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Hire Dr. Herlina H.
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Freelance, contract-to-hire, molecular geneticist | Expert in molecular biology techniques at the wet laboratory.
Subject Matter Expertise
Research Fact Checking, Gray Literature Search, Systematic Literature Review, Secondary Data Collection
November 2019 - Present
Senior Reserach Officer
QIMR Berghofer Medical Research Institute
August 2006 - Present
Queensland Centre for Mental Health Research
2001 - July 2006
University of Minnesota Twin Cities
University of Minnesota Twin Cities
Universitas Indonesia Fakultas Matematika dan Ilmu Pengetahuan Alam
- Certification details not provided.
(2020). Murine dorsal hair type is genetically determined by polymorphisms in candidate genes that influence BMP and WNT signalling . Experimental Dermatology.
(2019). Unexpected High Levels of BRN2/POU3F2 Expression in Human Dermal Melanocytic Nevi . Journal of Investigative Dermatology.
(2019). Different genetic mechanisms mediate spontaneous versus UVR-induced malignant melanoma . eLife.
(2017). Keratinocyte Sonic Hedgehog upregulation drives the development of giant congenital nevi via paracrine Endothelin-1 secretion. J Invest Dermatol.
(2017). Melanocyte transformation requires complete loss of all pocket protein function via a mechanism that mitigates the need for MAPK pathway activation . Oncogene.
(2016). A mutation in the Cdon gene potentiates congenital nevus development mediated by NRAS(Q61K). Pigment Cell Melanoma Research.
(2015). Murine melanomas accelerated by a single UVR exposure carry photoproduct footprints but lack UV signature C>T mutations in critical genes . Oncogene.
(2015). Melanoma susceptibility as a complex trait . Oncogene.
(2015). Lack of evidence from a transgenic mouse model that the activation and migration of melanocytes to the epidermis after neonatal UVR enhances melanoma development . Journal of Investigative Dermatology.
(2015). Hair follicle melanocyte precursors are awoken by ultraviolet radiation via a cell extrinsic mechanism . Photochemical & Photobiological Sciences.
(2014). Differential effects of ultraviolet irradiation in neonatal versus adult mice are not explained by defective macrophage or neutrophil infiltration . Journal of Investigative Dermatology.
(2013). UVB-induced melanocyte proliferation in neonatal mice driven by CCR2-independent recruitment of Ly6clowMHCIIhi macrophages . Journal of Investigative Dermatology.
(2013). Plasticity of melanoma in vivo . Pigment Cell & Melanoma Research.
(2012). Modeling epidermal melanoma in mice . Journal of Investigative Dermatology.
(2011). Superficial spereading-like melanomas in Arf-/-::Tyr-NrasQ61K::K14-Kitl mice . Journal of Investigative Dermatology.
(2010). Differential roles of the pRb and Arf/p53 pathways in murine naevus and melanoma genesis . Pigment Cell & Melanoma Reserach.
(2010). No association between neuregulin 1 and psychotic symptoms in Alzheimer's disease patients . Journal of Alzheimer Disease.
(2008). Association of PIP5K2A with schizophrenia . American Journal of Medical Genetics B Neuropsychiatric Genetics.
(2008). Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression . Psychiatric Genetics.
(2008). Association study of candidate variants of COMT with neuroticism, anxiety and depression . American Journal of Medical Genetics B Neuropsychiatric Genetics.
(2008). Genome-wide scan in 124 Indonesian sib-pair families with schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21 . American Journal of Medical Genetcis B Neurpsychiatric Genetics.
(2008). Genome-wide copy number analysis in esophageal adenocarcinoma using high-density single-nucleotide polymorphism arrays . Cancer Research.
(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.
(2015). Mouse models for actinic keratosis and squamouse cell carcinoma. Current Problems in Dermatology.