Pamela Trapane

1.9k total citations
16 papers, 247 citations indexed

About

Pamela Trapane is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Pamela Trapane has authored 16 papers receiving a total of 247 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 2 papers in Nephrology. Recurrent topics in Pamela Trapane's work include Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (2 papers) and BRCA gene mutations in cancer (2 papers). Pamela Trapane is often cited by papers focused on Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (2 papers) and BRCA gene mutations in cancer (2 papers). Pamela Trapane collaborates with scholars based in United States, Canada and Australia. Pamela Trapane's co-authors include Paul Coucke, Tammy M. Holm, Marjolijn Renard, Osman Başpınar, Majed Dasouki, Juliane Hoyer, Regan Veith, Bert Callewaert, Bart Loeys and Anita Rauch and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and Genetics in Medicine.

In The Last Decade

Pamela Trapane

13 papers receiving 244 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Pamela Trapane United States	7	131	82	53	39	30	16	247
Ruolan Guo China	11	120 0.9×	158 1.9×	37 0.7×	11 0.3×	14 0.5×	41	332
Magdalena Badura‐Stronka Poland	12	141 1.1×	183 2.2×	22 0.4×	20 0.5×	20 0.7×	32	357
Sonia Nizard France	10	227 1.7×	131 1.6×	16 0.3×	13 0.3×	27 0.9×	12	357
Goran Čuturilo Serbia	11	149 1.1×	167 2.0×	43 0.8×	10 0.3×	7 0.2×	32	323
Marije Meuwissen Belgium	11	186 1.4×	153 1.9×	25 0.5×	49 1.3×	4 0.1×	23	368
Maya Chopra United States	11	174 1.3×	151 1.8×	18 0.3×	7 0.2×	20 0.7×	25	406
Wee Teik Keng Malaysia	11	183 1.4×	183 2.2×	50 0.9×	15 0.4×	58 1.9×	20	420
Gundula Povysil United States	9	141 1.1×	131 1.6×	33 0.6×	15 0.4×	6 0.2×	18	314
Güven Toksoy Türkiye	12	116 0.9×	185 2.3×	15 0.3×	25 0.6×	8 0.3×	51	353
Marylène Rousseau Canada	8	125 1.0×	106 1.3×	26 0.5×	111 2.8×	7 0.2×	9	345

Countries citing papers authored by Pamela Trapane

Since Specialization

Citations

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

Fields of papers citing papers by Pamela Trapane

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pamela Trapane

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

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Rodan, Lance H., Joan M. Stoler, Emily Chen, et al.. (2025). Genetic Evaluation of the Child With Intellectual Disability or Global Developmental Delay: Clinical Report. PEDIATRICS. 156(1). 1 indexed citations

Scheuerle, Angela E., Timothy A. Geleske, Paula Goldenberg, et al.. (2025). Health Supervision for Children With 22q11.2 Deletion Syndrome: Clinical Report. PEDIATRICS. 156(2).

Burnside, Rachel D., et al.. (2025). Reconciling competencies in undergraduate medical genetics education: APHMG versus PCME competencies. Genetics in Medicine. 27(7). 101448–101448.

Priestley, Jessica, Anjali Aggarwal, Cesar Alves, et al.. (2022). Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature. Molecular Genetics and Metabolism Reports. 33. 100931–100931. 10 indexed citations

Trapane, Pamela, et al.. (2022). RF30 | PSAT178 Severe Hyperparathyroidism in a Newborn: Response to Cinacalcet. Journal of the Endocrine Society. 6(Supplement_1). A233–A233.

Shchelochkov, Oleg A., et al.. (2021). Case report of a pseudo‐isodicentric chromosome 9 resulting in mosaic trisomy 9. SHILAP Revista de lepidopterología. 9(4). 2340–2344. 2 indexed citations

Karolak, Justyna A., Albino Bacolla, Qian Liu, et al.. (2019). A recurrent 8 bp frameshifting indel in FOXF1 defines a novel mutation hotspot associated with alveolar capillary dysplasia with misalignment of pulmonary veins. American Journal of Medical Genetics Part A. 179(11). 2272–2276. 3 indexed citations

Harshman, Lyndsay A., Bobby G. Ng, Hudson H. Freeze, et al.. (2016). Congenital nephrotic syndrome in an infant with ALG1‐congenital disorder of glycosylation. Pediatrics International. 58(8). 785–788. 8 indexed citations

Klein-Tasman, Bonnie, et al.. (2014). Relations Between Executive Functioning and Academic Performance in Adolescents with Neurofibromatosis-1. Journal of Developmental and Physical Disabilities. 26(4). 431–450. 6 indexed citations

10.

Klein-Tasman, Bonnie, et al.. (2013). Cognitive and Psychosocial Phenotype of Young Children with Neurofibromatosis-1. Journal of the International Neuropsychological Society. 20(1). 88–98. 35 indexed citations

11.

Quintero, Diana, et al.. (2011). A Rare Presentation of Neonatal Stridor. Clinical Pediatrics. 51(3). 294–296. 2 indexed citations

12.

Renard, Marjolijn, Tammy M. Holm, Regan Veith, et al.. (2010). Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency. European Journal of Human Genetics. 18(8). 895–901. 95 indexed citations

13.

Dimmock, David, Pamela Trapane, Annette Feigenbaum, et al.. (2009). Novel human pathological mutations. Gene symbol: ASS1. Disease: Citrullinaemia.. PubMed. 126(2). 341–341. 2 indexed citations

14.

Dimmock, David, Pamela Trapane, Annette Feigenbaum, et al.. (2008). The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia. American Journal of Medical Genetics Part A. 146A(22). 2885–2890. 24 indexed citations

15.

Reis, Linda M., Rebecca C. Tyler, Omar Abdul‐Rahman, et al.. (2008). Mutation analysis of B3GALTL in Peters Plus syndrome. American Journal of Medical Genetics Part A. 146A(20). 2603–2610. 46 indexed citations

16.

Ghataorhe, Pavandeep, Allison W. Kurian, Pamela Trapane, et al.. (2007). A carrier of both MEN1 and BRCA2 mutations: case report and review of the literature. Cancer Genetics and Cytogenetics. 179(2). 89–92. 13 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