Debora Rapaport

1.9k total citations
30 papers, 1.2k citations indexed

About

Debora Rapaport is a scholar working on Molecular Biology, Cell Biology and Physiology. According to data from OpenAlex, Debora Rapaport has authored 30 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 16 papers in Cell Biology and 9 papers in Physiology. Recurrent topics in Debora Rapaport's work include Muscle Physiology and Disorders (15 papers), Cellular transport and secretion (10 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Debora Rapaport is often cited by papers focused on Muscle Physiology and Disorders (15 papers), Cellular transport and secretion (10 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Debora Rapaport collaborates with scholars based in Israel, Brazil and United States. Debora Rapaport's co-authors include Mia Horowitz, Maria Rita Passos‐Bueno, Mariz Vainzof, Steve Caplan, Naava Naslavsky, Mayana Zatz, Eli Sprecher, Mayana Zatz, Marko Jović and Rita de Cássia M. Pavanello and has published in prestigious journals such as PLoS ONE, Journal of Virology and Biochemical Journal.

In The Last Decade

Debora Rapaport

30 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Debora Rapaport Israel 19 805 439 235 142 140 30 1.2k
Serge A. Leibovitch France 22 1.4k 1.8× 334 0.8× 267 1.1× 209 1.5× 101 0.7× 57 1.7k
Denise Paulin France 11 1.3k 1.6× 666 1.5× 105 0.4× 172 1.2× 249 1.8× 11 1.6k
Teresa Occhiodoro Australia 12 577 0.7× 130 0.3× 260 1.1× 146 1.0× 138 1.0× 14 937
Stefano Regis Italy 22 1.2k 1.5× 317 0.7× 521 2.2× 169 1.2× 114 0.8× 57 1.9k
Sue Shackleton United Kingdom 16 1.8k 2.2× 471 1.1× 132 0.6× 128 0.9× 122 0.9× 24 2.0k
Muriel Vernet France 15 980 1.2× 407 0.9× 61 0.3× 176 1.2× 147 1.1× 20 1.4k
Michael Lindenbaum Canada 10 1.3k 1.6× 418 1.0× 262 1.1× 166 1.2× 76 0.5× 11 1.6k
Terri G. Thompson United States 13 891 1.1× 271 0.6× 99 0.4× 156 1.1× 331 2.4× 15 1.2k
Jaime Meléndez Chile 16 734 0.9× 278 0.6× 79 0.3× 113 0.8× 387 2.8× 25 1.3k

Countries citing papers authored by Debora Rapaport

Since Specialization
Citations

This map shows the geographic impact of Debora Rapaport's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Debora Rapaport with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Debora Rapaport more than expected).

Fields of papers citing papers by Debora Rapaport

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Debora Rapaport. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Debora Rapaport. The network helps show where Debora Rapaport may publish in the future.

Co-authorship network of co-authors of Debora Rapaport

This figure shows the co-authorship network connecting the top 25 collaborators of Debora Rapaport. A scholar is included among the top collaborators of Debora Rapaport based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Debora Rapaport. Debora Rapaport is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Maor, Gali, Debora Rapaport, & Mia Horowitz. (2019). The effect of mutant GBA1 on accumulation and aggregation of α-synuclein. Human Molecular Genetics. 28(11). 1768–1781. 36 indexed citations
2.
Rapaport, Debora, et al.. (2014). Parkin-mediated ubiquitination of mutant glucocerebrosidase leads to competition with its substrates PARIS and ARTS. Orphanet Journal of Rare Diseases. 9(1). 86–86. 25 indexed citations
3.
Sarig, Ofer, Debora Rapaport, Akemi Ishida‐Yamamoto, et al.. (2012). Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Syndrome Is Caused by a POC1A Mutation. The American Journal of Human Genetics. 91(2). 337–342. 53 indexed citations
4.
Rapaport, Debora, et al.. (2010). Loss of SNAP29 Impairs Endocytic Recycling and Cell Motility. PLoS ONE. 5(3). e9759–e9759. 53 indexed citations
5.
Fichtman, Boris, et al.. (2008). EHDS are serine phosphoproteins: EHD1 phosphorylation is enhanced by serum stimulation. Cellular & Molecular Biology Letters. 13(4). 632–48. 7 indexed citations
6.
Naslavsky, Naava, Juliati Rahajeng, Debora Rapaport, Mia Horowitz, & Steve Caplan. (2007). EHD1 regulates cholesterol homeostasis and lipid droplet storage. Biochemical and Biophysical Research Communications. 357(3). 792–799. 39 indexed citations
7.
Sprecher, Eli, Akemi Ishida‐Yamamoto, Debora Rapaport, et al.. (2005). A Mutation in SNAP29, Coding for a SNARE Protein Involved in Intracellular Trafficking, Causes a Novel Neurocutaneous Syndrome Characterized by Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma. The American Journal of Human Genetics. 77(2). 242–251. 131 indexed citations
8.
Rapaport, Debora, et al.. (1998). The DNA Sequence of the RK Strain of Human Herpesvirus 7. Virology. 244(1). 119–132. 68 indexed citations
9.
Rapaport, Debora, David Greenberg, Michael Tal, David Yaffe, & Uri Nudel. (1993). Dp71, the nonmuscle product of the Duchenne muscular dystrophy gene is associated with the cell membrane. FEBS Letters. 328(1-2). 197–202. 34 indexed citations
10.
Rapaport, Debora, Doron Lederfein, Johan T. den Dunnen, et al.. (1992). Characterization and cell type distribution of a novel, major transcript of the Duchenne Muscular Dystrophy gene. Differentiation. 49(3). 187–193. 62 indexed citations
11.
12.
Passos‐Bueno, Maria Rita, Barbara C. Byth, Donald R. Love, et al.. (1991). Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27. Journal of the Neurological Sciences. 102(2). 206–208. 1 indexed citations
13.
Zatz, Mayana, Debora Rapaport, Mariz Vainzof, et al.. (1991). Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy. Journal of the Neurological Sciences. 102(2). 190–196. 117 indexed citations
14.
Vainzof, Mariz, Rita C.M. Pavanello, Debora Rapaport, et al.. (1991). Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies. American Journal of Medical Genetics. 39(1). 38–41. 16 indexed citations
15.
Zatz, Mayana, Maria Rita Passos‐Bueno, Debora Rapaport, & Mariz Vainzof. (1991). Familial occurrence of Duchenne dystrophy through paternal lines in four families. American Journal of Medical Genetics. 38(1). 80–84. 9 indexed citations
16.
Rapaport, Debora, et al.. (1991). Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy. American Journal of Medical Genetics. 39(4). 437–441. 58 indexed citations
17.
Vainzof, Mariz, et al.. (1990). Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian study. Journal of the Neurological Sciences. 98(2-3). 221–233. 32 indexed citations
18.
Zatz, Mayana, et al.. (1989). Nocturnal rhythm of growth hormone in Duchenne patients: Effect of different doses of mazindol and/or cyproheptadine. American Journal of Medical Genetics. 33(4). 457–467. 7 indexed citations
19.
Zatz, Mayana, Debora Rapaport, Mariz Vainzof, et al.. (1988). Relation between height and clinical course in Duchenne muscular dystrophy. American Journal of Medical Genetics. 29(2). 405–410. 20 indexed citations
20.
Rapaport, Debora, G M D D Colletto, Mayana Zatz, John M. Opitz, & James F. Reynolds. (1988). Genetic and environmental components of serum creatine kinase (CK) and pyruvate kinase (PK) in normal twins: Implication for genetic risks estimates in Duchenne muscular dystrophy carriers. American Journal of Medical Genetics. 31(2). 291–298. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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