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Tazeen Ashraf | Researchclopedia

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Tazeen Ashraf

University of Technology Sydney ORCID

29

Works

476

Citations

9

h-index

9

i10-index

Research Topics

Genomics and Rare Diseases Genetics and Neurodevelopmental Disorders Genomic variations and chromosomal abnormalities

Affiliations

University of Technology Sydney2025–2025

Guy's Hospital2015–2016

Guy's and St Thomas' NHS Foundation Trust2007–2025

Great Ormond Street Hospital2023–2024

Great Ormond Street Hospital for Children NHS Foundation Trust2012–2025

Top Works

Clinical and genetic aspects of KBG syndrome

Karen Low,Tazeen Ashraf,et al.

2016137 citations

Epigenetics and DNA Methylation

Cannabis and Cannabinoid Research

Medical and legal confusion surrounding gamma-hydroxybutyrate (GHB) and its precursors gamma-butyrolactone (GBL) and 1,4-butanediol (1,4BD)

David M. Wood,Charlotte Warren‐Gash,et al.

200767 citations

Delineation of dominant and recessive forms of <i>LZTR1</i>‐associated Noonan syndrome

Alistair T. Pagnamenta,Pamela J. Kaisaki,et al.

201962 citations

The phenotype of Sotos syndrome in adulthood: A review of 44 individuals

Alison Foster,Anna Zachariou,et al.

201957 citations

Two further patients with the 1q24 deletion syndrome expand the phenotype: A possible role for the miR199–214 cluster in the skeletal features of the condition

Tazeen Ashraf,Morag N. Collinson,et al.

201537 citations

Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

Elke de Boer,Charlotte W. Ockeloen,et al.

202229 citations

Rothmund–Thomson Syndrome: novel pathogenic mutations and frequencies of variants in the <i><scp>RECQL</scp>4</i> and <i><scp>USB</scp>1 (C16orf57)</i> gene

Aude‐Annick Suter,Peter Itin,et al.

201619 citations

What evidence is there that the UK should tackle the potential emerging threat of methamphetamine toxicity rather than established recreational drugs such as MDMA ('ecstasy')?

David M. Wood,Jenny Button,et al.

200816 citations

<i>PUF60</i>‐related developmental disorder: A case series and phenotypic analysis of 10 additional patients with monoallelic <i>PUF60</i> variants

Hannah Grimes,Marc Ansari,et al.

202314 citations