Millie Young

508 total citations
11 papers, 223 citations indexed

About

Millie Young is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Millie Young has authored 11 papers receiving a total of 223 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Surgery. Recurrent topics in Millie Young's work include Neurogenetic and Muscular Disorders Research (4 papers), Congenital Anomalies and Fetal Surgery (3 papers) and RNA modifications and cancer (2 papers). Millie Young is often cited by papers focused on Neurogenetic and Muscular Disorders Research (4 papers), Congenital Anomalies and Fetal Surgery (3 papers) and RNA modifications and cancer (2 papers). Millie Young collaborates with scholars based in United States. Millie Young's co-authors include Kevin A. Strauss, Karlla W. Brigatti, Erik G. Puffenberger, Christine Hendrickson, Freeman Miller, Michael D. Fox, Robert M. Reed, Vincent J. Carson, William G. Mackenzie and Katie B. Williams and has published in prestigious journals such as PLoS ONE, Hepatology and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Millie Young

11 papers receiving 221 citations

Peers

Millie Young

GENET

SURGE

Patricia Galvin‐Parton United States

Leigh B. Waddell Australia

Mohammad Al-Owain Saudi Arabia

Ewa Goljan Saudi Arabia

Joanna Taybert Poland

Ilona Visapää Finland

Fengxia Yao China

Silvio Ferraris Italy

Ahmad Alodaib Saudi Arabia

Dennis W. Bartholomew United States

Patricia Galvin‐Parton United States

Millie Young

192 ×1.4

19 ×0.3

GENET

84 ×1.5

GENET

24 ×0.5

SURGE

93 ×2.7

Citations per year, relative to Millie Young Millie Young (= 1×) peers Patricia Galvin‐Parton

Countries citing papers authored by Millie Young

Since Specialization

Citations

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

Fields of papers citing papers by Millie Young

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Millie Young

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

All Works

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11 of 11 papers shown

Brigatti, Karlla W., et al.. (2024). Preemptive dual therapy for children at risk for infantile‐onset spinal muscular atrophy. Annals of Clinical and Translational Neurology. 11(7). 1868–1878. 2 indexed citations

Williams, Katie B., Michael Horst, Millie Young, et al.. (2022). Clinical characterization of familial hypercholesterolemia due to an amish founder mutation in Apolipoprotein B. BMC Cardiovascular Disorders. 22(1). 109–109. 4 indexed citations

Young, Millie, Karlla W. Brigatti, Robert M. Reed, et al.. (2021). Nusinersen by subcutaneous intrathecal catheter for symptomatic spinal muscular atrophy patients with complex spine anatomy. Muscle & Nerve. 65(1). 51–59. 12 indexed citations

Strauss, Kevin A., Katie B. Williams, Millie Young, et al.. (2020). Glutaric acidemia type 1: Treatment and outcome of 168 patients over three decades. Molecular Genetics and Metabolism. 131(3). 325–340. 30 indexed citations

Young, Millie, Olivia Wenger, Karlla W. Brigatti, et al.. (2019). Recessive GM3 synthase deficiency: Natural history, biochemistry, and therapeutic frontier. Molecular Genetics and Metabolism. 126(4). 475–488. 36 indexed citations

Strauss, Kevin A., Charles E. Ahlfors, Kyle Soltys, et al.. (2019). Crigler‐Najjar Syndrome Type 1: Pathophysiology, Natural History, and Therapeutic Frontier. Hepatology. 71(6). 1923–1939. 27 indexed citations

Puffenberger, Erik G., et al.. (2018). Spinal muscular atrophy within Amish and Mennonite populations: Ancestral haplotypes and natural history. PLoS ONE. 13(9). e0202104–e0202104. 7 indexed citations

Strauss, Kevin A., Karlla W. Brigatti, Millie Young, et al.. (2018). Preliminary Safety and Tolerability of a Novel Subcutaneous Intrathecal Catheter System for Repeated Outpatient Dosing of Nusinersen to Children and Adults With Spinal Muscular Atrophy. Journal of Pediatric Orthopaedics. 38(10). e610–e617. 42 indexed citations

Strauss, Kevin A., Claudia Gonzaga‐Jauregui, Karlla W. Brigatti, et al.. (2017). Genomic diagnostics within a medically underserved population: efficacy and implications. Genetics in Medicine. 20(1). 31–41. 36 indexed citations

10.

Chowdhury, Devyani, Katie B. Williams, Aaron Chidekel, et al.. (2017). Management of Congenital Heart Disease Associated with Ellis-van Creveld Short-rib Thoracic Dysplasia. The Journal of Pediatrics. 191. 145–151. 6 indexed citations

11.

Benkert, Abigail R., et al.. (2015). Severe Salt-Losing 3β-Hydroxysteroid Dehydrogenase Deficiency: Treatment and Outcomes ofHSD3B2c.35G>A Homozygotes. The Journal of Clinical Endocrinology & Metabolism. 100(8). E1105–E1115. 21 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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