Yisrael Sidis

Author PubWeight™ 47.60‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression. Nat Genet 2006 8.32
2 Modulation of bone morphogenetic protein signaling in vivo regulates systemic iron balance. J Clin Invest 2007 4.09
3 Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice. J Clin Invest 2008 2.69
4 Hemojuvelin regulates hepcidin expression via a selective subset of BMP ligands and receptors independently of neogenin. Blood 2008 2.01
5 Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum. J Clin Endocrinol Metab 2008 1.92
6 DRAGON, a bone morphogenetic protein co-receptor. J Biol Chem 2005 1.89
7 Activins, inhibins, and follistatins: from endocrinology to signaling. A paradigm for the new millennium. Exp Biol Med (Maywood) 2002 1.67
8 Differential biosynthesis and intracellular transport of follistatin isoforms and follistatin-like-3. Endocrinology 2005 1.59
9 FSTL3 deletion reveals roles for TGF-beta family ligands in glucose and fat homeostasis in adults. Proc Natl Acad Sci U S A 2007 1.55
10 Repulsive guidance molecule RGMa alters utilization of bone morphogenetic protein (BMP) type II receptors by BMP2 and BMP4. J Biol Chem 2007 1.45
11 Differential antagonism of activin, myostatin and growth and differentiation factor 11 by wild-type and mutant follistatin. Endocrinology 2008 1.27
12 Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism. Am J Hum Genet 2013 1.26
13 A genetic basis for functional hypothalamic amenorrhea. N Engl J Med 2011 1.24
14 Impaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadism. J Clin Endocrinol Metab 2009 1.22
15 Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia. J Clin Endocrinol Metab 2012 1.18
16 The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations. Endocr Rev 2010 1.16
17 Differential distribution of follistatin isoforms: application of a new FS315-specific immunoassay. J Clin Endocrinol Metab 2004 1.12
18 The role of follistatin domains in follistatin biological action. Mol Endocrinol 2003 1.01
19 Overexpression of follistatin-like 3 in gonads causes defects in gonadal development and function in transgenic mice. Mol Endocrinol 2004 1.00
20 Structure of myostatin·follistatin-like 3: N-terminal domains of follistatin-type molecules exhibit alternate modes of binding. J Biol Chem 2011 1.00
21 The structure of FSTL3.activin A complex. Differential binding of N-terminal domains influences follistatin-type antagonist specificity. J Biol Chem 2008 0.99
22 Klotho coreceptors inhibit signaling by paracrine fibroblast growth factor 8 subfamily ligands. Mol Cell Biol 2012 0.96
23 Differential binding and neutralization of activins A and B by follistatin and follistatin like-3 (FSTL-3/FSRP/FLRG). Endocrinology 2003 0.95
24 Reconstitution and analysis of soluble inhibin and activin receptor complexes in a cell-free system. J Biol Chem 2004 0.95
25 Localization and action of Dragon (repulsive guidance molecule b), a novel bone morphogenetic protein coreceptor, throughout the reproductive axis. Endocrinology 2005 0.93
26 Follistatin and follistatin like-3 differentially regulate adiposity and glucose homeostasis. Obesity (Silver Spring) 2011 0.93
27 The follistatin-288 isoform alone is sufficient for survival but not for normal fertility in mice. Endocrinology 2009 0.90
28 Activin receptor-like kinase-2 inhibits activin signaling by blocking the binding of activin to its type II receptor. J Endocrinol 2007 0.88
29 Differential actions of follistatin and follistatin-like 3. Mol Cell Endocrinol 2004 0.87
30 The puzzles of the prokineticin 2 pathway in human reproduction. Mol Cell Endocrinol 2011 0.79
31 Comparative functional analysis of two fibroblast growth factor receptor 1 (FGFR1) mutations affecting the same residue (R254W and R254Q) in isolated hypogonadotropic hypogonadism (IHH). Gene 2012 0.78
32 Frequency of Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism. Endocr Rev 2009 0.76