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1,821 authors found
quering by "DYRK1A"
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the first 25
sort by ONE Index.
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934
One Index
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Gutierrez, Maximiliano PhD 0000-0003-3199-0337 |
128 docs (2002 - 2024)
Mycobacterium tuberculosis , Intracellular parasite , Rab , Phagolysosome , Bedaquiline |
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917
One Index
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Wiest, Olaf PhD 0000-0001-9316-7720 |
286 docs (1990 - 2024)
Crystal Structures , Continuous Crystallization , Structure Determination , Crystallography , Ultrasound-Assisted Crystallization |
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908
One Index
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Plagnol, Vincent PhD 0000-0002-5597-9215 |
311 docs (2003 - 2024)
Genome-wide association study , Genetic association , Exome , Liquid biopsy , Type 1 Diabetes |
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903
One Index
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Kim, Eunjoon PhD 0000-0001-5518-6584 |
291 docs (1988 - 2024)
Postsynaptic density , Synaptic Plasticity , PDZ domain , Autism , Excitatory synapse |
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903
One Index
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Di Domenico, Fabio PhD 0000-0002-2013-209X |
163 docs (2008 - 2024)
Neuropathology , Neurodegeneration , Biliverdin reductase , Protein Misfolding , Proteostasis |
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888
One Index
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Fisher, Elizabeth PhD 0000-0003-2850-9936 |
671 docs (1965 - 2024)
Neurodegeneration , Trisomy , Chromosome 21 , Apolipoprotein E , Amyloid (mycology) |
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886
One Index
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Iannacone, Matteo PhD 0000-0002-9370-2671 |
170 docs (2001 - 2024)
Memory T Cells , Pathogenesis , T Cell Immunity , Priming (agriculture) , CTL* |
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885
One Index
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Yaari, Gur PhD 0000-0001-9311-9884 |
143 docs (2004 - 2024)
IGHV@ , Antibody Repertoire , Thymic Selection , Immune Tolerance , Immunological Surveillance |
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881
One Index
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Mignot, Cyril PhD 0000-0002-3462-3463 |
589 docs (1984 - 2024)
Microcephaly , Brain Development , Neurodevelopmental disorder , Haploinsufficiency , Exome Sequencing |
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880
One Index
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Krantz, Ian PhD 0000-0003-2442-1128 |
298 docs (1980 - 2024)
Alagille Syndrome , JAG1 , Proband , Haploinsufficiency , Table (database) |
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879
One Index
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Isidor, Bertrand PhD 0000-0001-6480-126X |
485 docs (1991 - 2024)
Haploinsufficiency , Microcephaly , Neurodevelopmental disorder , Loss function , Brain Development |
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874
One Index
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Jansen-Duerr, Pidder PhD 0000-0001-7771-3429 |
223 docs (1988 - 2024)
Senescence , Aging , E2F , Cyclin A , NOX4 |
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870
One Index
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Mirzaa, Ghayda PhD 0000-0003-2648-7657 |
172 docs (2004 - 2024)
Megalencephaly , Microcephaly , Polymicrogyria , Neurodevelopmental disorder , Brain Development |
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870
One Index
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Scaglia, Fernando PhD 0000-0003-3502-8460 |
252 docs (1998 - 2024)
Inborn Errors of Metabolism , Mitochondrial disease , Mitochondrial Dysfunction , Mitochondrial Function , Mitochondria |
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870
One Index
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Mandel, Jean Louis PhD 0000-0002-0535-6589 |
522 docs (1933 - 2024)
Fragile X Syndrome , Genetic linkage , Adrenoleukodystrophy , Xq28 , FMR1 |
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865
One Index
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Arron, Joseph PhD 0000-0001-7677-9979 |
171 docs (1996 - 2024)
Asthma , Periostin , Type 2 Immunity , Treatment , Interleukin 13 |
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864
One Index
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DeCaprio, James PhD 0000-0002-0896-167X |
264 docs (1988 - 2024)
Merkel cell polyomavirus , Merkel Cell Carcinoma , Retinoblastoma protein , E2F , Merkel cell |
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864
One Index
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Christine M. Eng PhD 0009-0008-8627-8228 |
242 docs (1991 - 2024)
Exome , Exome Sequencing , Fetal DNA Analysis , Proband , Haploinsufficiency |
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862
One Index
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Knapp, Stefan PhD 0000-0001-5995-6494 |
758 docs (1974 - 2024)
BET Bromodomains , Crystal (programming language) , BRD4 , Protein kinase domain , Kinome |
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860
One Index
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Josselin, Beatrice PhD |
23 docs (2019 - 2024)
DYRK1A , Quinazoline , IC50 , Docking (animal) , Structure–activity relationship |
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860
One Index
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Iqbal, Khalid PhD 0000-0002-7670-9580 |
513 docs (1972 - 2024)
Tau protein , Hyperphosphorylation , Tau Pathology , Protein Misfolding , Neurodegeneration |
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858
One Index
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Al-Gazali, Lihadh PhD 0000-0003-2029-2218 |
260 docs (1988 - 2023)
Microcephaly , Joubert syndrome , Exome , Haploinsufficiency , Loss function |
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858
One Index
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De Windt, Leon PhD 0000-0002-7793-2856 |
211 docs (1997 - 2024)
Pressure overload , Cardiac Hypertrophy , NFAT , MicroRNAs , Cardiac Remodeling |
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858
One Index
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Sarazin, Marie PhD 0000-0002-5438-8392 |
243 docs (1995 - 2024)
Alzheimer's Disease , Neuroimaging , Amyloid (mycology) , Posterior cortical atrophy , Neurodegeneration |
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858
One Index
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Thevenon, Julien PhD 0000-0001-9271-3961 |
280 docs (2001 - 2024)
Exome Sequencing , Microcephaly , Exome , Haploinsufficiency , Compound heterozygosity |
