Staci Kallish

569 total citations
14 papers, 103 citations indexed

About

Staci Kallish is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Staci Kallish has authored 14 papers receiving a total of 103 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Physiology. Recurrent topics in Staci Kallish's work include Glycogen Storage Diseases and Myoclonus (2 papers), Genomics and Rare Diseases (2 papers) and BRCA gene mutations in cancer (2 papers). Staci Kallish is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (2 papers), Genomics and Rare Diseases (2 papers) and BRCA gene mutations in cancer (2 papers). Staci Kallish collaborates with scholars based in United States, Canada and Italy. Staci Kallish's co-authors include Paige Kaplan, Charles A. Stanley, Jie Chen, Andrew Palladino, Malcolm J. Bennett, Scott P. Bartlett, Mieke M. van Haelst, James A. Katowitz, Elaine H. Zackai and Donna M. McDonald‐McGinn and has published in prestigious journals such as The American Journal of Human Genetics, Molecular Genetics and Metabolism and European Journal of Pediatrics.

In The Last Decade

Staci Kallish

11 papers receiving 101 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Staci Kallish United States	6	46	32	29	19	14	14	103
Aisha Al Shamsi United Arab Emirates	6	67 1.5×	35 1.1×	20 0.7×	18 0.9×	4 0.3×	13	129
Wagner Antonio da Rosa Baratela Brazil	8	61 1.3×	62 1.9×	32 1.1×	8 0.4×	4 0.3×	14	153
Karin van Spaendonck‐Zwarts Netherlands	4	63 1.4×	45 1.4×	20 0.7×	6 0.3×	33 2.4×	5	126
Jessica L. Schneller United States	6	87 1.9×	48 1.5×	23 0.8×	41 2.2×	3 0.2×	6	139
Alya Al-Shakaki Qatar	4	131 2.8×	87 2.7×	21 0.7×	7 0.4×	10 0.7×	7	217
Gudny A. Arnadottir Iceland	5	47 1.0×	34 1.1×	7 0.2×	8 0.4×	12 0.9×	8	124
Hisaya Kato Japan	8	73 1.6×	14 0.4×	21 0.7×	4 0.2×	3 0.2×	25	126
Rob Hastings United Kingdom	5	94 2.0×	26 0.8×	8 0.3×	24 1.3×	29 2.1×	9	136
Laura Konczal United States	6	77 1.7×	119 3.7×	13 0.4×	30 1.6×	5 0.4×	13	185
Francesco Puzzo United States	7	103 2.2×	82 2.6×	50 1.7×	7 0.4×	11 0.8×	14	176

Countries citing papers authored by Staci Kallish

Since Specialization

Citations

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

Fields of papers citing papers by Staci Kallish

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Staci Kallish

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

All Works

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14 of 14 papers shown

Gold, Jessica I., Nina B. Gold, Anna Raper, et al.. (2025). Racial and socioeconomic disparities in genetic evaluation and testing in the adult patient population. The American Journal of Human Genetics. 113(1). 29–40.

Patel, Namrata, Allyson M. Pishko, Ethan M. Weinberg, et al.. (2025). Evaluation of a screening protocol for telomere biology disorders in individuals with interstitial lung disease undergoing lung transplant evaluation. ERJ Open Research. 11(5). 875–2024.

Conway, Laura, et al.. (2024). Unraveling a history of overlap: A phenotypic comparison of RBCK1‐related disease and glycogen storage disease type IV. American Journal of Medical Genetics Part A. 194(7). e63574–e63574. 1 indexed citations

Egleston, Brian L., Lily Hoffman‐Andrews, H Griffin, et al.. (2024). Facilitating return of actionable genetic research results from a biobank repository: Participant uptake and utilization of digital interventions. Human Genetics and Genomics Advances. 5(4). 100346–100346.

Bichet, Daniel G., Robert J. Hopkin, Sridhar R. Allam, et al.. (2023). Consensus recommendations for the treatment and management of patients with Fabry disease on migalastat: a modified Delphi study. Frontiers in Medicine. 10. 1220637–1220637. 10 indexed citations

Priestley, Jessica, et al.. (2023). Unmasking the challenges of Kabuki syndrome in adulthood: A case series. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 193(2). 128–138. 1 indexed citations

Turin, Christie G., Kyu Sang Joeng, Staci Kallish, et al.. (2021). Heterozygous variant in WNT1 gene in two brothers with early onset osteoporosis. Bone Reports. 15. 101118–101118. 3 indexed citations

Kaplan, Frederick S., Jay C. Groppe, Meiqi Xu, et al.. (2021). An ACVR1^R375P pathogenic variant in two families with mild fibrodysplasia ossificans progressiva. American Journal of Medical Genetics Part A. 188(3). 806–817. 5 indexed citations

Kahn, Benjamin, Sokratis A. Apostolidis, Allison R. Greenplate, et al.. (2021). Multisystem Inflammation and Organ Dysfunction After BNT162b2 Messenger RNA Coronavirus Disease 2019 Vaccination. Critical Care Explorations. 3(11). e0578–e0578. 13 indexed citations

10.

Kallish, Staci, et al.. (2018). Mitral valve prolapse and aortic root dilation in adults with hypermobile Ehlers–Danlos syndrome and related disorders. American Journal of Medical Genetics Part A. 176(9). 1838–1844. 19 indexed citations

11.

Unolt, Marta, M. Cristina Digilio, Bruno Marino, et al.. (2018). Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome. European Journal of Medical Genetics. 61(7). 411–415. 3 indexed citations

12.

Kallish, Staci & Paige Kaplan. (2012). A disease severity scoring system for children with type 1 Gaucher disease. European Journal of Pediatrics. 172(1). 39–43. 11 indexed citations

13.

Palladino, Andrew, Jie Chen, Staci Kallish, Charles A. Stanley, & Malcolm J. Bennett. (2012). Measurement of tissue acyl-CoAs using flow-injection tandem mass spectrometry: acyl-CoA profiles in short-chain fatty acid oxidation defects. Molecular Genetics and Metabolism. 107(4). 679–683. 27 indexed citations

14.

Kallish, Staci, Donna M. McDonald‐McGinn, Mieke M. van Haelst, et al.. (2011). Ablepharon–Macrostomia syndrome—Extension of the phenotype. American Journal of Medical Genetics Part A. 155(12). 3060–3062. 10 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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