Sarah Soden

3.1k total citations
30 papers, 705 citations indexed

About

Sarah Soden is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Sarah Soden has authored 30 papers receiving a total of 705 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 10 papers in Pediatrics, Perinatology and Child Health and 6 papers in Molecular Biology. Recurrent topics in Sarah Soden's work include Genomics and Rare Diseases (10 papers), Pharmacogenetics and Drug Metabolism (5 papers) and Pharmaceutical studies and practices (5 papers). Sarah Soden is often cited by papers focused on Genomics and Rare Diseases (10 papers), Pharmacogenetics and Drug Metabolism (5 papers) and Pharmaceutical studies and practices (5 papers). Sarah Soden collaborates with scholars based in United States, Italy and Germany. Sarah Soden's co-authors include Neil Miller, Carol Saunders, Emily Farrow, Stephen F. Kingsmore, Darrell L. Dinwiddie, Laurie D. Smith, Jennifer A. Lowry, John D. Lantos, Isabelle Thiffault and Gary S. Wasserman and has published in prestigious journals such as Clinical Pharmacology & Therapeutics, The Journal of General Physiology and Neurobiology of Disease.

In The Last Decade

Sarah Soden

29 papers receiving 697 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarah Soden United States 16 330 303 94 87 70 30 705
Kira Apse United States 12 215 0.7× 261 0.9× 208 2.2× 20 0.2× 46 0.7× 16 798
Xueqing Qian China 11 131 0.4× 269 0.9× 49 0.5× 25 0.3× 57 0.8× 25 537
Alex E. Felice Malta 16 129 0.4× 270 0.9× 132 1.4× 23 0.3× 30 0.4× 59 1.0k
Miquel Tuson Spain 10 269 0.8× 571 1.9× 88 0.9× 151 1.7× 86 1.2× 14 880
Mehmet Seven Türkiye 15 115 0.3× 304 1.0× 265 2.8× 21 0.2× 196 2.8× 59 765
Paula Garcia Portugal 16 195 0.6× 344 1.1× 81 0.9× 9 0.1× 90 1.3× 49 774
Yasuhiro Naiki Japan 16 356 1.1× 510 1.7× 106 1.1× 81 0.9× 9 0.1× 39 918
Stefan Wolking Germany 12 56 0.2× 121 0.4× 110 1.2× 57 0.7× 141 2.0× 31 489
Liemin Zhou China 13 53 0.2× 191 0.6× 254 2.7× 21 0.2× 264 3.8× 49 667

Countries citing papers authored by Sarah Soden

Since Specialization
Citations

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

Fields of papers citing papers by Sarah Soden

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Soden

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah Soden. A scholar is included among the top collaborators of Sarah Soden 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 Sarah Soden. Sarah Soden 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.
Sandritter, Tracy, et al.. (2023). Pharmacogenetic Testing in Patients with Autism Spectrum Disorder Evaluated in a Precision Medicine Clinic. Journal of Developmental & Behavioral Pediatrics. 44(8). e505–e510.
2.
Berrios, Courtney, et al.. (2022). Parental Understanding and Attitudes Following Pharmacogenomic Testing for Pediatric Neuropsychiatric Patients. Pharmacogenomics. 23(6). 345–354. 1 indexed citations
3.
Leeder, J. Steven, Andrea Gaedigk, Vincent S. Staggs, et al.. (2022). A longitudinal study of cytochrome P450 2D6 (CYP2D6) activity during adolescence. Clinical and Translational Science. 15(10). 2514–2527. 4 indexed citations
4.
Thiffault, Isabelle, Andrea M. Atherton, Bryce A. Heese, et al.. (2020). Pathogenic variants in KPTN gene identified by clinical whole-genome sequencing. Molecular Case Studies. 6(3). a003970–a003970. 4 indexed citations
5.
Berrios, Courtney, et al.. (2019). Parents of newborns in the NICU enrolled in genome sequencing research: hopeful, but not naïve. Genetics in Medicine. 22(2). 416–422. 33 indexed citations
6.
Thiffault, Isabelle, Emily Farrow, Lee Zellmer, et al.. (2018). Clinical genome sequencing in an unbiased pediatric cohort. Genetics in Medicine. 21(2). 303–310. 31 indexed citations
7.
Grote, Lauren, Isabelle Thiffault, Emily Farrow, et al.. (2018). Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings. Neurogenetics. 19(3). 205–213. 6 indexed citations
8.
Thiffault, Isabelle, Britton Zuccarelli, Xuan Yuan, et al.. (2017). Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease. BMC Medical Genetics. 18(1). 124–124. 11 indexed citations
9.
Soden, Sarah, et al.. (2016). Clinical and Pharmacologic Considerations for Guanfacine Use in Very Young Children. Journal of Child and Adolescent Psychopharmacology. 26(6). 498–504. 3 indexed citations
10.
Mizumoto, Shuji, Laurie D. Smith, Howard M. Saal, et al.. (2016). Functional validation of novel compound heterozygous variants in B3GAT3 resulting in severe osteopenia and fractures: expanding the disease phenotype. BMC Medical Genetics. 17(1). 86–86. 16 indexed citations
11.
Twist, Greyson P, Andrea Gaedigk, Neil Miller, et al.. (2016). Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences. npj Genomic Medicine. 1(1). 15007–15007. 89 indexed citations
12.
Thiffault, Isabelle, David J. Speca, Daniel C. Austin, et al.. (2015). A novel epileptic encephalopathy mutation in KCNB1 disrupts Kv2.1 ion selectivity, expression, and localization. The Journal of General Physiology. 146(5). 399–410. 66 indexed citations
13.
Raje, Nikita, Sarah Soden, Douglas Swanson, et al.. (2014). Utility of Next Generation Sequencing in Clinical Primary Immunodeficiencies. Current Allergy and Asthma Reports. 14(10). 468–468. 22 indexed citations
14.
Dinwiddie, Darrell L., Sarah Soden, Carol Saunders, et al.. (2013). Molecular diagnosis of infantile onset inflammatory bowel disease by exome sequencing. Genomics. 102(5-6). 442–447. 28 indexed citations
15.
Dinwiddie, Darrell L., Sarah Soden, Carol Saunders, et al.. (2013). De novoframeshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies. BMC Medical Genomics. 6(1). 32–32. 38 indexed citations
16.
Dinwiddie, Darrell L., Laurie D. Smith, Neil Miller, et al.. (2013). Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome. Genomics. 102(3). 148–156. 58 indexed citations
17.
Soden, Sarah, et al.. (2012). Nutrition, Physical Activity, and Bone Mineral Density in Youth With Autistic Spectrum Disorders. Journal of Developmental & Behavioral Pediatrics. 33(8). 618–624. 25 indexed citations
18.
Kingsmore, Stephen F., John D. Lantos, Darrell L. Dinwiddie, et al.. (2012). Next-generation community genetics for low- and middle-income countries. Genome Medicine. 4(3). 25–25. 53 indexed citations
19.
Abdelmoity, Ahmed, et al.. (2012). 15q11.2 Proximal Imbalances Associated With a Diverse Array of Neuropsychiatric Disorders and Mild Dysmorphic Features. Journal of Developmental & Behavioral Pediatrics. 33(7). 570–576. 30 indexed citations
20.
Soden, Sarah, et al.. (2007). 24-Hour Provoked Urine Excretion Test for Heavy Metals in Children with Autism and Typically Developing Controls, a Pilot Study. Clinical Toxicology. 45(5). 476–481. 46 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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