Alexander Ing

1.1k total citations
16 papers, 314 citations indexed

About

Alexander Ing is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Alexander Ing has authored 16 papers receiving a total of 314 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Alexander Ing's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and RNA regulation and disease (2 papers). Alexander Ing is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and RNA regulation and disease (2 papers). Alexander Ing collaborates with scholars based in United States, Singapore and United Kingdom. Alexander Ing's co-authors include Roddy Walsh, Stuart A. Cook, Nicola Whiffin, James S. Ware, Eric Vallabh Minikel, Konrad J. Karczewski, Daniel G. MacArthur, Paul J.R. Barton, Birgit Funke and Anne O’Donnell‐Luria and has published in prestigious journals such as Blood, Genetics in Medicine and JAMA Cardiology.

In The Last Decade

Alexander Ing

15 papers receiving 314 citations

Peers

Alexander Ing

GENET

CCM

PFM

Ruolan Guo China

Valerie K. Jordan United States

Gundula Povysil United States

Julie A. Jurgens United States

Stefanie Engert Germany

Jie‐Yuan Jin China

Amali Mallawaarachchi Australia

Johanna C. Herkert Netherlands

Yu Ding China

Ruolan Guo China

Alexander Ing

120 ×0.8

GENET

158 ×1.1

50 ×0.5

CCM

48 ×1.7

24 ×1.2

PFM

Citations per year, relative to Alexander Ing Alexander Ing (= 1×) peers Ruolan Guo

Countries citing papers authored by Alexander Ing

Since Specialization

Citations

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

Fields of papers citing papers by Alexander Ing

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Ing

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

All Works

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16 of 16 papers shown

Miller, Charles M., et al.. (2025). Genetic testing results of retinal dystrophies in a diverse population: impact of race and ethnicity. Ophthalmic Genetics. 46(2). 160–165. 1 indexed citations

Ranaivo, Hantamalala Ralay, et al.. (2024). Ophthalmic Manifestations in a Diverse Pediatric Population with Type I and Type II Stickler Syndrome. Ophthalmology Retina. 9(7). 690–698. 1 indexed citations

Yap, Kai Lee, Alexander Ing, Allan Gordon, et al.. (2024). A Case of Non-Syndromic Congenital Cataracts Caused by a Novel MAF Variant in the C-Terminal DNA-Binding Domain—Case Report and Literature Review. Genes. 15(6). 686–686.

Bohnsack, Brenda L., Alexander Ing, Hantamalala Ralay Ranaivo, et al.. (2024). Ocular manifestations of CHARGE syndrome in a pediatric cohort with genotype/phenotype analysis. American Journal of Medical Genetics Part A. 194(8). e63618–e63618. 2 indexed citations

Kuntz, Nancy L., et al.. (2023). Expansion of the phenotypic spectrum associated with pathogenic missense variation in DHX16. American Journal of Medical Genetics Part A. 194(1). 53–58. 2 indexed citations

Bohnsack, Brenda L., et al.. (2023). Evaluation of Genetic Testing in a Cohort of Diverse Pediatric Patients in the United States with Congenital Cataracts. Genes. 14(3). 608–608. 4 indexed citations

Bohnsack, Brenda L., et al.. (2023). Diagnostic Yield of Genetic Testing for Ocular and Oculocutaneous Albinism in a Diverse United States Pediatric Population. Genes. 14(1). 135–135. 3 indexed citations

Charrow, Joel, et al.. (2022). Utility and Outcomes of the 2019 American College of Medical Genetics and Genomics–Clinical Genome Resource Guidelines for Interpretation of Copy Number Variants with Borderline Classifications at an Academic Clinical Diagnostic Laboratory. Journal of Molecular Diagnostics. 24(10). 1100–1111. 4 indexed citations

Ing, Alexander, et al.. (2022). eP363: A review of characteristic features identifying balanced chromosomal translocations with increased potential for 3:1 meiotic segregation. Genetics in Medicine. 24(3). S228–S229. 1 indexed citations

10.

Ing, Alexander, et al.. (2021). Novel compound heterozygous variants of TBXAS1 presenting with Ghosal hematodiaphyseal dysplasia treated with steroids. Molecular Genetics & Genomic Medicine. 9(3). e1494–e1494. 4 indexed citations

11.

Ing, Alexander, Dawn A. Kirschmann, Christopher J. McCabe, et al.. (2021). Transcript analysis for variant classification resolution in a child with primary ciliary dyskinesia. Molecular Case Studies. 7(1). a005363–a005363. 2 indexed citations

12.

Webster, Gregory, Megan J. Puckelwartz, Lorenzo L. Pesce, et al.. (2021). Genomic Autopsy of Sudden Deaths in Young Individuals. JAMA Cardiology. 6(11). 1247–1247. 23 indexed citations

13.

Webster, Gregory, Elhadi H. Aburawi, Marie Chaix, et al.. (2020). Life-threatening arrhythmias with autosomal recessive TECRL variants. EP Europace. 23(5). 781–788. 18 indexed citations

14.

Ing, Alexander, Kai Lee Yap, Sherif M. Badawy, et al.. (2019). Probably Pathogenic KMT2D Variants Presenting with Cytopenias and Primary Immune Deficiency. Blood. 134(Supplement_1). 2334–2334. 1 indexed citations

15.

Whiffin, Nicola, Eric Vallabh Minikel, Roddy Walsh, et al.. (2017). Using high-resolution variant frequencies to empower clinical genome interpretation. Genetics in Medicine. 19(10). 1151–1158. 245 indexed citations

16.

Ing, Alexander, et al.. (2017). LB-MAP: Load-Balanced Middlebox Assignment in Policy-Driven Data Centers. 18. 1–9. 3 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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