Juan Bernar

550 total citations
14 papers, 354 citations indexed

About

Juan Bernar is a scholar working on Molecular Biology, Biochemistry and Pathology and Forensic Medicine. According to data from OpenAlex, Juan Bernar has authored 14 papers receiving a total of 354 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Biochemistry and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Juan Bernar's work include Amino Acid Enzymes and Metabolism (6 papers), Biomedical Research and Pathophysiology (5 papers) and Neonatal Health and Biochemistry (4 papers). Juan Bernar is often cited by papers focused on Amino Acid Enzymes and Metabolism (6 papers), Biomedical Research and Pathophysiology (5 papers) and Neonatal Health and Biochemistry (4 papers). Juan Bernar collaborates with scholars based in United States, Spain and Tunisia. Juan Bernar's co-authors include William A. Gahl, Isa Bernardini, Marinos C. Dalakas, William B. Rizzo, G. S. Harper, Leonard D. Kohn, Frank Tietze, Evelyn F. Grollman, R S Sparkes and Michael H. Fox and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and The Journal of Pediatrics.

In The Last Decade

Juan Bernar

14 papers receiving 337 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Juan Bernar United States	11	130	114	110	109	98	14	354
Miguel Angel Alcántara‐Ortigoza Mexico	12	78 0.6×	163 1.4×	32 0.3×	45 0.4×	26 0.3×	57	386
S Scheibenreiter Austria	10	135 1.0×	176 1.5×	11 0.1×	267 2.4×	94 1.0×	35	416
Zhiyong Chen Switzerland	5	46 0.4×	91 0.8×	65 0.6×	50 0.5×	50 0.5×	7	230
Fatma Al‐Jasmi United Arab Emirates	10	35 0.3×	103 0.9×	24 0.2×	67 0.6×	14 0.1×	20	280
Ekaterina Tsilou United States	6	40 0.3×	106 0.9×	40 0.4×	118 1.1×	77 0.8×	6	246
Serap Sivri Türkiye	11	52 0.4×	120 1.1×	16 0.1×	182 1.7×	46 0.5×	53	342
A. Green United Kingdom	11	81 0.6×	179 1.6×	11 0.1×	305 2.8×	120 1.2×	28	415
Boris Gebhardt Germany	10	72 0.6×	219 1.9×	11 0.1×	176 1.6×	36 0.4×	12	422
Ee Shien Tan Singapore	12	44 0.3×	158 1.4×	11 0.1×	121 1.1×	35 0.4×	27	351
W. R. Bergren United States	9	120 0.9×	81 0.7×	11 0.1×	167 1.5×	64 0.7×	15	313

Countries citing papers authored by Juan Bernar

Since Specialization

Citations

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

Fields of papers citing papers by Juan Bernar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Juan Bernar

This figure shows the co-authorship network connecting the top 25 collaborators of Juan Bernar. A scholar is included among the top collaborators of Juan Bernar 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 Juan Bernar. Juan Bernar 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

Parry, David, Mihail Halachev, Kathleen A. Williamson, et al.. (2023). Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia. Journal of Medical Genetics. 61(3). 250–261. 4 indexed citations

Bernar, Juan, et al.. (2021). Squamous cell carcinoma arising from an epidermal inclusion cyst in breast: An extremely rare diagnosis. The Breast Journal. 27(2). 176–177. 1 indexed citations

Gago‐Veiga, Ana Beatriz, et al.. (2018). Specificity of electroclinical features in the diagnosis of ring chromosome 20. Epilepsy & Behavior. 80. 215–220. 10 indexed citations

Pérez‐Cerdá, Celia, B. Merinero, María Jesús García García, et al.. (2002). Screening for Adenylosuccinate Lyase Deficiency: Clinical, Biochemical and Molecular Findings in Four Patients. Neuropediatrics. 33(4). 186–189. 22 indexed citations

Gahl, William A., Isa Bernardini, Marinos C. Dalakas, et al.. (1988). Oral carnitine therapy in children with cystinosis and renal Fanconi syndrome.. Journal of Clinical Investigation. 81(2). 549–560. 33 indexed citations

Charnas, Lawrence, Juan Bernar, G. Pezeshkpour, et al.. (1988). MRI Findings and Peripheral Neuropathy in Lowe's Syndrome. Neuropediatrics. 19(1). 7–9. 23 indexed citations

Harper, G. S., Leonard D. Kohn, Isa Bernardini, et al.. (1988). Thyrotropin stimulation of lysosomal tyrosine transport in rat FRTL-5 thyroid cells.. Journal of Biological Chemistry. 263(19). 9320–9325. 11 indexed citations

Lin, Angela E., Juan Bernar, Alvin J. Chin, et al.. (1986). Congenital heart disease in supernumerary der(22), t(11;22) syndrome. Clinical Genetics. 29(4). 269–275. 32 indexed citations

Bernar, Juan, et al.. (1986). Arginase deficiency in a 12-year-old boy with mild impairment of intellectual function. The Journal of Pediatrics. 108(3). 432–435. 27 indexed citations

10.

Bernar, Juan, Frank Tietze, Leonard D. Kohn, et al.. (1986). Characteristics of a lysosomal membrane transport system for tyrosine and other neutral amino acids in rat thyroid cells.. Journal of Biological Chemistry. 261(36). 17107–17112. 53 indexed citations

11.

Bass, Harold N., et al.. (1985). A family with three independent autosomal translocations associated with 7q32----7qter syndrome.. Journal of Medical Genetics. 22(1). 59–63. 34 indexed citations

12.

Bernardini, Isa, William B. Rizzo, Marinos C. Dalakas, Juan Bernar, & William A. Gahl. (1985). Plasma and muscle free carnitine deficiency due to renal Fanconi syndrome.. Journal of Clinical Investigation. 75(4). 1124–1130. 88 indexed citations

13.

Bernar, Juan, et al.. (1985). 1196 PLASMA AND MUSCLE CARNITINE DEFICIENCY IN RENAL FANCONI SYNDROME. Pediatric Research. 19(4). 310A–310A. 1 indexed citations

14.

Bernar, Juan, et al.. (1985). Interstitial deletion 2q24.3: case report with high resolution banding.. Journal of Medical Genetics. 22(3). 226–228. 15 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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