| Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy JM Morante-Redolat, A Gorostidi-Pagola, S Piquer-Sirerol, A Sáenz, ... Human molecular genetics 11 (9), 1119-1128, 2002 | 393 | 2002 |
| Beta + thalassemia: aberrant splicing results from a single point mutation in an intron M Busslinger, N Moschonas, F RA Cell 2 (1), 289-298, 1981 | 304 | 1981 |
| neuralized Encodes a Peripheral Membrane Protein Involved in Delta Signaling and Endocytosis E Pavlopoulos, C Pitsouli, KM Klueg, MAT Muskavitch, NK Moschonas, ... Developmental Cell 1 (6), 807-816, 2001 | 295 | 2001 |
| Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families R Michelucci, JJ Poza, V Sofia, MR Feo, S Binelli, F Bisulli, E Scudellaro, ... Epilepsia 44 (10), 1289-1297, 2003 | 186 | 2003 |
| The Complete Maternal and Paternal Mitochondrial Genomes of the Mediterranean Mussel Mytilus galloprovincialis: Implications for the Doubly Uniparental … A Mizi, E Zouros, N Moschonas, GC Rodakis Molecular Biology and Evolution 22 (4), 952-967, 2005 | 173 | 2005 |
| The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders E Staub, J Pérez-Tur, R Siebert, C Nobile, NK Moschonas, P Deloukas, ... Trends in biochemical sciences 27 (9), 441-444, 2002 | 148 | 2002 |
| The DNA sequence and comparative analysis of human chromosome 10 P Deloukas, ME Earthrowl, DV Grafham, M Rubenfield, L French, ... Nature 429 (6990), 375-381, 2004 | 125 | 2004 |
| Isolation and characterization of cDNA clones encoding human liver glutamate dehydrogenase: evidence for a small gene family. G Mavrothalassitis, G Tzimagiorgis, A Mitsialis, V Zannis, A Plaitakis, ... Proceedings of the National Academy of Sciences 85 (10), 3494-3498, 1988 | 122 | 1988 |
| Structure and expression of a cloned β° thalassaemic globin gene N Moschonas, E De Boer, FG Grosveld, HHM Dahl, S Wright, ... Nucleic acids research 9 (17), 4391-4402, 1981 | 100 | 1981 |
| The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X DR Bentley, P Deloukas, A Dunham, L French, SG Gregory, SJ Humphray, ... Nature 409 (6822), 942-943, 2001 | 97 | 2001 |
| Nerve tissue‐specific human glutamate dehydrogenase that is thermolabile and highly regulated by ADP P Shashidharan, DD Clarke, N Ahmed, N Moschonas, A Plaitakis Journal of neurochemistry 68 (5), 1804-1811, 1997 | 95 | 1997 |
| Neuralized-like 1 (Neurl1) targeted to the plasma membrane by N-myristoylation regulates the Notch ligand Jagged1 E Koutelou, S Sato, C Tomomori-Sato, L Florens, SK Swanson, ... Journal of Biological Chemistry 283 (7), 3846-3853, 2008 | 90 | 2008 |
| The human glutamate dehydrogenase gene family: gene organization and structural characterization TM Michaelidis, G Tzimagiorgis, NK Moschonas, J Papamatheakis Genomics 16 (1), 150-160, 1993 | 84 | 1993 |
| The DNA sequence of the 5′ flanking region of the human 0-gk bin gene: evolutionary conservation and polymorphic differences N Maschonas, E de Boer, RA Flavell Nucleic acids research 10 (6), 2109-2120, 1982 | 81 | 1982 |
| Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein T Sarafidou, C Kahl, I Martinez-Garay, M Mangelsdorf, S Gesk, E Baker, ... Genomics 84 (1), 69-81, 2004 | 77 | 2004 |
| Isolation and characterization of a third isoform of human hepatocyte nuclear factor 4 AA Kritis, A Argyrokastritis, NK Moschonas, S Power, N Katrakili, VI Zannis, ... Gene 173 (2), 275-280, 1996 | 76 | 1996 |
| Paleolithic Y-haplogroup heritage predominates in a Cretan highland plateau L Martinez, PA Underhill, LA Zhivotovsky, T Gayden, NK Moschonas, ... European Journal of Human Genetics 15 (4), 485-493, 2007 | 64 | 2007 |
| Sequences Located 3′ to the Breakpoint of the Hereditary Persistence of Fetal Hemoglobin-3 Deletion Exhibit Enhancer Activity and Can Modify the Developmental Expression of … NP Anagnou, C Perez-Stable, G Gelinas, C Costantini, L Liapaki, ... Journal of Biological Chemistry 270 (17), 10256-10263, 1995 | 59 | 1995 |
| PICKLE 2.0: A human protein-protein interaction meta-database employing data integration via genetic information ontology A Gioutlakis, MI Klapa, NK Moschonas PloS one 12 (10), e0186039, 2017 | 58 | 2017 |
| Detection and incidence of cryptic Y chromosome sequences in Turner syndrome patients PC Patsalis, C Sismani, MI Hadjimarcou, S Kitsiou‐Tzeli, A Tzezou, ... Clinical genetics 53 (4), 249-257, 1998 | 44 | 1998 |
Richard A. FlavellSterling Professor of Immunobiology, Yale University, HHMI InvestigatorVerified email at yale.edu
