Hanna Shalev

2.6k total citations
43 papers, 1.5k citations indexed

About

Hanna Shalev is a scholar working on Molecular Biology, Hematology and Physiology. According to data from OpenAlex, Hanna Shalev has authored 43 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Hematology and 16 papers in Physiology. Recurrent topics in Hanna Shalev's work include Erythrocyte Function and Pathophysiology (16 papers), Hemoglobinopathies and Related Disorders (13 papers) and Iron Metabolism and Disorders (8 papers). Hanna Shalev is often cited by papers focused on Erythrocyte Function and Pathophysiology (16 papers), Hemoglobinopathies and Related Disorders (13 papers) and Iron Metabolism and Disorders (8 papers). Hanna Shalev collaborates with scholars based in Israel, United States and France. Hanna Shalev's co-authors include Daniel Landau, Rivka Carmi, Hannah Tamary, Val C. Sheffield, Gretel Beck, Melanie Barbara Boettger, Μαρία Τσολιά, Richard Englehardt, Peter Meyer and Roxanne Y. Walder and has published in prestigious journals such as Nature Genetics, Blood and Brain.

In The Last Decade

Hanna Shalev

43 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hanna Shalev Israel 18 475 468 313 281 270 43 1.5k
Pieter J. Oort United States 12 468 1.0× 98 0.2× 777 2.5× 374 1.3× 238 0.9× 14 1.5k
B Nabarra France 19 317 0.7× 140 0.3× 105 0.3× 99 0.4× 57 0.2× 63 1.4k
Silke Haerteis Germany 21 881 1.9× 138 0.3× 101 0.3× 138 0.5× 111 0.4× 62 1.6k
Hiroo Niimi Japan 24 463 1.0× 195 0.4× 81 0.3× 182 0.6× 34 0.1× 101 1.7k
Pascale Fanen France 26 764 1.6× 82 0.2× 93 0.3× 167 0.6× 329 1.2× 93 2.1k
Hyeyoung Nam United States 15 326 0.7× 454 1.0× 462 1.5× 71 0.3× 415 1.5× 30 1.2k
Brian Pedersen United States 17 504 1.1× 58 0.1× 800 2.6× 78 0.3× 243 0.9× 30 1.8k
Saı̈d Lyoumi France 21 676 1.4× 132 0.3× 223 0.7× 132 0.5× 150 0.6× 30 1.2k
Jeremy Turner United Kingdom 20 939 2.0× 44 0.1× 94 0.3× 114 0.4× 46 0.2× 44 1.6k
Johan Sällström Sweden 22 431 0.9× 62 0.1× 47 0.2× 169 0.6× 95 0.4× 52 1.2k

Countries citing papers authored by Hanna Shalev

Since Specialization
Citations

This map shows the geographic impact of Hanna Shalev'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 Hanna Shalev with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hanna Shalev more than expected).

Fields of papers citing papers by Hanna Shalev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hanna Shalev. 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 Hanna Shalev. The network helps show where Hanna Shalev may publish in the future.

Co-authorship network of co-authors of Hanna Shalev

This figure shows the co-authorship network connecting the top 25 collaborators of Hanna Shalev. A scholar is included among the top collaborators of Hanna Shalev 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 Hanna Shalev. Hanna Shalev 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.
Halpérin, Daniel, Yuval Yogev, Ohad Wormser, et al.. (2019). A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I. Annals of Human Genetics. 83(5). 361–366. 5 indexed citations
2.
Gülsüner, Süleyman, Sarah B. Pierce, Hanna Shalev, et al.. (2018). Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE). Human Molecular Genetics. 28(1). 133–142. 32 indexed citations
3.
Perez, Yonatan, Zamir Shorer, Pauline Chabosseau, et al.. (2017). SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome. Brain. 140(4). 928–939. 71 indexed citations
4.
Dinour, Dganit, Nicola K. Gray, Liat Ganon, et al.. (2011). Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2. Nephrology Dialysis Transplantation. 27(3). 1035–1041. 42 indexed citations
5.
Schreiber, Ruth, Marie-Claire Gübler, Olivier Gribouval, Hanna Shalev, & Daniel Landau. (2010). Inherited renal tubular dysgenesis may not be universally fatal. Pediatric Nephrology. 25(12). 2531–2534. 19 indexed citations
6.
7.
Landau, Daniel, et al.. (2007). Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations. Pediatric Nephrology. 22(5). 661–669. 14 indexed citations
8.
Landau, Daniel, et al.. (2006). Transient severe metastatic calcification in acute renal failure. Pediatric Nephrology. 22(4). 607–611. 7 indexed citations
9.
Shalev, Hanna, et al.. (2006). Murine typhus is a common cause of febrile illness in Bedouin children in Israel. Scandinavian Journal of Infectious Diseases. 38(6-7). 451–455. 17 indexed citations
10.
Basel‐Vanagaite, Lina, Rachel Straussberg, Metsada Pasmanik‐Chor, et al.. (2006). Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis. Annals of Neurology. 60(2). 214–222. 92 indexed citations
11.
Landau, Daniella, David Cohen, Hanna Shalev, et al.. (2004). A novel mutation in the SLC17A5 gene causing both severe and mild phenotypes of free sialic acid storage disease in one inbred Bedouin kindred. Molecular Genetics and Metabolism. 82(2). 167–172. 14 indexed citations
12.
Finer, Gal, Hanna Shalev, Ohad S. Birk, et al.. (2003). Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome. The Journal of Pediatrics. 142(3). 318–323. 67 indexed citations
13.
Walder, Roxanne Y., Daniel Landau, Peter Meyer, et al.. (2002). Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia. Nature Genetics. 31(2). 171–174. 407 indexed citations
14.
Mazor, Dalia, Joseph Kapelushnik, Hanna Shalev, & Naomi Meyerstein. (2001). Possible oxidative stress involvement in congenital dyserythropoietic anemia type 1. The Hematology Journal. 2(3). 196–199. 2 indexed citations
15.
Landau, Daniel, et al.. (2000). Oligohydramnion, renal failure and no pulmonary hypoplasia in glomerulocystic kidney disease. Pediatric Nephrology. 14(4). 319–321. 5 indexed citations
16.
Shalev, Hanna, Asher Moser, Joseph Kapelushnik, et al.. (2000). Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newborn. The Journal of Pediatrics. 136(4). 553–555. 17 indexed citations
17.
Tamary, Hannah, et al.. (1999). NO RESPONSE TO RECOMBINANT HUMAN ERYTHROPOIETIN THERAPY IN PATIENTS WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE I. Pediatric Hematology and Oncology. 16(2). 165–168. 11 indexed citations
18.
Ying, Lihua, Yitzhak Katz, Menachem Schlesinger, et al.. (1999). Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic Syndrome. The American Journal of Human Genetics. 65(6). 1538–1546. 96 indexed citations
19.
Tamary, Hannah, Lea Shalmon, Hanna Shalev, et al.. (1998). Localization of the Gene for Congenital Dyserythropoietic Anemia Type I to a <1-cM Interval on Chromosome 15q15.1-15.3. The American Journal of Human Genetics. 62(5). 1062–1069. 42 indexed citations
20.
Shalev, Hanna, Menachem Schlesinger, Yitzhak Katz, et al.. (1998). Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H. Pediatric Nephrology. 12(8). 619–624. 65 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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