| Childhood obesity PW Speiser, MCJ Rudolf, H Anhalt, C Camacho-Hubner, F Chiarelli, ... The journal of clinical endocrinology & metabolism 90 (3), 1871-1887, 2005 | 1137 | 2005 |
| Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletion O Elpeleg, C Miller, E Hershkovitz, M Bitner-Glindzicz, ... The American Journal of Human Genetics 76 (6), 1081-1086, 2005 | 379 | 2005 |
| Autosomal-recessive hypophosphatemic rickets is associated with an inactivation mutation in the ENPP1 gene V Levy-Litan, E Hershkovitz, L Avizov, N Leventhal, D Bercovich, ... The American Journal of Human Genetics 86 (2), 273-278, 2010 | 304 | 2010 |
| Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation C Miller, A Saada, N Shaul, N Shabtai, E Ben‐Shalom, A Shaag, ... Annals of Neurology: Official Journal of the American Neurological …, 2004 | 268 | 2004 |
| Mutation of TBCE causes hypoparathyroidism–retardation–dysmorphism and autosomal recessive Kenny–Caffey syndrome. R Parvari, E Hershkovitz, N Grossman, R Gorodischer, B Loeys, A Zecic, ... Nature genetics 32 (3), 2002 | 255 | 2002 |
| Successful immune tolerance induction to enzyme replacement therapy in CRIM-negative infantile Pompe disease YH Messinger, NJ Mendelsohn, W Rhead, D Dimmock, E Hershkovitz, ... Genetics in medicine 14 (1), 135-142, 2012 | 229 | 2012 |
| Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli‐Bedouins: Genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings … S Shatzky, S Moses, J Levy, V Pinsk, E Hershkovitz, L Herzog, Z Shorer, ... American journal of medical genetics 92 (5), 353-360, 2000 | 157 | 2000 |
| The gene for glycogen-storage disease type 1b maps to chromosome 11q23 B Annabi, BC Mansfield, H Hiraiwa, KJ Lei, T Ubagai, ... The American Journal of Human Genetics 62 (2), 400-405, 1998 | 148 | 1998 |
| Mitochondrial complex I deficiency caused by a deleterious NDUFA11 mutation I Berger, E Hershkovitz, A Shaag, S Edvardson, A Saada, O Elpeleg Annals of neurology 63 (3), 405-408, 2008 | 130 | 2008 |
| Thyroglossal duct carcinoma in children: case presentation and review of the literature A Peretz, E Leiberman, J Kapelushnik, E Hershkovitz Thyroid 14 (9), 777-785, 2004 | 120 | 2004 |
| The utility of basal serum LH in prediction of central precocious puberty in girls Y Pasternak, M Friger, N Loewenthal, A Haim, E Hershkovitz European journal of endocrinology 166 (2), 295-299, 2012 | 119 | 2012 |
| Effects of a twelve-week randomized intervention of exercise and/or diet on weight loss and weight maintenance, and other metabolic parameters in obese preadolescent children S Shalitin, L Ashkenazi-Hoffnung, M Yackobovitch-Gavan, N Nagelberg, ... Hormone Research in Paediatrics 72 (5), 287-301, 2009 | 115 | 2009 |
| The influence of diet and/or exercise and parental compliance on health-related quality of life in obese children M Yackobovitch-Gavan, N Nagelberg, M Phillip, L Ashkenazi-Hoffnung, ... Nutrition Research 29 (6), 397-404, 2009 | 104 | 2009 |
| Homozygous mutation G539R in the gene for P450 oxidoreductase in a family previously diagnosed as having 17, 20-lyase deficiency E Hershkovitz, R Parvari, SA Wudy, MF Hartmann, LG Gomes, ... The Journal of Clinical Endocrinology & Metabolism 93 (9), 3584-3588, 2008 | 102 | 2008 |
| TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome R Spiegel, M Khayat, SA Shalev, Y Horovitz, H Mandel, E Hershkovitz, ... Journal of medical genetics 48 (3), 177-182, 2011 | 85 | 2011 |
| Automated identification of RNA conformational motifs: theory and application to the HM LSU 23S rRNA E Hershkovitz, E Tannenbaum, SB Howerton, A Sheth, A Tannenbaum, ... Nucleic Acids Research 31 (21), 6249-6257, 2003 | 84 | 2003 |
| Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on … R Parvari, E Hershkovitz, A Kanis, R Gorodischer, S Shalitin, VC Sheffield, ... The American Journal of Human Genetics 63 (1), 163-169, 1998 | 79 | 1998 |
| A single-base deletion in the 3′-coding region of glycogen-debranching enzyme is prevalent in glycogen storage disease type IIIA in a population of North African Jewish patients R Parvari, S Moses, J Shen, E Hershkovitz, A Lerner, YT Chen European Journal of Human Genetics 5 (5), 266-270, 1997 | 79 | 1997 |
| Luteinizing hormone-releasing hormone antagonists interfere with autocrine and paracrine growth stimulation of MCF-7 mammary cancer cells by insulin-like growth factors E Hershkovitz, M Marbach, E Bosin, J Levy, CT Roberts Jr, D Leroith, ... The Journal of Clinical Endocrinology & Metabolism 77 (4), 963-968, 1993 | 75 | 1993 |
| A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease R Parvari, I Brodyansky, O Elpeleg, S Moses, D Landau, E Hershkovitz The American Journal of Human Genetics 69 (4), 869-875, 2001 | 74 | 2001 |
