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M. Dinger · SciRah

Researcher profile · Semantic Scholar

M. Dinger

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M. Dinger — researcher profile on SciRah

h-index: 63
Works: 202
Citations: 27K

Most-cited papers

I-motif DNA structures are formed in the nuclei of human cells
Mahdi Zeraati, D. Langley, P. Schofield, Aaron L. Moye +5 more
2018Nature Chemistry472 citations
Semantic Scholar
Evidence that TLR4 Is Not a Receptor for Saturated Fatty Acids but Mediates Lipid-Induced Inflammation by Reprogramming Macrophage Metabolism.
G. Lancaster, Katherine G. Langley, Nils A. Berglund, H. Kammoun +17 more
2018Cell Metabolism417 citations Open access
Semantic Scholar
Benchmarking of RNA-sequencing analysis workflows using whole-transcriptome RT-qPCR expression data
Celine Everaert, Manuel Luypaert, J. Maag, Quek Xiu Cheng +3 more
2017Scientific Reports350 citations Open access
Semantic Scholar
RNAcentral: a hub of information for non-coding RNA sequences
B. Sweeney, Anton I. Petrov, Boris Burkov, R. Finn +57 more
2018Nucleic Acids Res.320 citations Open access
Semantic Scholar
Overcoming challenges and dogmas to understand the functions of pseudogenes
S. Cheetham, G. Faulkner, M. Dinger
2019Nature reviews genetics215 citations
Semantic Scholar
CCR6 Defines Memory B Cell Precursors in Mouse and Human Germinal Centers, Revealing Light‐Zone Location and Predominant Low Antigen Affinity
Suan Dan, N. Krautler, J. Maag, Danyal Butt +10 more
2017Immunity215 citations Open access
Semantic Scholar
Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disorders
L. Ewans, D. Schofield, Rupendra T. Shrestha, Ying Zhu +19 more
2018Genetics in Medicine210 citations Open access
Semantic Scholar
Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy.
R. Bagnall, J. Ingles, M. Dinger, M. Cowley +10 more
2018Journal of the American College of Cardiology172 citations Open access
Semantic Scholar
Universal alternative splicing of noncoding exons
Ira W. Deveson, M. Brunck, J. Blackburn, Elizabeth Tseng +8 more
2017bioRxiv144 citations Open access
Semantic Scholar
A mild PUM1 mutation is associated with adult-onset ataxia, whereas haploinsufficiency causes developmental delay and seizures
Vincenzo A. Gennarino, E. Palmer, Laura M McDonell, Li Wang +37 more
2018Cell130 citations Open access
Semantic Scholar
The regulatory role of long noncoding RNAs in cancer.
Ying Tang, B. Cheung, Bernard Atmadibrata, G. Marshall +3 more
2017Cancer Letters116 citations Open access
Semantic Scholar
Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis
L. Ewans, A. Minoche, Deborah Schofield, R. Shrestha +31 more
2022European Journal of Human Genetics103 citations Open access
Semantic Scholar
Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness
E. Palmer, D. Schofield, Rupendra T. Shrestha, T. Kandula +22 more
2018Molecular Genetics & Genomic Medicine101 citations Open access
Semantic Scholar
Realizing the significance of noncoding functionality in clinical genomics
B. Gloss, M. Dinger
2018Experimental and Molecular Medicine98 citations Open access
Semantic Scholar
The long non-coding RNA NEAT1 is responsive to neuronal activity and is associated with hyperexcitability states
G. Barry, James A. Briggs, D. Hwang, S. Nayler +26 more
2017Scientific Reports98 citations Open access
Semantic Scholar
The long noncoding RNA lncNB1 promotes tumorigenesis by interacting with ribosomal protein RPL35
Pei Y. Liu, Andrew E. Tee, G. Milazzo, K. Hannan +31 more
2019Nature Communications86 citations Open access
Semantic Scholar
Long Noncoding RNAs CUPID1 and CUPID2 Mediate Breast Cancer Risk at 11q13 by Modulating the Response to DNA Damage.
Joshua A. Betts, M. Moradi Marjaneh, F. Al-Ejeh, Y. Lim +27 more
2017American Journal of Human Genetics82 citations Open access
Semantic Scholar
Diagnostic Yield of Whole Genome Sequencing After Nondiagnostic Exome Sequencing or Gene Panel in Developmental and Epileptic Encephalopathies
E. Palmer, R. Sachdev, R. Macintosh, U. S. Melo +24 more
2021Neurology74 citations Open access
Semantic Scholar
Lipid Uptake Is an Androgen-Enhanced Lipid Supply Pathway Associated with Prostate Cancer Disease Progression and Bone Metastasis
K. Tousignant, A. Rockstroh, Atefeh Taherian Fard, M. Lehman +7 more
2019Molecular Cancer Research74 citations Open access
Semantic Scholar
Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare.
Zornitza Stark, Tiffany F. Boughtwood, Matilda A. Haas, J. Braithwaite +54 more
2023American Journal of Human Genetics64 citations Open access
Semantic Scholar
Denisovan, modern human and mouse TNFAIP3 alleles tune A20 phosphorylation and immunity
N. Zammit, O. Siggs, P. Gray, Keisuke Horikawa +52 more
2019Nature Immunology64 citations Open access
Semantic Scholar
The Medical Genome Reference Bank contains whole genome and phenotype data of 2570 healthy elderly
M. Pinese, P. Lacaze, E. Rath, Andrew Stone +34 more
2020Nature Communications63 citations Open access
Semantic Scholar
Intergenic disease-associated regions are abundant in novel transcripts
N. Bartonicek, M. Clark, X. Quek, J. Torpy +10 more
2017Genome Biology62 citations Open access
Semantic Scholar
Non-coding RNAs modulate function of extracellular matrix proteins.
Nader Akbari Dilmaghnai, H. Shoorei, G. Sharifi, Mahdi Mohaqiq +4 more
2021Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie61 citations Open access
Semantic Scholar
ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data
A. Minoche, Ben Lundie, G. Peters, T. Ohnesorg +9 more
2020Genome Medicine59 citations Open access
Semantic Scholar
Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing
A. Mallawaarachchi, Ben Lundie, Y. Hort, N. Schonrock +16 more
2021European Journal of Human Genetics56 citations Open access
Semantic Scholar
Whole genome sequencing provides better diagnostic yield and future value than whole exome sequencing
J. Mattick, M. Dinger, N. Schonrock, M. Cowley
2018Medical Journal of Australia56 citations
Semantic Scholar
Revealing hidden genetic diagnoses in the ocular anterior segment disorders
Alan Ma, S. Yousoof, J. Grigg, M. Flaherty +25 more
2020Genetics in Medicine53 citations Open access
Semantic Scholar
Novel Aberrations Uncovered in Barrett's Esophagus and Esophageal Adenocarcinoma Using Whole Transcriptome Sequencing
J. Maag, Oliver M. Fisher, A. Levert-Mignon, D. Kaczorowski +8 more
2017Molecular Cancer Research52 citations Open access
Semantic Scholar
Machine learning annotation of human branchpoints
Bethany Signal, B. Gloss, M. Dinger, T. Mercer
2018Bioinform.51 citations Open access
Semantic Scholar
Exploring the Role of Non-Coding RNAs in the Pathophysiology of Systemic Lupus Erythematosus
M. Taheri, Reyhane Eghtedarian, M. Dinger, S. Ghafouri-Fard
2020Biomolecules47 citations Open access
Semantic Scholar
Human genomic DNA is widely interspersed with i-motif structures
C. D. Peña Martinez, Mahdi Zeraati, R. Rouet, Ohan Mazigi +14 more
2022bioRxiv46 citations Open access
Semantic Scholar
Whole-Genome Sequencing as a First-Line Genetic Test in Familial Dilated Cardiomyopathy
A. Minoche, C. Horvat, Renee Johnson, V. Gayevskiy +13 more
2018Genetics in Medicine44 citations Open access
Semantic Scholar
Destination Amyotrophic Lateral Sclerosis
Matt Keon, Benjamin Musrie, M. Dinger, S. Brennan +2 more
2021Frontiers in Neurology43 citations Open access
Semantic Scholar
Aberrant RAG-mediated recombination contributes to multiple structural rearrangements in lymphoid blast crisis of chronic myeloid leukemia
D. Thomson, N. Shahrin, Paul P. S. Wang, C. Wadham +6 more
2020Leukemia41 citations
Semantic Scholar
Cancer-associated noncoding mutations affect RNA G-quadruplex-mediated regulation of gene expression
Mahdi Zeraati, Aaron L. Moye, Jason W. H. Wong, Dilmi Perera +4 more
2017Scientific Reports41 citations Open access
Semantic Scholar
Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis
R. Davis, K. Kumar, C. Puttick, Christina Liang +11 more
2022Neurology40 citations Open access
Semantic Scholar
A de novo mutation in the Sodium-Activated Potassium channel KCNT2 alters ion selectivity and causes epileptic encephalopathy
Sushmitha Gururaj, E. Palmer, Garrett D. Sheehan, T. Kandula +14 more
2017Cell Reports40 citations Open access
Semantic Scholar
RNA-seq reveals more consistent reference genes for gene expression studies in human non-melanoma skin cancers
V. Hoang, L. Tom, X. Quek, Jean-Marie Tan +9 more
2017PeerJ40 citations Open access
Semantic Scholar
Dysregulation of non-coding RNAs in Rheumatoid arthritis.
M. Taheri, Reyhane Eghtedarian, M. Dinger, S. Ghafouri-Fard
2020Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie38 citations Open access
Semantic Scholar
Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care
Zornitza Stark, A. Nisselle, B. McClaren, Fiona Lynch +11 more
2019European Journal of Human Genetics38 citations Open access
Semantic Scholar
Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumours.
S. D. De Sousa, M. McCabe, Kathy Wu, T. Roscioli +10 more
2017European Journal of Endocrinology36 citations Open access
Semantic Scholar
LncRNAs and miRNAs participate in determination of response of cancer cells to cisplatin.
M. Taheri, H. Shoorei, Farhad Tondro Anamag, S. Ghafouri-Fard +1 more
2021Experimental and molecular pathology (Print)35 citations
Semantic Scholar
Pathogenic variants in PLOD3 result in a Stickler syndrome-like connective tissue disorder with vascular complications
L. Ewans, A. Colley, C. Gaston-Massuet, A. Gualtieri +16 more
2019Journal of Medical Genetics35 citations Open access
Semantic Scholar
Initiating an undiagnosed diseases program in the Western Australian public health system
G. Baynam, S. Broley, Alicia Bauskis, N. Pachter +39 more
2017Orphanet Journal of Rare Diseases34 citations Open access
Semantic Scholar
Seave: a comprehensive web platform for storing and interrogating human genomic variation
V. Gayevskiy, T. Roscioli, M. Dinger, M. Cowley
2018bioRxiv33 citations Open access
Semantic Scholar
Mutations in the exocyst component EXOC2 cause severe defects in human brain development
N. V. Van Bergen, Syed Mukhtar Ahmed, F. Collins, M. Cowley +15 more
2020Journal of Experimental Medicine32 citations Open access
Semantic Scholar
Equitable Expanded Carrier Screening Needs Indigenous Clinical and Population Genomic Data.
S. Easteal, R. Arkell, Renzo F. Balboa, S. Bellingham +37 more
2020American Journal of Human Genetics31 citations Open access
Semantic Scholar
The critical roles of lncRNAs in the pathogenesis of melanoma.
A. Safa, Mahdi Gholipour, M. Dinger, M. Taheri +1 more
2020Experimental and molecular pathology (Print)31 citations
Semantic Scholar
The Medical Genome Reference Bank: a whole-genome data resource of 4000 healthy elderly individuals. Rationale and cohort design
P. Lacaze, M. Pinese, W. Kaplan, Andrew Stone +6 more
2018bioRxiv31 citations Open access
Semantic Scholar

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