Hélio Pedro

1.2k total citations
14 papers, 183 citations indexed

About

Hélio Pedro is a scholar working on Physiology, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hélio Pedro has authored 14 papers receiving a total of 183 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Physiology, 4 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hélio Pedro's work include Lysosomal Storage Disorders Research (4 papers), Neonatal Health and Biochemistry (2 papers) and Metabolism and Genetic Disorders (2 papers). Hélio Pedro is often cited by papers focused on Lysosomal Storage Disorders Research (4 papers), Neonatal Health and Biochemistry (2 papers) and Metabolism and Genetic Disorders (2 papers). Hélio Pedro collaborates with scholars based in United States, Canada and United Kingdom. Hélio Pedro's co-authors include Joseph J. Apuzzio, Thorsten Hornemann, Carsten G. Bönnemann, Can Fıçıcıoğlu, Beth A. Pletcher, Jesús Román Martínez Álvarez, Stephen J. Thompson, Eric A. Shoubridge, Robert Wallerstein and Hana Aviv and has published in prestigious journals such as Journal of Clinical Investigation, The American Journal of Gastroenterology and Obstetrics and Gynecology.

In The Last Decade

Hélio Pedro

10 papers receiving 165 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hélio Pedro United States	8	72	57	56	50	33	14	183
Danijela Petković Ramadža Croatia	9	134 1.9×	34 0.6×	49 0.9×	103 2.1×	11 0.3×	26	280
Juan Francisco Cabello Chile	11	86 1.2×	41 0.7×	30 0.5×	126 2.5×	26 0.8×	32	287
Ramona Salvarinova Canada	8	109 1.5×	20 0.4×	40 0.7×	46 0.9×	13 0.4×	18	202
Jaina Patel Canada	8	118 1.6×	42 0.7×	193 3.4×	43 0.9×	34 1.0×	17	389
Kairit Joost Estonia	9	85 1.2×	33 0.6×	31 0.6×	40 0.8×	6 0.2×	17	184
Elisenda Cortès‐Saladelafont Spain	9	99 1.4×	28 0.5×	47 0.8×	47 0.9×	3 0.1×	21	231
Ken Momosaki Japan	10	102 1.4×	45 0.8×	63 1.1×	163 3.3×	45 1.4×	22	286
Miriam Kolníková Slovakia	9	105 1.5×	24 0.4×	40 0.7×	102 2.0×	24 0.7×	26	239
Chaitanya Datar India	6	44 0.6×	31 0.5×	22 0.4×	90 1.8×	19 0.6×	18	130
Xiaoning Bi China	4	87 1.2×	61 1.1×	13 0.2×	160 3.2×	31 0.9×	5	289

Countries citing papers authored by Hélio Pedro

Since Specialization

Citations

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

Fields of papers citing papers by Hélio Pedro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hélio Pedro

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

Schmidt, Sarah, Hélio Pedro, Reena Jethva, et al.. (2025). Newborn Screening for Gaucher Disease: The New Jersey Experience. International Journal of Neonatal Screening. 11(2). 34–34.

Lone, Museer A., Mari J. Aaltonen, Hélio Pedro, et al.. (2022). SPTLC1 variants associated with ALS produce distinct sphingolipid signatures through impaired interaction with ORMDL proteins. Journal of Clinical Investigation. 132(18). 25 indexed citations

Weinreb, Neal J., Özlem Göker-Alpan, Priya S. Kishnani, et al.. (2022). The diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?. Molecular Genetics and Metabolism. 136(1). 4–21. 33 indexed citations

Strong, Alanna, Anthony D. Krentz, Deborah Watson, et al.. (2021). Expanding the genetic landscape of oral‐facial‐digital syndrome with two novel genes. American Journal of Medical Genetics Part A. 185(8). 2409–2416. 11 indexed citations

Pedro, Hélio, et al.. (2020). The IGSF1 Deficiency Syndrome May Present with Normal Free T4 Levels, Severe Obesity, or Premature Testicular Growth. Journal of Clinical Research in Pediatric Endocrinology. 13(4). 461–467. 1 indexed citations

Cohen, Jennifer L., et al.. (2019). Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy. Orphanet Journal of Rare Diseases. 14(1). 198–198. 7 indexed citations

Pedro, Hélio, et al.. (2019). A Case of Reversible Infantile Respiratory Chain Deficiency Presenting With Hypotonia, Hyperammonemia, and Failure to Thrive. Pediatric and Developmental Pathology. 22(6). 590–593.

Rudnick, Sean, Hélio Pedro, John J. Ko, et al.. (2018). The Patient Odyssey to Confirmed Acute Hepatic Porphyria Diagnosis: Clinical Characteristics and Healthcare Utilization of Patients Preceding Diagnosis of Acute Hepatic Porphyria. The American Journal of Gastroenterology. 113(Supplement). S500–S501. 1 indexed citations

Segal, Eric, et al.. (2016). Diagnostic Yield of Epilepsy Panels in Children With Medication-Refractory Epilepsy. Pediatric Neurology. 64. 66–71. 21 indexed citations

10.

Aisenberg, Javier, et al.. (2010). Atypical GH Insensitivity Syndrome and Severe Insulin-Like Growth Factor-I Deficiency Resulting from Compound Heterozygous Mutations of the GH Receptor, Including a Novel Frameshift Mutation Affecting the Intracellular Domain. Hormone Research in Paediatrics. 74(6). 406–411. 13 indexed citations

11.

Pedro, Hélio, Luísa Barros, & Carla Moleiro. (2009). Brief Report: Parents and Nurses' Behaviors Associated with Child Distress during Routine Immunization in a Portuguese Population. Journal of Pediatric Psychology. 35(6). 602–610. 7 indexed citations

12.

Williams, Shauna, Jesús Román Martínez Álvarez, Hélio Pedro, & Joseph J. Apuzzio. (2008). Glutaric Aciduria Type II and Narcolepsy in Pregnancy. Obstetrics and Gynecology. 111(2). 522–524. 13 indexed citations

13.

Wolf, Barry, Kevin P. Jensen, Bruce A. Barshop, et al.. (2005). Biotinidase deficiency: Novel mutations and their biochemical and clinical correlates. Human Mutation. 25(4). 413–413. 30 indexed citations

14.

Wallerstein, Robert, et al.. (2005). Long term follow‐up of developmental delay in a child with prenatally‐diagnosed trisomy 20 mosaicism. American Journal of Medical Genetics Part A. 137A(1). 94–97. 21 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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