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Profile Details
Contact
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USD 50 /hr
Hire Dr. Herlina Handoko
Australia
USD 50 /hr

Freelance, contract-to-hire, molecular geneticist | Expert in molecular biology techniques at the wet laboratory.

Profile Summary
Subject Matter Expertise
Services
Scientific writing News article
Academic research Internet research, Evidence-based answers, Secondary data compilation, Literature search
Work Experience

Freelance Scientist

Scientist4Hire

November 2019 - Present

Senior Reserach Officer

QIMR Berghofer Medical Research Institute

August 2006 - Present

Queensland Centre for Mental Health Research

2001 - July 2006

Education

PhD

University of Minnesota Twin Cities

- 1995

MSc

University of Minnesota Twin Cities

- 1990

BSc (Biologi)

Universitas Indonesia Fakultas Matematika dan Ilmu Pengetahuan Alam

- 1985

Certifications
  • Certification details not provided.
Publications
JOURNAL ARTICLE
(2017). Keratinocyte Sonic Hedgehog upregulation drives the development of giant congenital nevi via paracrine Endothelin-1 secretion. J Invest Dermatol.
(2016). A mutation in the Cdon gene potentiates congenital nevus development mediated by NRAS(Q61K). Pigment Cell Melanoma Research.
(2013). Plasticity of melanoma in vivo . Pigment Cell & Melanoma Research.
(2012). Modeling epidermal melanoma in mice . Journal of Investigative Dermatology.
(2008). Association of PIP5K2A with schizophrenia . American Journal of Medical Genetics B Neuropsychiatric Genetics.
(2008). Association study of candidate variants of COMT with neuroticism, anxiety and depression . American Journal of Medical Genetics B Neuropsychiatric Genetics.
(2007). SiDCoN. PLoS One.
(2006). Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples. Twin Research and Human Genetics.
(2006). Polymorphisms in the vitamin D receptor and their associations with risk of schizophrenia and selected anthropometric measures. American Journal of Human Biology.
(2006). Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia. Molecular Psychiatry.
(2006). Polimorfisme Adenine Nucleotide Translocator-2 pada populasi individu normal dan Leber's Hereditary Optic Neuropathy. Jurnal Kedokteran Brawijaya.
(2005). Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia. Molecular Psychiatry.
(2003). Tumor necrosis factor haplotype analysis amongst schizophrenia probands from four distinct populations in the Asia-Pacific region. American Journal of Medical Genetics B Neuropsychiatric Genetics.
(2001). Length variations in the COII-tRNA(Lys) intergenic region of mitochondria DNA in Indonesian populations. Human Biology.
(1998). Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy. Journal of Medical Genetics.
(1991). Molecular analysis of an extended family with type IA (tyrosinase-negative) oculocutaneous albinism. Journal of Investigative Dermatology.
(1991). PCR detection of a TaqI polymorphism in the CCAATT box of the human tyrosinase (TYR) gene. Nucleic Acids Research.
BOOK CHAPTER
(2015). Mouse models for actinic keratosis and squamouse cell carcinoma. Current Problems in Dermatology.