Mallory Owen

508 total citations
8 papers, 103 citations indexed

About

Mallory Owen is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Mallory Owen has authored 8 papers receiving a total of 103 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Mallory Owen's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Neonatal Respiratory Health Research (2 papers). Mallory Owen is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Neonatal Respiratory Health Research (2 papers). Mallory Owen collaborates with scholars based in United States. Mallory Owen's co-authors include Stephen F. Kingsmore, Christina Chambers, Michelle M. Clark, Christian Holm Hansen, David Dimmock, Rebecca J. Baer, Gretchen Bandoli, Charlotte A. Hobbs, Elizabeth Kiernan and Yan Ding and has published in prestigious journals such as Journal of Neurology Neurosurgery & Psychiatry, JAMA Network Open and Prenatal Diagnosis.

In The Last Decade

Mallory Owen

8 papers receiving 103 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mallory Owen United States	5	66	27	25	15	15	8	103
Sara Caylor United States	4	109 1.7×	44 1.6×	34 1.4×	22 1.5×	13 0.9×	4	139
Joanna Lazier Canada	8	67 1.0×	46 1.7×	55 2.2×	10 0.7×	7 0.5×	19	126
Katharina Löhner Netherlands	4	87 1.3×	59 2.2×	28 1.1×	19 1.3×	5 0.3×	5	137
Michelle Steinraths Canada	8	104 1.6×	60 2.2×	60 2.4×	23 1.5×	13 0.9×	12	168
Jasmine Lee Fong Fung China	7	122 1.8×	49 1.8×	48 1.9×	15 1.0×	14 0.9×	15	167
Cecelia P. Tamburro United States	4	86 1.3×	54 2.0×	8 0.3×	9 0.6×	14 0.9×	4	133
Grace E. VanNoy United States	8	155 2.3×	72 2.7×	47 1.9×	36 2.4×	22 1.5×	15	232
Clara Yujing Cheong Singapore	8	46 0.7×	110 4.1×	36 1.4×	12 0.8×	19 1.3×	12	161
Helen Dolling United Kingdom	2	130 2.0×	52 1.9×	32 1.3×	28 1.9×	8 0.5×	3	159
Aurélie Coussement France	7	67 1.0×	40 1.5×	38 1.5×	26 1.7×	7 0.5×	16	141

Countries citing papers authored by Mallory Owen

Since Specialization

Citations

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

Fields of papers citing papers by Mallory Owen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mallory Owen

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

All Works

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8 of 8 papers shown

Owen, Mallory, Meredith S. Wright, Serge Batalov, et al.. (2023). Reclassification of the Etiology of Infant Mortality With Whole-Genome Sequencing. JAMA Network Open. 6(2). e2254069–e2254069. 22 indexed citations

Owen, Mallory, Serge Batalov, Katarzyna A. Ellsworth, et al.. (2023). Rapid Whole Genome Sequencing for Diagnosis of Single Locus Genetic Diseases in Critically Ill Children. Methods in molecular biology. 2621. 217–239. 3 indexed citations

Ding, Yan, Mallory Owen, Jennie Le, et al.. (2023). Scalable, high quality, whole genome sequencing from archived, newborn, dried blood spots. npj Genomic Medicine. 8(1). 5–5. 14 indexed citations

Owen, Mallory, et al.. (2022). Retrospective identification of prenatal fetal anomalies associated with diagnostic neonatal genomic sequencing results. Prenatal Diagnosis. 42(6). 705–716. 3 indexed citations

Grunseich, Christopher, Mallory Owen, Alice B. Schindler, et al.. (2021). Improving the efficacy of exome sequencing at a quaternary care referral centre: novel mutations, clinical presentations and diagnostic challenges in rare neurogenetic diseases. Journal of Neurology Neurosurgery & Psychiatry. 92(11). 1186–1196. 12 indexed citations

Owen, Mallory, Jerica Lenberg, Annette Feigenbaum, et al.. (2021). Postmortem whole-genome sequencing on a dried blood spot identifies a novel homozygous SUOX variant causing isolated sulfite oxidase deficiency. Molecular Case Studies. 7(3). a006091–a006091. 4 indexed citations

Bandoli, Gretchen, Rebecca J. Baer, Mallory Owen, et al.. (2021). Maternal, infant, and environmental risk factors for sudden unexpected infant deaths: results from a large, administrative cohort. The Journal of Maternal-Fetal & Neonatal Medicine. 35(25). 8998–9005. 11 indexed citations

Kingsmore, Stephen F., Mallory Owen, Michelle M. Clark, et al.. (2020). Measurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing. npj Genomic Medicine. 5(1). 49–49. 34 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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