1683096
Contributors: Richards RI; Shen Y; Holman K; Kozman H; Hyland VJ; Mulley JC; Sutherland GR
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Genetic mapping of new RFLPs at Xq27-q28.

Genomics
1991-01 | Journal article
DOI: 10.1016/0888-7543(91)90218-4
PMID: 1672291
Contributors: Suthers GK; Oberlé I; Nancarrow J; Mulley JC; Hyland VJ; Wilson PJ; McCure J; Morris CP; Hopwood JJ; Mandel JL
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines.

American journal of human genetics
1990-08 | Journal article
PMID: 2378346
PMC: PMC1683725
Contributors: Suthers GK; Hyland VJ; Callen DF; Oberle I; Rocchi M; Thomas NS; Morris CP; Schwartz CE; Schmidt M; Ropers HH
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1.

Human genetics
1990-02 | Journal article
DOI: 10.1007/bf00200577
PMID: 1968038
Contributors: Hyland VJ; Suthers GK; Friend K; MacKinnon RN; Callen DF; Breuning MH; Keith T; Brown VA; Phipps P; Sutherland GR
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

A new DNA marker tightly linked to the fragile X locus (FRAXA).

Science (New York, N.Y.)
1989-12 | Journal article
DOI: 10.1126/science.2573953
PMID: 2573953
Contributors: Suthers GK; Callen DF; Hyland VJ; Kozman HM; Baker E; Eyre H; Harper PS; Roberts SH; Hors-Cayla MC; Davies KE
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Deletion analysis for Duchenne (and Becker) muscular dystrophy.

Australian paediatric journal
1989-10 | Journal article
PMID: 2590130
Contributors: Kimber RD; Hyland VJ; Haan EA; Mulley JC
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

A TaqI RFLP detected by the probe VK45C6 [D16S131] at 16p13.11.

Nucleic acids research
1989-08 | Journal article
DOI: 10.1093/nar/17.15.6430
PMID: 2570409
PMC: PMC318329
Contributors: Hyland VJ; Friend K; Sutherland GR
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X.

Human genetics
1989-08 | Journal article
DOI: 10.1007/bf00274150
PMID: 2570019
Contributors: Hyland VJ; Fernandez KE; Callen DF; MacKinnon RN; Baker E; Friend K; Sutherland GR
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

A linkage group with FRA16B (the fragile site at 16q22.1).

Human genetics
1989-05 | Journal article
DOI: 10.1007/bf00284044
PMID: 2722188
Contributors: Mulley JC; Hyland VJ; Fratini A; Bates LJ; Gedeon AK; Sutherland GR
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

Mapping the short arm of human chromosome 16.

Genomics
1989-04 | Journal article
DOI: 10.1016/0888-7543(89)90341-8
PMID: 2714795
Contributors: Callen DF; Hyland VJ; Baker EG; Fratini A; Gedeon AK; Mulley JC; Fernandez KE; Breuning MH; Sutherland GR
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central

The gene for human leukemia inhibitory factor (LIF) maps to 22q12.

Leukemia
1989-01 | Journal article
PMID: 2491897
Contributors: Sutherland GR; Baker E; Hyland VJ; Callen DF; Stahl J; Gough NM
Source: Self-asserted source
Valentine Hyland via Europe PubMed Central
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