World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
52
Citations
10745
World Ranking
16612
National Ranking
466

Overview

Carol Wicking is affiliated with the University of Queensland in Australia. Their research spans multiple fields including Biochemistry, Genetics and Molecular Biology, Medicine, and Immunology and Microbiology.

Their work delves into specialized subfields such as Genetics, Pulmonary and Respiratory Medicine, and Immunology. These areas underpin the main themes of their research, which focus on Genomics and Rare Diseases, Cystic Fibrosis Research Advances, and Immunodeficiency and Autoimmune Disorders.

Carol Wicking has contributed to academic literature with publications including the paper titled "Protecting the rare during a rare pandemic," published in 2020 in The Medical Journal of Australia.

  • Protecting the rare during a rare pandemic (2020) - The Medical Journal of Australia

This publication aligns with their noted frequent publication venue:

  • The Medical Journal of Australia

Their collaborative work involves coauthors such as:

  • Gareth Baynam
  • Kaustuv Bhattacharya
  • Nicole Millis

Best Publications

  • Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome

    Heidi Hahn;Carol Wicking;Peter G Zaphiropoulos;Mae R Gailani

  • Medulloblastomas of the desmoplastic variant carry mutations of the human homologue of Drosophila patched

    Torsten Pietsch;Andreas Waha;Anke Koch;Jürgen Kraus

  • Nevoid basal cell carcinoma syndrome: Review of 118 affected individuals

    Susan Shanley;John Ratcliffe;Athel Hockey;Eric Haan

  • Correction: Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

    Miriam Schmidts;Yuqing Hou;Claudio R. Cortes;Dorus A. Mans

  • A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans

    Fan Liu;Fedde van der Lijn;Claudia Schurmann;Gu Zhu

  • Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the patched protein, and no genotype-phenotype correlations are evident

    Carol Wicking;Susan Shanley;Ian Macleod Smyth;Susan Gillies

  • A mammalian patched homolog is expressed in target tissues of sonic hedgehog and maps to a region associated with developmental abnormalities

    Heidi Hahn;Jeffrey Christiansen;Carol Wicking;Peter G. Zaphiropoulos

  • Isolation and Characterization of Human Patched 2 (PTCH2), a Putative Tumour Suppressor Gene in Basal Cell Carcinoma and Medulloblastoma on Chromosome 1p32

    Ian Macleod Smyth;Monica A Narang;Tim Evans;Cornelia Heimann

  • The IFT-A Complex Regulates Shh Signaling through Cilia Structure and Membrane Protein Trafficking

    Karel F. Liem;Alyson Ashe;Mu He;Mu He;Peter Satir

  • The hedgehog signalling pathway in tumorigenesis and development.

    Carol Wicking;Ian Smyth;Allen Bale

  • Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease

    Hao Lu;Maria C Rondón Galeano;Elisabeth Ott;Geraldine Kaeslin

  • Novel genes regulated by Sonic Hedgehog in pluripotent mesenchymal cells.

    Wendy J Ingram;Carol A Wicking;Carol A Wicking;Sean M Grimmond;Alistair Raymond Russell Forrest

  • Murine Wnt-11 and Wnt-12 have temporally and spatially restricted expression patterns during embryonic development

    Jeffrey H. Christiansen;Carina L. Dennis;Carol A. Wicking;Susan J. Monkley

  • Rab23, a negative regulator of hedgehog signaling, localizes to the plasma membrane and the endocytic pathway.

    Timothy M. Evans;Charles Ferguson;Brandon J. Wainwright;Robert G. Parton

  • CDX2, a human homologue of Drosophila caudal, is mutated in both alleles in a replication error positive colorectal cancer

    Carol Wicking;Lisa A Simms;Timothy Evans;Michael Walsh

  • A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development

    Alyson Ashe;Daniel K Morgan;Daniel K Morgan;Nadia C Whitelaw;Nadia C Whitelaw;Timothy J Bruxner

  • Short-Rib Polydactyly and Jeune Syndromes Are Caused by Mutations in WDR60

    Aideen M. McInerney-Leo;Miriam Schmidts;Claudio R. Cortés;Paul J. Leo

  • Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy

    Miriam Schmidts;Julia Vodopiutz;Sonia Christou-Savina;Claudio R. Cortés

  • Attenuated sensing of SHH by Ptch1 underlies evolution of bovine limbs

    Javier Lopez-Rios;Amandine Duchesne;Dario Speziale;Guillaume Andrey

  • ISOLATION OF A HUMAN-GENE WITH PROTEIN-SEQUENCE SIMILARITY TO HUMAN AND MURINE INT-1 AND THE DROSOPHILA SEGMENT POLARITY MUTANT WINGLESS

    B. J. Wainwright;P. J. Scambler;P. Stanier;E. K. Watson

Frequent Co-Authors

Brandon J. Wainwright
Brandon J. Wainwright University of Queensland
Georgia Chenevix-Trench
Georgia Chenevix-Trench QIMR Berghofer Medical Research Institute
Emma L. Duncan
Emma L. Duncan University of Queensland
Matthew A. Brown
Matthew A. Brown Guy's and St Thomas' NHS Foundation Trust
Peter J. Scambler
Peter J. Scambler University College London
Robert G. Parton
Robert G. Parton University of Queensland
Allen E. Bale
Allen E. Bale Yale University
Hannah M. Mitchison
Hannah M. Mitchison University College London
Philip L. Beales
Philip L. Beales University College London
Michael Dean
Michael Dean National Institutes of Health

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