Pedro Louro

418 total citations
11 papers, 112 citations indexed

About

Pedro Louro is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Pedro Louro has authored 11 papers receiving a total of 112 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Pedro Louro's work include Genetics and Neurodevelopmental Disorders (3 papers), Glycosylation and Glycoproteins Research (2 papers) and BRCA gene mutations in cancer (2 papers). Pedro Louro is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Glycosylation and Glycoproteins Research (2 papers) and BRCA gene mutations in cancer (2 papers). Pedro Louro collaborates with scholars based in Portugal, United States and Canada. Pedro Louro's co-authors include Victoria McKay, Daniela T. Pilz, David Fitzpatrick, Arash Hatefi, Anna de Burca, Jill Smith, Alan Fryer, Susan Tomkins, Esther Kinning and Kate Chandler and has published in prestigious journals such as Cancer Research, Journal of Controlled Release and Human Molecular Genetics.

In The Last Decade

Pedro Louro

11 papers receiving 112 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Pedro Louro Portugal	6	66	44	17	15	14	11	112
Arman Çakar Türkiye	8	86 1.3×	20 0.5×	33 1.9×	16 1.1×	11 0.8×	34	193
Siquan Chen United States	9	125 1.9×	20 0.5×	21 1.2×	22 1.5×	9 0.6×	14	190
G. C. Chan United Kingdom	2	87 1.3×	129 2.9×	10 0.6×	6 0.4×	6 0.4×	3	193
Mary Koziura United States	4	51 0.8×	70 1.6×	13 0.8×	8 0.5×	7 0.5×	5	114
Kirsi Alakurtti Finland	7	88 1.3×	129 2.9×	12 0.7×	6 0.4×	6 0.4×	9	233
Céline Poirsier France	5	64 1.0×	29 0.7×	14 0.8×	27 1.8×	13 0.9×	6	125
Erica L. Macke United States	7	76 1.2×	18 0.4×	8 0.5×	5 0.3×	8 0.6×	16	122
Benjamin Kamien Australia	9	124 1.9×	128 2.9×	12 0.7×	6 0.4×	4 0.3×	19	228
Newell Belnap United States	7	84 1.3×	49 1.1×	7 0.4×	3 0.2×	5 0.4×	12	126
Girolamo Aurelio Vitello Italy	6	43 0.7×	25 0.6×	19 1.1×	3 0.2×	9 0.6×	17	96

Countries citing papers authored by Pedro Louro

Since Specialization

Citations

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

Fields of papers citing papers by Pedro Louro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pedro Louro

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

All Works

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11 of 11 papers shown

Vandavasi, Venu Gopal, Ge Yang, Pedro Louro, et al.. (2023). A high affinity and specificity anti-HER2 single-domain antibody (VHH) that targets trastuzumab’s epitope with versatile biochemical, biological, and medical applications. Immunologic Research. 72(1). 103–118. 7 indexed citations

Awamleh, Zain, Sanaa Choufani, Cheryl Cytrynbaum, et al.. (2022). ANKRD11 pathogenic variants and 16q24.3 microdeletions share an altered DNA methylation signature in patients with KBG syndrome. Human Molecular Genetics. 32(9). 1429–1438. 7 indexed citations

Valero-Ramón, Zoe, Pedro Louro, Nikolaos Papachristou, et al.. (2022). A Collective Intelligence Platform to Support Older Cancer Survivors: Towards the Definition of LifeChamps System and Big Data Reference Architecture. Studies in health technology and informatics. 290. 1008–1009. 2 indexed citations

Matos, Leonor Vasconcelos de, et al.. (2021). Challenges and Considerations on Risk-Reducing Surgery in BRCA1/2 Patients with Advanced Breast Cancer. Current Oncology. 28(1). 485–490. 2 indexed citations

Rodrigues, Paula, et al.. (2020). Abstract P6-08-17: When BRCA2-breast cancer is more prevalent than BRCA1-breast cancer: Prospective follow-up data from a multidisciplinary program. Cancer Research. 80(4_Supplement). P6–8. 2 indexed citations

Sarkar, Siddik, Alireza Nomani, Michael Goedken, et al.. (2019). Bioengineered adipose-derived stem cells for targeted enzyme-prodrug therapy of ovarian cancer intraperitoneal metastasis. Journal of Controlled Release. 311-312. 273–287. 18 indexed citations

Louro, Pedro, et al.. (2019). Woodhouse–Sakati Syndrome: First report of a Portuguese case. American Journal of Medical Genetics Part A. 179(11). 2237–2240. 9 indexed citations

Dupuis, Lucie, et al.. (2019). 16q22.1 microdeletion and anticipatory guidance. American Journal of Medical Genetics Part A. 179(7). 1287–1292. 1 indexed citations

Merolli, Antonio, Pedro Louro, & Joachim Kohn. (2018). Reciprocal nerve staining (RNS) for the concurrent detection of choline acetyltransferase and myelin basic protein on paraffin-embedded sections. Journal of Neuroscience Methods. 311. 235–238. 3 indexed citations

10.

Kharbanda, Mira, Daniela T. Pilz, Susan Tomkins, et al.. (2016). Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals. European Journal of Medical Genetics. 60(2). 130–135. 46 indexed citations

11.

Louro, Pedro, Lina Ramos, Alexandra Dinis, et al.. (2016). Phenotyping GABA transaminase deficiency: a case description and literature review. Journal of Inherited Metabolic Disease. 39(5). 743–747. 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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