Alexander A.L. Jorge

7.2k total citations
185 papers, 3.8k citations indexed

About

Alexander A.L. Jorge is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Alexander A.L. Jorge has authored 185 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 104 papers in Molecular Biology, 96 papers in Genetics and 78 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Alexander A.L. Jorge's work include Growth Hormone and Insulin-like Growth Factors (68 papers), Genetic Syndromes and Imprinting (25 papers) and Protein Tyrosine Phosphatases (24 papers). Alexander A.L. Jorge is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (68 papers), Genetic Syndromes and Imprinting (25 papers) and Protein Tyrosine Phosphatases (24 papers). Alexander A.L. Jorge collaborates with scholars based in Brazil, United States and Spain. Alexander A.L. Jorge's co-authors include Berenice B. Mendonça, Ivo J.P. Arnhold, Alexsandra C. Malaquias, Mirian Yumie Nishi, Gabriela A. Vasques, Antônio Marcondes Lerário, Ana Cláudia Latronico, Mariana F.A. Funari, Débora Romeo Bertola and Luciani R. Carvalho and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Diabetes.

In The Last Decade

Alexander A.L. Jorge

172 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alexander A.L. Jorge Brazil	36	2.0k	1.7k	1.5k	526	467	185	3.8k
Lawrence S. Mathews United States	28	3.0k 1.5×	1.1k 0.6×	1.9k 1.2×	180 0.3×	417 0.9×	35	4.7k
Peter Wieacker Germany	35	2.4k 1.2×	1.6k 1.0×	255 0.2×	194 0.4×	191 0.4×	141	3.8k
Laurence Legeai‐Mallet France	36	2.7k 1.3×	2.5k 1.5×	241 0.2×	159 0.3×	417 0.9×	87	4.7k
Koji Muroya Japan	28	1.9k 0.9×	1.9k 1.1×	719 0.5×	129 0.2×	377 0.8×	119	3.1k
Bruno Leheup France	29	1.1k 0.5×	758 0.5×	234 0.2×	238 0.5×	239 0.5×	97	2.2k
Monique Losekoot Netherlands	34	1.4k 0.7×	1.3k 0.8×	762 0.5×	82 0.2×	300 0.6×	125	3.1k
Irène Netchine France	34	2.4k 1.2×	2.6k 1.5×	993 0.7×	60 0.1×	327 0.7×	101	3.9k
Yisrael Sidis United States	32	2.1k 1.0×	568 0.3×	292 0.2×	158 0.3×	192 0.4×	47	4.1k
Sarina G. Kant Netherlands	26	1.4k 0.7×	1.3k 0.8×	451 0.3×	523 1.0×	193 0.4×	70	2.7k
Steven Mumm United States	35	2.2k 1.1×	1.2k 0.7×	1.3k 0.8×	136 0.3×	345 0.7×	126	5.2k

Countries citing papers authored by Alexander A.L. Jorge

Since Specialization

Citations

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

Fields of papers citing papers by Alexander A.L. Jorge

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexander A.L. Jorge. 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 Alexander A.L. Jorge. The network helps show where Alexander A.L. Jorge may publish in the future.

Co-authorship network of co-authors of Alexander A.L. Jorge

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

All Works

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20 of 20 papers shown

Ceroni, José Ricardo Magliocco, Guilherme Lopes Yamamoto, Alexander A.L. Jorge, et al.. (2024). Split Hand‐Foot Malformations—Unveiling Unique Molecular Diagnosis From a Brazilian Cohort. Clinical Genetics. 107(4). 453–457.

Dauber, Andrew, et al.. (2024). Clinical Predictors of Good/Poor Response to Growth Hormone Treatment in Children with Idiopathic Short Stature. Hormone Research in Paediatrics. 1–20. 4 indexed citations

Canton, Ana Pinheiro Machado, Luciana Ribeiro Montenegro, Carlos Eduardo Seraphim, et al.. (2023). Clinical and Genetic Characterization of Familial Central Precocious Puberty. The Journal of Clinical Endocrinology & Metabolism. 108(7). 1758–1767. 9 indexed citations

Vasques, Gabriela A., et al.. (2023). Idiopathic Short Stature: What to Expect from Genomic Investigations. SHILAP Revista de lepidopterología. 4(1). 1–17. 6 indexed citations

Funari, Mariana F.A., Antônio Marcondes Lerário, Crésio Alves, et al.. (2023). Identification of a second genetic alteration in patients withSHOXdeficiency individuals: a potential explanation for phenotype variability. European Journal of Endocrinology. 189(3). 387–395. 1 indexed citations

Chong, Karen, David Chitayat, Kelly L. Gilmore, et al.. (2023). Diagnosis of TBC1D32‐associated conditions: Expanding the phenotypic spectrum of a complex ciliopathy. American Journal of Medical Genetics Part A. 191(5). 1282–1292. 1 indexed citations

Montenegro, Luciana Ribeiro, Mirian Yumie Nishi, Alexander A.L. Jorge, et al.. (2022). High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort. Journal of the Endocrine Society. 6(9). bvac106–bvac106. 14 indexed citations

Narcizo, Amanda de Moraes, Anna Benedetti, Alexander A.L. Jorge, et al.. (2022). Targeted massively parallel sequencing panel to diagnose genetic endocrine disorders in a tertiary hospital. Clinics. 77. 100132–100132.

Freire, Bruna Lucheze, et al.. (2019). Growth Hormone insensitivity (Laron syndrome): Report of a new family and review of Brazilian patients. Genetics and Molecular Biology. 42(4). e20180197–e20180197. 6 indexed citations

10.

Reis, André F., Letícia Schwerz Weinert, Sandra Pinho Silveiro, et al.. (2019). Targeted sequencing identifies novel variants in common and rare MODY genes. Molecular Genetics & Genomic Medicine. 7(12). e962–e962. 23 indexed citations

11.

Funari, Mariana F.A., Antônio Marcondes Lerário, Bruna Lucheze Freire, et al.. (2019). Evaluation of SHOX defects in the era of next‐generation sequencing. Clinical Genetics. 96(3). 261–265. 9 indexed citations

12.

Gomes, Larissa Garcia, Marina Cunha-Silva, Carolina Ramos, et al.. (2018). DLK1 Is a Novel Link Between Reproduction and Metabolism. The Journal of Clinical Endocrinology & Metabolism. 104(6). 2112–2120. 91 indexed citations

13.

Canton, Ana Pinheiro Machado, Vinícius Nahime Brito, Luciana Ribeiro Montenegro, et al.. (2018). Clinical and Genetic Features of Central Precocious Puberty Associated with Complex Phenotypes. 1 indexed citations

14.

Imagawa, Eri, Bertrand Isidor, Satomi Mitsuhashi, et al.. (2018). Novel SUZ12 mutations in Weaver‐like syndrome. Clinical Genetics. 94(5). 461–466. 28 indexed citations

15.

Jorge, Alexander A.L., Regina Matsunaga Martin, Luciana Ribeiro Montenegro, et al.. (2016). A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD). European Journal of Endocrinology. 175(2). K7–K15. 2 indexed citations

16.

Trarbach, Ericka Barbosa, Le Min, Alexander A.L. Jorge, et al.. (2014). Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay. Fertility and Sterility. 102(3). 838–846.e2. 32 indexed citations

17.

Pereira, Alexandre C., Chong Ae Kim, Alexsandra C. Malaquias, et al.. (2010). PTPN11 and KRAS Gene Analysis in Patients with Noonan and Noonan-Like Syndromes. Genetic Testing and Molecular Biomarkers. 14(3). 425–432. 26 indexed citations

18.

Jorge, Alexander A.L., et al.. (2002). Poor Reproducibility of IGF-I and IGF Binding Protein-3 Generation Test in Children with Short Stature and Normal Coding Region of the GH Receptor Gene. The Journal of Clinical Endocrinology & Metabolism. 87(2). 469–472. 28 indexed citations

19.

Jorge, Alexander A.L.. (2002). Poor Reproducibility of IGF-I and IGF Binding Protein-3 Generation Test in Children with Short Stature and Normal Coding Region of the GH Receptor Gene. The Journal of Clinical Endocrinology & Metabolism. 87(2). 469–472. 16 indexed citations

20.

Lin, Chin Jia, Alexander A.L. Jorge, Ana Cláudia Latronico, et al.. (2000). Origin of an Ovarian Steroid Cell Tumor Causing Isosexual Pseudoprecocious Puberty Demonstrated by the Expression of Adrenal Steroidogenic Enzymes and Adrenocorticotropin Receptor. The Journal of Clinical Endocrinology & Metabolism. 85(3). 1211–1214. 23 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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