Liat Ganon

736 total citations
14 papers, 513 citations indexed

About

Liat Ganon is a scholar working on Nephrology, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, Liat Ganon has authored 14 papers receiving a total of 513 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Nephrology, 8 papers in Pathology and Forensic Medicine and 3 papers in Molecular Biology. Recurrent topics in Liat Ganon's work include Vitamin D Research Studies (4 papers), Parathyroid Disorders and Treatments (4 papers) and Gout, Hyperuricemia, Uric Acid (4 papers). Liat Ganon is often cited by papers focused on Vitamin D Research Studies (4 papers), Parathyroid Disorders and Treatments (4 papers) and Gout, Hyperuricemia, Uric Acid (4 papers). Liat Ganon collaborates with scholars based in Israel, United States and United Kingdom. Liat Ganon's co-authors include Dganit Dinour, Eli J. Holtzman, Eliezer J. Holtzman, Ben-Ami Sela, Zemach Eisenstein, Alan F. Wright, Karen Tordjman, Xinhua Shu, Nicola K. Gray and Lindsay Sawyer and has published in prestigious journals such as Journal of the American Society of Nephrology, The Journal of Urology and Nephrology Dialysis Transplantation.

In The Last Decade

Liat Ganon

14 papers receiving 503 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Liat Ganon Israel	9	318	291	149	102	97	14	513
Jürgen Floege Germany	5	441 1.4×	132 0.5×	52 0.3×	107 1.0×	51 0.5×	8	559
Jorge Rojas-Rivera Spain	14	408 1.3×	208 0.7×	88 0.6×	57 0.6×	70 0.7×	29	602
Miho Hikita Japan	8	539 1.7×	240 0.8×	173 1.2×	193 1.9×	32 0.3×	23	661
Robert Dunlay United States	10	264 0.8×	65 0.2×	121 0.8×	75 0.7×	62 0.6×	12	480
Anca Gal‐Moscovici Israel	11	247 0.8×	101 0.3×	41 0.3×	37 0.4×	33 0.3×	21	370
Lillian Yau United States	6	215 0.7×	127 0.4×	85 0.6×	62 0.6×	58 0.6×	7	391
Hun Sub Shin South Korea	6	274 0.9×	171 0.6×	90 0.6×	47 0.5×	118 1.2×	15	468
Claudia Fofi Italy	9	209 0.7×	36 0.1×	98 0.7×	61 0.6×	46 0.5×	21	447
Robert C. Kopelman United States	9	308 1.0×	91 0.3×	78 0.5×	39 0.4×	46 0.5×	12	633
Tatjana Damjanović Serbia	11	252 0.8×	40 0.1×	100 0.7×	105 1.0×	38 0.4×	28	572

Countries citing papers authored by Liat Ganon

Since Specialization

Citations

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

Fields of papers citing papers by Liat Ganon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Liat Ganon

This figure shows the co-authorship network connecting the top 25 collaborators of Liat Ganon. A scholar is included among the top collaborators of Liat Ganon 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 Liat Ganon. Liat Ganon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Ganon, Liat, et al.. (2021). Childhood Hypercalciuric Hypercalcemia With Elevated Vitamin D and Suppressed Parathyroid Hormone: Long-Term Follow Up. Frontiers in Pediatrics. 9. 752312–752312. 7 indexed citations

Kunin, Margarita, Liat Ganon, Eli J. Holtzman, & Dganit Dinour. (2018). Hyponatremia in refractory congestive heart failure patients treated with icodextrin-based peritoneal dialysis: A case series. Nefrología (English Edition). 38(1). 87–91. 1 indexed citations

Hanukoglu, Aaron, et al.. (2017). Familial Hyperkalemia and Hypertension (FHHt) and KLHL3: Description of a Family with a New Recessive Mutation (S553L) Compared to a Family with a Dominant Mutation, Q309R, with Analysis of Urinary Sodium Chloride Cotransporter. The Nephron journals/Nephron journals. 137(1). 77–84. 9 indexed citations

Kunin, Margarita, Liat Ganon, Eli J. Holtzman, & Dganit Dinour. (2017). Hyponatremia in refractory congestive heart failure patients treated with icodextrin-based peritoneal dialysis: A case series. Nefrología. 38(1). 87–91. 3 indexed citations

Dinour, Dganit, Miriam Davidovits, Liat Ganon, et al.. (2016). Loss of function of NaPiIIa causes nephrocalcinosis and possibly kidney insufficiency. Pediatric Nephrology. 31(12). 2289–2297. 29 indexed citations

Dinour, Dganit, et al.. (2014). Wild-type uromodulin prevents NFkB activation in kidney cells, while mutant uromodulin, causing FJHU nephropathy, does not. Journal of Nephrology. 27(3). 257–264. 5 indexed citations

Dinour, Dganit, Miriam Davidovits, Shraga Aviner, et al.. (2014). Maternal and infantile hypercalcemia caused by vitamin-D-hydroxylase mutations and vitamin D intake. Pediatric Nephrology. 30(1). 145–152. 55 indexed citations

Colussi, Giacomo, Liat Ganon, Silvana Penco, et al.. (2013). Chronic hypercalcaemia from inactivating mutations of vitamin D 24-hydroxylase (CYP24A1): implications for mineral metabolism changes in chronic renal failure. Nephrology Dialysis Transplantation. 29(3). 636–643. 43 indexed citations

Dinour, Dganit, Pazit Beckerman, Liat Ganon, et al.. (2013). Loss-of-Function Mutations of CYP24A1 , the Vitamin D 24-Hydroxylase Gene, Cause Long-standing Hypercalciuric Nephrolithiasis and Nephrocalcinosis. The Journal of Urology. 190(2). 552–557. 84 indexed citations

10.

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

11.

Dinour, Dganit, Andrew Bahn, Liat Ganon, et al.. (2010). URAT1 mutations cause renal hypouricemia type 1 in Iraqi Jews. Nephrology Dialysis Transplantation. 26(7). 2175–2181. 47 indexed citations

12.

Dinour, Dganit, et al.. (2010). Molecular Study of Proteinuria in Patients Treated with B<sub>12</sub> Supplements: Do Not Forget Megaloblastic Anemia Type 1. Nephron Clinical Practice. 118(2). c67–c71. 6 indexed citations

13.

Dinour, Dganit, Nicola K. Gray, Susan Campbell, et al.. (2009). Homozygous SLC2A9 Mutations Cause Severe Renal Hypouricemia. Journal of the American Society of Nephrology. 21(1). 64–72. 174 indexed citations

14.

Bahat, Hilla Sarig, Dganit Dinour, Liat Ganon, et al.. (2009). Non-urate transporter 1-related renal hypouricemia and acute renal failure in an Israeli–Arab family. Pediatric Nephrology. 24(5). 999–1003. 8 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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