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| Symbol nomenclature for graphical representations of glycans A Varki, RD Cummings, M Aebi, NH Packer, PH Seeberger, JD Esko, ... Glycobiology 25 (12), 1323-1324, 2015 | 1021 | 2015 |
| Lysosomal protease pathways to apoptosis: cleavage of Bid, not pro-caspases, is the most likely route V Stoka, B Turk, SL Schendel, TH Kim, T Cirman, SJ Snipas, LM Ellerby, ... Journal of Biological Chemistry 276 (5), 3149-3157, 2001 | 872 | 2001 |
| Proinflammatory S100 proteins regulate the accumulation of myeloid-derived suppressor cells P Sinha, C Okoro, D Foell, HH Freeze, S Ostrand-Rosenberg, ... The Journal of Immunology 181 (7), 4666-4675, 2008 | 856 | 2008 |
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| RAGE, carboxylated glycans and S100A8/A9 play essential roles in colitis-associated carcinogenesis O Turovskaya, D Foell, P Sinha, T Vogl, R Newlin, J Nayak, M Nguyen, ... Carcinogenesis 29 (10), 2035-2043, 2008 | 381 | 2008 |
| Endogenous damage-associated molecular pattern molecules at the crossroads of inflammation and cancer G Srikrishna, HH Freeze Neoplasia 11 (7), 615-628, 2009 | 353 | 2009 |
| Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder X Wu, RA Steet, O Bohorov, J Bakker, J Newell, M Krieger, L Spaapen, ... Nature medicine 10 (5), 518-523, 2004 | 343 | 2004 |
| Correction of leukocyte adhesion deficiency type II with oral fucose T Marquardt, K Lühn, G Srikrishna, HH Freeze, E Harms, D Vestweber Blood, The Journal of the American Society of Hematology 94 (12), 3976-3985, 1999 | 328 | 1999 |
| SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder V Cantagrel, DJ Lefeber, BG Ng, Z Guan, JL Silhavy, SL Bielas, L Lehle, ... Cell 142 (2), 203-217, 2010 | 319 | 2010 |
| Altered glycan structures: the molecular basis of congenital disorders of glycosylation HH Freeze, M Aebi Current opinion in structural biology 15 (5), 490-498, 2005 | 310 | 2005 |
| Multiple phenotypes in phosphoglucomutase 1 deficiency LC Tegtmeyer, S Rust, M van Scherpenzeel, BG Ng, ME Losfeld, S Timal, ... New England Journal of Medicine 370 (6), 533-542, 2014 | 292 | 2014 |
| Solving glycosylation disorders: fundamental approaches reveal complicated pathways HH Freeze, JX Chong, MJ Bamshad, BG Ng The American Journal of Human Genetics 94 (2), 161-175, 2014 | 290 | 2014 |
| Symbol nomenclature for glycan representation A Varki, RD Cummings, JD Esko, HH Freeze, P Stanley, JD Marth, ... Proteomics 9 (24), 5398-5399, 2009 | 276 | 2009 |
| GLUT14, a duplicon of GLUT3, is specifically expressed in testis as alternative splice forms X Wu, HH Freeze Genomics 80 (6), 553-557, 2002 | 253 | 2002 |
| Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment Y Zhang, X Yu, M Ichikawa, JJ Lyons, S Datta, IT Lamborn, H Jing, ES Kim, ... Journal of Allergy and Clinical Immunology 133 (5), 1400-1409. e5, 2014 | 251 | 2014 |
| Neurological aspects of human glycosylation disorders HH Freeze, EA Eklund, BG Ng, MC Patterson Annual review of neuroscience 38 (1), 105-125, 2015 | 245 | 2015 |
