Alyssa Ritter

859 total citations
20 papers, 229 citations indexed

About

Alyssa Ritter is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Alyssa Ritter has authored 20 papers receiving a total of 229 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Cardiology and Cardiovascular Medicine and 5 papers in Genetics. Recurrent topics in Alyssa Ritter's work include Congenital heart defects research (7 papers), Cardiomyopathy and Myosin Studies (5 papers) and Genomics and Rare Diseases (3 papers). Alyssa Ritter is often cited by papers focused on Congenital heart defects research (7 papers), Cardiomyopathy and Myosin Studies (5 papers) and Genomics and Rare Diseases (3 papers). Alyssa Ritter collaborates with scholars based in United States, Canada and Australia. Alyssa Ritter's co-authors include Kosuke Izumi, Rebecca C. Ahrens‐Nicklas, Kimberly Y. Lin, Līvija Medne, Ian D. Krantz, John A. Gardner, Justin H. Berger, Emma Bedoukian, Matthew A. Deardorff and Joseph W. Rossano and has published in prestigious journals such as The American Journal of Human Genetics, Science Advances and Clinical Chemistry.

In The Last Decade

Alyssa Ritter

20 papers receiving 224 citations

Peers

Alyssa Ritter
Sophie Julia France
Şükrü Candan Türkiye
Eric Arruda Canada
Shu Yau United Kingdom
Neda Zadeh United States
Ivy Ng Singapore
Kathryn M. Shively United States
Lucie Gueneau France
Jean‐Marie Rival France
Rie Kawamura Japan
Sophie Julia France
Alyssa Ritter
Citations per year, relative to Alyssa Ritter Alyssa Ritter (= 1×) peers Sophie Julia

Countries citing papers authored by Alyssa Ritter

Since Specialization
Citations

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

Fields of papers citing papers by Alyssa Ritter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alyssa Ritter

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

All Works

20 of 20 papers shown
1.
Stephens, Paul, Renzo Calderón-Anyosa, Danielle S. Burstein, et al.. (2023). Electrocardiographic Findings in Genotype-Positive and Non-sarcomeric Children with Definite Hypertrophic Cardiomyopathy and Subclinical Variant Carriers. Pediatric Cardiology. 45(8). 1784–1797. 2 indexed citations
2.
Ritter, Alyssa, Jacqueline Leonard, Christopher Gray, et al.. (2022). MYH7 variants cause complex congenital heart disease. American Journal of Medical Genetics Part A. 188(9). 2772–2776. 6 indexed citations
3.
Hong, Xinying, et al.. (2021). Fine-Tuning 3-Methylglutaconic Aciduria Cutoffs for a Patient with Infantile-Onset Barth Syndrome. Clinical Chemistry. 68(2). 365–367. 1 indexed citations
4.
Burstein, Danielle S., J. William Gaynor, Heather Griffis, et al.. (2020). Genetic variant burden and adverse outcomes in pediatric cardiomyopathy. Pediatric Research. 89(6). 1470–1476. 14 indexed citations
5.
Cohen, Jennifer L., Samantha A. Schrier Vergano, Alanna Strong, et al.. (2020). EP300‐related Rubinstein–Taybi syndrome: Highlighted rare phenotypic findings and a genotype–phenotype meta‐analysis of 74 patients. American Journal of Medical Genetics Part A. 182(12). 2926–2938. 18 indexed citations
6.
Ahrens‐Nicklas, Rebecca C., Renzo Calderón-Anyosa, Alyssa Ritter, et al.. (2020). Genotype–phenotype association by echocardiography offers incremental value in patients with Noonan Syndrome with Multiple Lentigines. Pediatric Research. 90(2). 444–451. 9 indexed citations
7.
Li, Dong, Rebecca C. Ahrens‐Nicklas, Janice Baker, et al.. (2020). The variability of SMARCA4‐related Coffin–Siris syndrome: Do nonsense candidate variants add to milder phenotypes?. American Journal of Medical Genetics Part A. 182(9). 2058–2067. 14 indexed citations
8.
Ritter, Alyssa, Justin H. Berger, Matthew A. Deardorff, et al.. (2020). Variants in NAA15 cause pediatric hypertrophic cardiomyopathy. American Journal of Medical Genetics Part A. 185(1). 228–233. 11 indexed citations
9.
Ritter, Alyssa, Petra Werner, Avni Santani, et al.. (2020). NKX2‐6 related congenital heart disease: Biallelic homeodomain‐disrupting variants and truncus arteriosus. American Journal of Medical Genetics Part A. 182(6). 1454–1459. 6 indexed citations
10.
Ritter, Alyssa, Emma Bedoukian, Justin H. Berger, et al.. (2019). Clinical utility of exome sequencing in infantile heart failure. Genetics in Medicine. 22(2). 423–426. 13 indexed citations
11.
Ritter, Alyssa, et al.. (2019). Interstitial 4q Deletion Syndrome Including <b><i>NR3C2</i></b> Causing Pseudohypoaldosteronism. Molecular Syndromology. 10(6). 327–331. 4 indexed citations
12.
Nixon, Kevin C., Justine Rousseau, Sophie Ehresmann, et al.. (2019). A Syndromic Neurodevelopmental Disorder Caused by Mutations in SMARCD1, a Core SWI/SNF Subunit Needed for Context-Dependent Neuronal Gene Regulation in Flies. The American Journal of Human Genetics. 104(4). 596–610. 27 indexed citations
13.
Ritter, Alyssa, Karl Degenhardt, Stefanie B. Kasperski, et al.. (2019). Fetal cardiomyopathy in neurofibromatosis type I: Novel phenotype and review of the literature. American Journal of Medical Genetics Part A. 179(6). 1042–1046. 2 indexed citations
14.
Ahrens‐Nicklas, Rebecca C., Christopher T. Pappas, Gerrie P. Farman, et al.. (2019). Disruption of cardiac thin filament assembly arising from a mutation in LMOD2 : A novel mechanism of neonatal dilated cardiomyopathy. Science Advances. 5(9). eaax2066–eaax2066. 34 indexed citations
15.
Ritter, Alyssa, Eric J. Granquist, V. Ramesh Iyer, & Kosuke Izumi. (2018). Cardiac Fibroma with Ventricular Tachycardia: An Unusual Clinical Presentation of Nevoid Basal Cell Carcinoma Syndrome. Molecular Syndromology. 9(4). 219–223. 5 indexed citations
16.
Ritter, Alyssa, Carey McDougall, Cara Skraban, et al.. (2018). Variable Clinical Manifestations of Xia‐Gibbs syndrome: Findings of Consecutively Identified Cases at a Single Children's Hospital. American Journal of Medical Genetics Part A. 176(9). 1890–1896. 24 indexed citations
17.
Iwata‐Otsubo, Aiko, et al.. (2017). DOCK3‐related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotonia. American Journal of Medical Genetics Part A. 176(1). 241–245. 12 indexed citations
18.
Ritter, Alyssa, Carrie Atzinger, J. Howard James, et al.. (2017). Natural history of aortic root dilation through young adulthood in a hypermobile Ehlers–Danlos syndrome cohort. American Journal of Medical Genetics Part A. 173(6). 1467–1472. 13 indexed citations
19.
Ritter, Alyssa, Stefan Egger, & Martin Emesz. (2012). Dirofilariose. Der Ophthalmologe. 109(8). 788–790. 5 indexed citations
20.
Ritter, Alyssa & John A. Gardner. (1971). Pseudopotential Calculation of Knight-Shift Temperature and Volume Dependence in Liquid and Solid Sodium. Physical review. B, Solid state. 3(1). 46–49. 9 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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