Amy Hietala

728 total citations
7 papers, 137 citations indexed

About

Amy Hietala is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Amy Hietala has authored 7 papers receiving a total of 137 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 5 papers in Physiology. Recurrent topics in Amy Hietala's work include Metabolism and Genetic Disorders (5 papers), Peroxisome Proliferator-Activated Receptors (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Amy Hietala is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Peroxisome Proliferator-Activated Receptors (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Amy Hietala collaborates with scholars based in United States and France. Amy Hietala's co-authors include Amy Gaviglio, Kyriakie Sarafoglou, William Thomas, Mark McCann, Weston P. Miller, Heather Zierhut, Katie M. Wiens, Daniel Kenney‐Jung, Paul J. Orchard and Ashish O. Gupta and has published in prestigious journals such as PEDIATRICS, The Journal of Pediatrics and Molecular Genetics and Metabolism.

In The Last Decade

Amy Hietala

7 papers receiving 136 citations

Peers

Amy Hietala

MB

CB

EDM

HEMAT

UROLO

V. Reid Sutton United States

Jozef Hertecant United Arab Emirates

Flávia Piazzon Brazil

Ghunwa Nakouzi United States

Marietta Truger Germany

Mari‐Anne Vals Estonia

Doreen Meissner South Africa

Takuya Fushimi Japan

Athanasia Stoupa France

Ali Alothaim Saudi Arabia

V. Reid Sutton United States

Amy Hietala

120 ×1.1

MB

109 ×1.2

CB

10 ×0.3

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5 ×0.2

HEMAT

14 ×0.8

UROLO

Citations per year, relative to Amy Hietala Amy Hietala (= 1×) peers V. Reid Sutton

Countries citing papers authored by Amy Hietala

Since Specialization

Citations

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

Fields of papers citing papers by Amy Hietala

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amy Hietala

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

All Works

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7 of 7 papers shown

1.

Dizikes, George J., C. Austin Pickens, Carla Cuthbert, et al.. (2023). Harmonization of Newborn Screening Results for Pompe Disease and Mucopolysaccharidosis Type I. International Journal of Neonatal Screening. 9(1). 11–11. 5 indexed citations

2.

Pillai, Nishitha R., Alia Ahmed, Amy Hietala, et al.. (2023). Disparities in late and lost: Pediatricians' role in following Pompe disease identified by newborn screening. Molecular Genetics and Metabolism. 140(1-2). 107633–107633. 2 indexed citations

3.

Conti, Brian J., et al.. (2022). Newborn Screen for X-Linked Adrenoleukodystrophy Using Flow Injection Tandem Mass Spectrometry in Negative Ion Mode. International Journal of Neonatal Screening. 8(2). 27–27. 2 indexed citations

4.

Wiens, Katie M., Susan A. Berry, Amy Gaviglio, et al.. (2019). A report on state‐wide implementation of newborn screening for X‐linked Adrenoleukodystrophy. American Journal of Medical Genetics Part A. 179(7). 1205–1213. 51 indexed citations

5.

Wiens, Katie M., Amy Gaviglio, Ashish O. Gupta, et al.. (2019). A report on state-wide implementation of newborn screening for X-linked adrenoleukodystrophy. Yearbook of pediatric endocrinology. 1 indexed citations

6.

Sarafoglou, Kyriakie, et al.. (2014). Comparison of Newborn Screening Protocols for Congenital Adrenal Hyperplasia in Preterm Infants. The Journal of Pediatrics. 164(5). 1136–1140. 23 indexed citations

7.

Sarafoglou, Kyriakie, et al.. (2012). Comparison of One-Tier and Two-Tier Newborn Screening Metrics for Congenital Adrenal Hyperplasia. PEDIATRICS. 130(5). e1261–e1268. 53 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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