Soo‐Mi Park

6.5k total citations
39 papers, 794 citations indexed

About

Soo‐Mi Park is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Soo‐Mi Park has authored 39 papers receiving a total of 794 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 15 papers in Genetics and 7 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Soo‐Mi Park's work include Genetic Syndromes and Imprinting (5 papers), Genomics and Rare Diseases (5 papers) and Congenital heart defects research (4 papers). Soo‐Mi Park is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Genomics and Rare Diseases (5 papers) and Congenital heart defects research (4 papers). Soo‐Mi Park collaborates with scholars based in United Kingdom, Netherlands and Australia. Soo‐Mi Park's co-authors include Eamonn R. Maher, Ruth Casey, David Fitzpatrick, Nadia Schoenmakers, Benjamin Challis, Helen V. Firth, Carla Moran, Pradeep Vasudevan, Meredith Wilson and Olivera Spasić-Bošković and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Annals of Neurology.

In The Last Decade

Soo‐Mi Park

37 papers receiving 775 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Soo‐Mi Park United Kingdom	15	464	258	147	79	74	39	794
Erik-Jan Kamsteeg Netherlands	15	425 0.9×	320 1.2×	60 0.4×	84 1.1×	65 0.9×	21	874
Davide Tonduti Italy	19	728 1.6×	183 0.7×	127 0.9×	35 0.4×	27 0.4×	64	1.1k
Sahar Mansour United Kingdom	11	575 1.2×	288 1.1×	39 0.3×	47 0.6×	81 1.1×	15	854
Maria Teresa Pirro Italy	9	555 1.2×	193 0.7×	260 1.8×	30 0.4×	65 0.9×	9	805
Ruen Yao China	15	385 0.8×	334 1.3×	55 0.4×	61 0.8×	44 0.6×	64	657
Meena Balasubramanian United Kingdom	18	310 0.7×	555 2.2×	45 0.3×	50 0.6×	79 1.1×	74	802
Catherine Vaurs‐Barrière France	15	324 0.7×	172 0.7×	147 1.0×	60 0.8×	25 0.3×	26	734
Michael H. Guo United States	20	603 1.3×	509 2.0×	174 1.2×	74 0.9×	70 0.9×	33	1.2k
Marcello Niceta Italy	18	489 1.1×	304 1.2×	24 0.2×	35 0.4×	60 0.8×	53	810
Makiko Meguro‐Horike Japan	14	477 1.0×	268 1.0×	111 0.8×	88 1.1×	57 0.8×	35	829

Countries citing papers authored by Soo‐Mi Park

Since Specialization

Citations

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

Fields of papers citing papers by Soo‐Mi Park

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Soo‐Mi Park. 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 Soo‐Mi Park. The network helps show where Soo‐Mi Park may publish in the future.

Co-authorship network of co-authors of Soo‐Mi Park

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

All Works

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20 of 20 papers shown

French, Courtney E., Helen Dolling, Karyn Mégy, et al.. (2022). Refinements and considerations for trio whole-genome sequence analysis when investigating Mendelian diseases presenting in early childhood. Human Genetics and Genomics Advances. 3(3). 100113–100113. 10 indexed citations

Brown, Richard S., Hannah M. Grayton, John H. Livingston, et al.. (2020). Clinical and radiological characterization of novel FIG4 ‐related combined system disease with neuropathy. Clinical Genetics. 98(2). 147–154. 13 indexed citations

Hikmat, Mondy, et al.. (2020). Normosmic idiopathic hypogonadotropic hypogonadism due to a novel GNRH1 variant in two siblings. Endocrinology Diabetes and Metabolism Case Reports. 2020. 9 indexed citations

Hague, Jennifer, et al.. (2019). Clinical Diagnosis of Classical Cornelia de Lange Syndrome Made From Postmortem Examination of Second Trimester Fetus With Novel NIPBL Pathogenic Variant. Pediatric and Developmental Pathology. 22(5). 475–479. 9 indexed citations

MacFarlane, James, et al.. (2019). A case of Birt-Hogg-Dube syndrome presenting with a rare oncocytic non-secretory phaeochromocytoma. Endocrine Abstracts. 1 indexed citations

Casey, Ruth, et al.. (2019). Identification of novel pathogenic variants and features in patients with pseudohypoparathyroidism and acrodysostosis, subtypes of the newly classified inactivating PTH/PTHrP signaling disorders. American Journal of Medical Genetics Part A. 179(7). 1330–1337.

Ansari, Morad, Hemant Bengani, Graeme R. Grimes, et al.. (2018). BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange–like syndrome. Nature Genetics. 50(3). 329–332. 89 indexed citations

Andrews, Katrina, Benjamin Challis, Soo‐Mi Park, et al.. (2018). Clinical Practice Guidance: Surveillance for phaeochromocytoma and paraganglioma in paediatric succinate dehydrogenase gene mutation carriers. Clinical Endocrinology. 90(4). 499–505. 20 indexed citations

Schon, Katherine, Olivera Spasić-Bošković, Kim Brügger, et al.. (2017). Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected child. Neurogenetics. 18(1). 49–55. 6 indexed citations

10.

Hague, Jennifer, Isabelle Delon, Kim Brügger, et al.. (2016). Molecularly proven mosaicism in phenotypically normal parent of a girl with Freeman–Sheldon Syndrome caused by a pathogenic MYH3 mutation. American Journal of Medical Genetics Part A. 170(6). 1608–1612. 9 indexed citations

11.

Parker, Michael, Alan Fryer, Deborah Shears, et al.. (2015). De novo, heterozygous, loss‐of‐function mutations in SYNGAP1 cause a syndromic form of intellectual disability. American Journal of Medical Genetics Part A. 167(10). 2231–2237. 79 indexed citations

12.

Lax, Nichola Z., Charlotte L. Alston, Katherine Schon, et al.. (2015). Neuropathologic Characterization of Pontocerebellar Hypoplasia Type 6 Associated With Cardiomyopathy and Hydrops Fetalis and Severe Multisystem Respiratory Chain Deficiency due to NovelRARS2Mutations. Journal of Neuropathology & Experimental Neurology. 74(7). 688–703. 25 indexed citations

13.

Grozeva, Detelina, Keren Carss, Olivera Spasić-Bošković, et al.. (2014). De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability. The American Journal of Human Genetics. 94(4). 618–624. 89 indexed citations

14.

McKie, Arthur B., Julie Vogt, Kyra E. Stuurman, et al.. (2014). Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndrome. Acta Neuropathologica Communications. 2(1). 148–148. 18 indexed citations

15.

Schoenmakers, Nadia, Hakan Cangül, Adeline K. Nicholas, et al.. (2013). A comprehensive next generation sequencing-based strategy for genetic diagnosis in congenital hypothyroidism. 33. 8 indexed citations

16.

Moran, Carla, Nadia Schoenmakers, Maura Agostini, et al.. (2013). An Adult Female With Resistance to Thyroid Hormone Mediated by Defective Thyroid Hormone Receptor α. The Journal of Clinical Endocrinology & Metabolism. 98(11). 4254–4261. 97 indexed citations

17.

Burkitt‐Wright, Emma, Lisa Bradley, Vivienne McConnell, et al.. (2012). Neonatal lethal Costello syndrome and unusual dinucleotide deletion/insertion mutations in HRAS predicting p.Gly12Val. American Journal of Medical Genetics Part A. 158A(5). 1102–1110. 18 indexed citations

18.

Park, Soo‐Mi, et al.. (2010). Physicochemical characteristics, antimicrobial activity, ACE inhibitory activity of chitosan-salt, and its antihypertensive effect. Food Science and Biotechnology. 19(3). 777–784. 2 indexed citations

19.

Coccia, Margherita, Simon P. Brooks, Tom R. Webb, et al.. (2009). X-linked cataract and Nance-Horan syndrome are allelic disorders. Human Molecular Genetics. 18(14). 2643–2655. 50 indexed citations

20.

Park, Soo‐Mi, Christine M Hall, R. F. Gray, & Helen V. Firth. (2007). Persistent upper airway obstruction is a diagnostic feature of spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type) with further evidence for dominant inheritance. American Journal of Medical Genetics Part A. 143A(17). 2024–2028. 4 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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