Angelika Erwin

1.3k total citations · 1 hit paper
31 papers, 646 citations indexed

About

Angelika Erwin is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Angelika Erwin has authored 31 papers receiving a total of 646 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 14 papers in Pediatrics, Perinatology and Child Health and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Angelika Erwin's work include Porphyrin Metabolism and Disorders (14 papers), Heme Oxygenase-1 and Carbon Monoxide (11 papers) and Neonatal Health and Biochemistry (9 papers). Angelika Erwin is often cited by papers focused on Porphyrin Metabolism and Disorders (14 papers), Heme Oxygenase-1 and Carbon Monoxide (11 papers) and Neonatal Health and Biochemistry (9 papers). Angelika Erwin collaborates with scholars based in United States, Australia and Argentina. Angelika Erwin's co-authors include Robert J. Desnick, Ashwani K. Singal, Habeeb Salameh, J.S. Dungan, Robert G. Best, Charis Eng, Susan Klugman, Sandra Darilek, Kristin G. Monaghan and Jennifer Malinowski and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gastroenterology and Journal of the American College of Cardiology.

In The Last Decade

Angelika Erwin

28 papers receiving 636 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.

Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)

2022 101 citations J.S. Dungan, Susan Klugman et al. Genetics in Medicine profile →

Peers

Countries citing papers authored by Angelika Erwin

Since Specialization

Citations

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

Fields of papers citing papers by Angelika Erwin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angelika Erwin

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

#	Work	Indexed citations
1	Contemporary Multimodality Imaging for Diagnosis and Management of Fabry Cardiomyopathy 2024 ·Journal of Clinical Medicine ·Simrat Kaur, Jaideep Singh Bhalla, Angelika Erwin, Wael A. Jaber, Tom Kai Ming Wang	1
2	Congenital erythropoietic porphyria 2024 ·Liver International ·Jordi To‐Figueras, Angelika Erwin, Paula Aguilera, Óscar Millet, Robert J. Desnick	2
3	SEX BASED DIFFERENCES IN CARDIAC MANIFESTATIONS OF FABRY DISEASE USING MODERN CARDIAC IMAGING 2024 ·Journal of the American College of Cardiology ·Simrat Kaur, Fatimah Chamseddine, Aldo L. Schenone, Angelika Erwin, (unknown), Wael A. Jaber	0
4	Integration of a pharmacist-led pharmacogenomic service in a geriatric clinic: Barriers and outcomes 2023 ·Journal of the American Pharmacists Association ·(unknown), (unknown), (unknown), Ardeshir Z. Hashmi, Angelika Erwin, (unknown), Jennifer Hockings	5
5	Prevalence of Undiagnosed Acute Hepatic Porphyria in Cyclic Vomiting Syndrome and Overlap in Clinical Symptoms 2022 ·Digestive Diseases and Sciences ·(unknown), (unknown), Emma Garacci, Angelika Erwin, Thangam Venkatesan	6
6	Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG) breakdown → 2022 ·Genetics in Medicine ·J.S. Dungan, Susan Klugman, Sandra Darilek, Jennifer Malinowski, Yassmine Akkari, Kristin G. Monaghan, Angelika Erwin, Robert G. Best	101
7	Porphyrias in the Age of Targeted Therapies 2021 ·Diagnostics ·Angelika Erwin, Manisha Balwani	9
8	Higher iron stores and the HFE 187C>G variant delay onset of peripheral neuropathy during combination antiretroviral therapy 2020 ·PLoS ONE ·Asha Kallianpur, Wanqing Wen, Angelika Erwin, David B. Clifford, Todd Hulgan, Gregory K. Robbins	3
9	Pharmacogenomics: An evolving clinical tool for precision medicine 2020 ·Cleveland Clinic Journal of Medicine ·Jennifer Hockings, Amy L. Pasternak, Angelika Erwin, Neil Mason, Charis Eng, J. Kevin Hicks	39
10	Chromosome 3p Inverted Duplication with Terminal Deletion: Second Postnatal Case Report with Additional Clinical Features 2019 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), (unknown), Angelika Erwin, (unknown), Caroline Astbury	1
11	Evaluating the Patient-Reported Outcomes Measurement Information System scales in acute intermittent porphyria 2019 ·Genetics in Medicine ·Hetanshi Naik, Jessica Overbey, Guy H. Montgomery, Gary Winkel, Manisha Balwani, Karl E. Anderson, D. Montgomery Bissell, Herbert L. Bonkovsky, John D. Phillips, Bruce Wang, Brendan M. McGuire, Sioḃán Keel, Cynthia Levy, Angelika Erwin, Robert J. Desnick	8
12	Identification and characterization of 40 novel hydroxymethylbilane synthase mutations that cause acute intermittent porphyria 2019 ·Journal of Inherited Metabolic Disease ·Brenden Chen, (unknown), Angelika Erwin, Manisha Balwani, Irina Nazarenko, John D. Phillips, Robert J. Desnick, Makiko Yasuda	16
13	Congenital erythropoietic porphyria: Recent advances 2018 ·Molecular Genetics and Metabolism ·Angelika Erwin, Robert J. Desnick	33
14	Identification and characterization of 40 novel hydroxymethylbilane synthase mutations that cause acute intermittent porphyria 2018 ·Journal of Inherited Metabolic Disease ·Brenden Chen, (unknown), Angelika Erwin, Manisha Balwani, (unknown), John D. Phillips, Robert J. Desnick, Makiko Yasuda	2
15	The role of sebelipase alfa in the treatment of lysosomal acid lipase deficiency 2017 ·Therapeutic Advances in Gastroenterology ·Angelika Erwin	18
16	PNPLA3 as a Genetic Determinant of Risk for and Severity of Non-alcoholic Fatty Liver Disease Spectrum 2016 ·Journal of Clinical and Translational Hepatology ·Habeeb Salameh, (unknown), (unknown), (unknown), (unknown), Angelika Erwin, Ashwani K. Singal	38
17	Congenital Erythropoietic Porphyria 2016 ·Angelika Erwin, Manisha Balwani, Robert J. Desnick	1
18	Prophylactic immune modulation in infantile Ρompe disease using low-dose methotrexate induction: A safe, inexpensive, widely accessible, and efficacious strategy 2016 ·Molecular Genetics and Metabolism ·Zoheb B. Kazi, Ankit K. Desai, Angelika Erwin, (unknown), (unknown), David Kronn, Seymour Packman, M.G. Sabbadini, Jean‐Marc Nuoffer, James D. Weisfeld‐Adams, William B. Rizzo, Clarisa Maxit, Marianne Rohrbach, Diana Ballhausen, (unknown), Omar Abdul‐Rahman, Alexandra Joseph, Alison McVie‐Wylie, Susan Richards, Priya S. Kishnani	3
19	Liver Transplantation for Acute Intermittent Porphyria: Biochemical and Pathologic Studies of the Explanted Liver 2015 ·Molecular Medicine ·Makiko Yasuda, Angelika Erwin, Lawrence U. Liu, Manisha Balwani, Brenden Chen, (unknown), Lin Gan, Maria Isabel Fiel, Ronald E. Gordon, Chunli Yu, Sonia Clavero, Antonios Arvelakis, Hetanshi Naik, (unknown), John D. Phillips, Karl E. Anderson, (unknown), Sander Florman, Robert J. Desnick	44
20	PNPLA3 Gene Polymorphism Is Associated With Predisposition to and Severity of Alcoholic Liver Disease 2015 ·The American Journal of Gastroenterology ·Habeeb Salameh, Evan Raff, Angelika Erwin, Devanshi Seth, Hans Dieter Nischalke, Edmondo Falleti, Maria Antonella Burza, (unknown), Stefano Romeo, Antonio Molinaro, Stefano Ginanni Corradini, Pierluigi Toniutto, Ulrich Spengler, Ann K. Daly, Christopher P. Day, Yong‐Fang Kuo, Ashwani K. Singal	120

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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