Edna E. Mancilla

1.9k total citations · 1 hit paper
29 papers, 1.3k citations indexed

About

Edna E. Mancilla is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Edna E. Mancilla has authored 29 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Pulmonary and Respiratory Medicine and 11 papers in Molecular Biology. Recurrent topics in Edna E. Mancilla's work include Parathyroid Disorders and Treatments (7 papers), Genetic Syndromes and Imprinting (5 papers) and Congenital Heart Disease Studies (5 papers). Edna E. Mancilla is often cited by papers focused on Parathyroid Disorders and Treatments (7 papers), Genetic Syndromes and Imprinting (5 papers) and Congenital Heart Disease Studies (5 papers). Edna E. Mancilla collaborates with scholars based in United States, Chile and Sweden. Edna E. Mancilla's co-authors include Jeffrey Baron, Monique H. A. Kester, Edith C. H. Friesema, Theo J. Visser, Francesco De Luca, Johan Svensson, Maarten Reeser, Timothy Barrett, Patrice Rodien and Sahila Balkassmi and has published in prestigious journals such as The Lancet, Circulation and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Edna E. Mancilla

27 papers receiving 1.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation

2004 512 citations Edith C. H. Friesema, Annette Grueters et al. The Lancet profile →

Peers

Edna E. Mancilla

EDM

GENET

SURGE

NEPHR

Anatoly Tiulpakov Russia

Hans‐Peter Guler Switzerland

Yardena Tenenbaum‐Rakover Israel

Manuel C. Lemos Portugal

Marcello Filopanti Italy

Caroline M. Gorvin United Kingdom

Hakan R. Toka United States

Sebastiano Grasso Italy

Marcel Blot‐Chabaud France

Rita van Bree Belgium

Anatoly Tiulpakov Russia

Edna E. Mancilla

790 ×1.2

EDM

637 ×1.4

454 ×1.1

GENET

229 ×1.6

SURGE

99 ×0.7

NEPHR

Citations per year, relative to Edna E. Mancilla Edna E. Mancilla (= 1×) peers Anatoly Tiulpakov

Countries citing papers authored by Edna E. Mancilla

Since Specialization

Citations

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

Fields of papers citing papers by Edna E. Mancilla

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edna E. Mancilla. 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 Edna E. Mancilla. The network helps show where Edna E. Mancilla may publish in the future.

Co-authorship network of co-authors of Edna E. Mancilla

This figure shows the co-authorship network connecting the top 25 collaborators of Edna E. Mancilla. A scholar is included among the top collaborators of Edna E. Mancilla 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 Edna E. Mancilla. Edna E. Mancilla 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

Simmons, Jill H., Edna E. Mancilla, Steven Mumm, et al.. (2025). Duplications within exon 1 of TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK) are associated with tendon avulsion. Bone. 197. 117486–117486.

Vajravelu, Mary Ellen, Karuna Shekdar, Michael A. Levine, et al.. (2023). Early identification of a 12-bp tandem duplication in TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK): Clinical characterization and response to bisphosphonate therapy. Bone. 170. 116698–116698. 2 indexed citations

Rychik, Jack, David Goldberg, Elizabeth B. Rand, et al.. (2022). A Path FORWARD: Development of a Comprehensive Multidisciplinary Clinic to Create Health and Wellness for the Child and Adolescent with a Fontan Circulation. Pediatric Cardiology. 43(6). 1175–1192. 10 indexed citations

Pignolo, Robert J., Edward C. Hsiao, Mona Al Mukaddam, et al.. (2022). Reduction of New Heterotopic Ossification ( HO ) in the Open‐Label , Phase 3 MOVE Trial of Palovarotene for Fibrodysplasia Ossificans Progressiva ( FOP ). Journal of Bone and Mineral Research. 38(3). 381–394. 32 indexed citations

Mancilla, Edna E., Jeffrey D. Roizen, Kathryn Dodds, et al.. (2021). Growth in Children with a Fontan Circulation. The Journal of Pediatrics. 235. 149–155.e2. 8 indexed citations

Kaplan, Frederick S., David T. Teachey, Jeffrey R. Andolina, et al.. (2021). Off-on-off-on use of imatinib in three children with fibrodysplasia ossificans progressiva. Bone. 150. 116016–116016. 9 indexed citations

Mancilla, Edna E., Jill L. Brodsky, Jeffrey D. Roizen, et al.. (2016). Abstract 19714: Growth Parameters, Bone Mineral Density and Secondary Hyperparathyroidism After Fontan Operation: Results From the Multidisciplinary Clinic at the CHOP Single Ventricle Survivorship Program. Circulation. 134. 1 indexed citations

Mancilla, Edna E., Jill L. Brodsky, Samir Mehta, Robert J. Pignolo, & Michael A. Levine. (2014). Teriparatide as a Systemic Treatment for Lower Extremity Nonunion Fractures: A Case Series. Endocrine Practice. 21(2). 136–142. 22 indexed citations

Goldberg, David, Andrew C. Glatz, Jill L. Brodsky, et al.. (2012). Children With Protein-Losing Enteropathy After the Fontan Operation Are at Risk for Abnormal Bone Mineral Density. Pediatric Cardiology. 33(8). 1264–1268. 24 indexed citations

10.

Varela, Nelson, Marcia Gaete, Julio C. Tapia, et al.. (2009). Impaired cell cycle regulation of the osteoblast‐related heterodimeric transcription factor Runx2‐Cbfβ in osteosarcoma cells. Journal of Cellular Physiology. 221(3). 560–571. 49 indexed citations

11.

Visser, W. Edward, Jurgen Jansen, Edith C. H. Friesema, et al.. (2008). Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations. Human Mutation. 30(1). 29–38. 57 indexed citations

12.

Mancilla, Edna E., et al.. (2007). L‐type calcium channels in growth plate chondrocytes participate in endochondral ossification. Journal of Cellular Biochemistry. 101(2). 389–398. 14 indexed citations

13.

Friesema, Edith C. H., Annette Grueters, Heike Biebermann, et al.. (2004). Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation. The Lancet. 364(9443). 1435–1437. 512 indexed citations breakdown →

14.

Mancilla, Edna E., Helena Poggi, Gabriela M. Repetto, et al.. (2003). Y Chromosome Sequences in Turner's Syndrome: Association with Virilization and Gonadoblastoma. Journal of Pediatric Endocrinology and Metabolism. 16(8). 1157–63. 26 indexed citations

15.

Luca, Francesco De, Jennifer A. Uyeda, Verónica Mericq, et al.. (2000). Retinoic Acid Is a Potent Regulator of Growth Plate Chondrogenesis. Endocrinology. 141(1). 346–353. 74 indexed citations

16.

Stock, John L., Rosalind S. Brown, Jeffrey Baron, et al.. (1999). Autosomal Dominant Hypoparathyroidism Associated with Short Stature and Premature Osteoarthritis¹. The Journal of Clinical Endocrinology & Metabolism. 84(9). 3036–3040. 14 indexed citations

17.

Mancilla, Edna E., et al.. (1998). Activating Mutations of the Ca2+-Sensing Receptor. Molecular Genetics and Metabolism. 64(3). 198–204. 15 indexed citations

18.

Luca, Francesco De, Kausik K. Ray, Edna E. Mancilla, et al.. (1997). Sporadic Hypoparathyroidism Caused byde NovoGain- of-Function Mutations of the Ca²⁺-Sensing Receptor¹. The Journal of Clinical Endocrinology & Metabolism. 82(8). 2710–2715. 71 indexed citations

19.

Mancilla, Edna E., Francesco De Luca, Kausik K. Ray, et al.. (1997). A Ca2+-Sensing Receptor Mutation Causes Hypoparathyroidism by Increasing Receptor Sensitivity to Ca2+ and Maximal Signal Transduction1. Pediatric Research. 42(4). 443–447. 26 indexed citations

20.

Mancilla, Edna E., et al.. (1990). Quinine blocks the high conductance, calcium‐activated potassium channel in rat pancreatic β‐cells. FEBS Letters. 260(1). 105–108. 24 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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