Abdulsalam Abu‐Libdeh

582 total citations
25 papers, 338 citations indexed

About

Abdulsalam Abu‐Libdeh is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Abdulsalam Abu‐Libdeh has authored 25 papers receiving a total of 338 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Surgery. Recurrent topics in Abdulsalam Abu‐Libdeh's work include Sexual Differentiation and Disorders (3 papers), Ion Transport and Channel Regulation (3 papers) and Regulation of Appetite and Obesity (3 papers). Abdulsalam Abu‐Libdeh is often cited by papers focused on Sexual Differentiation and Disorders (3 papers), Ion Transport and Channel Regulation (3 papers) and Regulation of Appetite and Obesity (3 papers). Abdulsalam Abu‐Libdeh collaborates with scholars based in Israel, United States and Palestinian Territory. Abdulsalam Abu‐Libdeh's co-authors include David Zangen, Ephrat Levy‐Lahad, Paul Renbaum, Moien Kanaan, Sharon Zeligson, Liran Carmel, Yotam Kaufman, Ariella Weinberg‐Shukron, Avital Perry and Ayal B. Gussow and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Clinical Endocrinology & Metabolism and Diabetes.

In The Last Decade

Abdulsalam Abu‐Libdeh

21 papers receiving 334 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Abdulsalam Abu‐Libdeh Israel 10 187 115 75 66 53 25 338
Vickie Hannig United States 12 175 0.9× 185 1.6× 70 0.9× 34 0.5× 36 0.7× 19 494
Yoon-Myung Kim South Korea 12 117 0.6× 60 0.5× 37 0.5× 30 0.5× 41 0.8× 34 351
N. E. Skakkeb�k Denmark 11 166 0.9× 115 1.0× 79 1.1× 108 1.6× 34 0.6× 13 404
Javier Aisenberg United States 11 155 0.8× 91 0.8× 188 2.5× 43 0.7× 48 0.9× 18 400
Massimo Realacci Italy 11 57 0.3× 66 0.6× 69 0.9× 80 1.2× 26 0.5× 17 321
Pilar Andaluz Spain 14 266 1.4× 249 2.2× 273 3.6× 39 0.6× 38 0.7× 20 539
Ayako Ito Japan 10 105 0.6× 27 0.2× 77 1.0× 68 1.0× 51 1.0× 27 322
Masashi Kitagawa Japan 8 104 0.6× 39 0.3× 49 0.7× 47 0.7× 48 0.9× 21 234
Zehra Yavaş Abalı Türkiye 9 147 0.8× 82 0.7× 100 1.3× 26 0.4× 13 0.2× 48 243
Eef Hoeben Belgium 14 138 0.7× 65 0.6× 70 0.9× 86 1.3× 55 1.0× 22 394

Countries citing papers authored by Abdulsalam Abu‐Libdeh

Since Specialization
Citations

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

Fields of papers citing papers by Abdulsalam Abu‐Libdeh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Abdulsalam Abu‐Libdeh. 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 Abdulsalam Abu‐Libdeh. The network helps show where Abdulsalam Abu‐Libdeh may publish in the future.

Co-authorship network of co-authors of Abdulsalam Abu‐Libdeh

This figure shows the co-authorship network connecting the top 25 collaborators of Abdulsalam Abu‐Libdeh. A scholar is included among the top collaborators of Abdulsalam Abu‐Libdeh 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 Abdulsalam Abu‐Libdeh. Abdulsalam Abu‐Libdeh 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.
Nazemi, Haleh, et al.. (2024). Micromachined Capacitive Sensor With Configured Boundaries: Approach, Design and Fabrication. IEEE Transactions on Electron Devices. 71(12). 7758–7764.
2.
Rossetti, Raffaella, Abraham O. Samson, Paul Renbaum, et al.. (2024). A Novel Homozygous BMP15 Mutation Causes Ovarian Dysgenesis and Primary Amenorrhea. Journal of the Endocrine Society. 9(2). bvae221–bvae221.
3.
Abu‐Libdeh, Abdulsalam, et al.. (2023). Growth hormone therapy for children with Duchenne muscular dystrophy and glucocorticoid induced short stature. Growth Hormone & IGF Research. 72-73. 101558–101558. 5 indexed citations
4.
Abu‐Libdeh, Abdulsalam, et al.. (2023). Wolfram Syndrome‐2, a Cause of Severe Gastrointestinal Bleeding: A Case Series and a Literature Review. JPGN Reports. 4(3). e339–e339. 1 indexed citations
5.
Zangen, David, et al.. (2022). PMON193 Reactive oxygen species in the development of gonadal failure in late-onset transaldolase deficiency. Journal of the Endocrine Society. 6(Supplement_1). A621–A622. 1 indexed citations
6.
Thacker, Naveen, Enver Hasanoğlu, Leyla S. Namazova-Baranova, et al.. (2021). Global Emergencies in Child Health: Challenges and Solutions—Viewpoint and Recommendations from the European Paediatric Association and the International Pediatric Association. The Journal of Pediatrics. 241. 266–266.e3. 4 indexed citations
7.
Hershkovitz, Eli, Bassam Abu‐Libdeh, Raz Zarivach, et al.. (2021). Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneity. American Journal of Medical Genetics Part A. 185(4). 1033–1038. 1 indexed citations
8.
Levy‐Khademi, Floris, Sharon Zeligson, Boris Chertin, et al.. (2020). The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD. Endocrine. 69(3). 650–654. 2 indexed citations
9.
Shlomai, Noa Ofek, Ariella Weinberg‐Shukron, Süleyman Gülsüner, et al.. (2020). NKX2-2 Mutation Causes Congenital Diabetes and Infantile Obesity With Paradoxical Glucose-Induced Ghrelin Secretion. The Journal of Clinical Endocrinology & Metabolism. 105(11). 3486–3495. 11 indexed citations
10.
Abu‐Libdeh, Abdulsalam & Bassam Abu‐Libdeh. (2019). Homozygosity for Proopiomelanocortin (POMC) Mutation in a Palestininan Child. 1 indexed citations
11.
Abu‐Libdeh, Bassam, et al.. (2018). Growth Hormone Deficiency in Congenital Toxoplasmosis. 8(1). e43–e45.
12.
Abu‐Libdeh, Abdulsalam, et al.. (2017). Neonatal Hypopituitarism: Unusual Presentation. 7(1). e103–e105. 2 indexed citations
13.
Weinberg‐Shukron, Ariella, Abdulsalam Abu‐Libdeh, Liran Carmel, et al.. (2015). Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress. Journal of Medical Genetics. 52(9). 636–641. 28 indexed citations
14.
Tenenbaum, Ariel, et al.. (2012). Euthyroid Submedian Free T4 and Subclinical Hypothyroidism May Have a Detrimental Clinical Effect in Down Syndrome. Hormone Research in Paediatrics. 78(2). 113–118. 9 indexed citations
15.
Zangen, David, Yotam Kaufman, Sharon Zeligson, et al.. (2011). XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription. The American Journal of Human Genetics. 89(4). 572–579. 78 indexed citations
16.
Vivante, Asaf, Danny Lotan, Naomi Pode‐Shakked, et al.. (2011). Familial Autosomal Recessive Renal Tubular Acidosis: Importance of Early Diagnosis. Nephron Physiology. 119(3). p31–p39. 8 indexed citations
17.
Abu‐Libdeh, Abdulsalam, et al.. (2010). Propionic acidemia mimicking diabetic ketoacidosis. Brain and Development. 33(5). 428–431. 15 indexed citations
18.
Wexler, Isaiah D., et al.. (2009). Optimizing health care for individuals with Down syndrome in Israel.. PubMed. 11(11). 655–9. 15 indexed citations
19.
Abu‐Libdeh, Abdulsalam, et al.. (2009). Autosomal recessive familial neurohypophyseal diabetes insipidus: onset in early infancy. European Journal of Endocrinology. 162(2). 221–226. 28 indexed citations
20.
Bushman, Jeremy D., Avital Perry, Abdulsalam Abu‐Libdeh, et al.. (2008). Novel De Novo Mutation in Sulfonylurea Receptor 1 Presenting as Hyperinsulinism in Infancy Followed by Overt Diabetes in Early Adolescence. Diabetes. 57(7). 1935–1940. 46 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Vickie Hannig Breakdown of academic impact, for papers by Yoon-Myung Kim Breakdown of academic impact, for papers by N. E. Skakkeb�k Breakdown of academic impact, for papers by Javier Aisenberg Breakdown of academic impact, for papers by Massimo Realacci Breakdown of academic impact, for papers by Pilar Andaluz Breakdown of academic impact, for papers by Ayako Ito Breakdown of academic impact, for papers by Masashi Kitagawa Breakdown of academic impact, for papers by Zehra Yavaş Abalı Breakdown of academic impact, for papers by Eef Hoeben
Rankless by CCL
2026