Soo‐Mi Park

6.5k citations

39 papers · 794 · h-index 15

Impact in

Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Endocrinology, Diabetes and Metabolism top 10%
- Thyroid Disorders and Treatments
- Growth Hormone and Insulin-like Growth Factors

Papers in

Molecular Biology 16
- Congenital heart defects research 4
Genetics 15
- Genetic Syndromes and Imprinting 5
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 4

Co-authors: Eamonn R. Maher (9 shared papers)Ruth Casey (9 shared papers)David Fitzpatrick (2 shared papers)Nadia Schoenmakers (5 shared papers)Benjamin Challis (4 shared papers)Helen V. Firth (3 shared papers)Carla Moran (2 shared papers)Meredith Wilson (2 shared papers)
Journals: Clinical Endocrinology (5 papers)Acta Neuropathologica Communications (2 papers)Nature Genetics (1 paper)Human Genetics and Genomics Advances (1 paper)Human Molecular Genetics (1 paper)
Partner nations: United Kingdom Netherlands Australia

In The Last Decade

Soo‐Mi Park

37 papers receiving 775 citations

Peers

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-authors

The 25 scholars most cited alongside Soo‐Mi Park, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Soo‐Mi Park Line = papers co-authored together Soo‐Mi Park links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 39 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	An Adult Female With Resistance to Thyroid Hormone Mediated by Defective Thyroid Hormone Receptor α The Journal of Clinical Endocrinology & Metabolism ·Carla Moran, Nadia Schoenmakers, Maura Agostini, Erik Schoenmakers, Amaka C Offiah, A. Kydd, G. Kahaly, Susan Mohr-Kahaly, Odelia Rajanayagam, Greta Lyons, Nicholas J. Wareham, David Halsall, Mehul Dattani, Stephen G. Hughes, Mark Gurnell, Soo‐Mi Park, Krishna Chatterjee	2013	97
2	BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange–like syndrome Nature Genetics ·(unknown), Gabrielle Olley, Morad Ansari, Hemant Bengani, Graeme R. Grimes, James Rhodes, Alex von Kriegsheim, Ana Blatnik, Fiona J. Stewart, Emma Wakeling, Nicola Carroll, Alison Ross, Soo‐Mi Park, Wendy A. Bickmore, Madapura M. Pradeepa, David Fitzpatrick	2018	89
3	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 ·Detelina Grozeva, Keren Carss, Olivera Spasić-Bošković, Michael Parker, Hayley Archer, Helen V. Firth, Soo‐Mi Park, Natalie Canham, Susan Holder, Meredith Wilson, Anna Hackett, Michael Field, James Floyd, Matthew E. Hurles, F. Lucy Raymond	2014	89
4	De novo, heterozygous, loss‐of‐function mutations in SYNGAP1 cause a syndromic form of intellectual disability American Journal of Medical Genetics Part A ·Michael Parker, Alan Fryer, Deborah Shears, Katherine Lachlan, Shane McKee, Alex Magee, Shehla Mohammed, Pradeep Vasudevan, Soo‐Mi Park, Valérie Benoît, Damien Lederer, Isabelle Maystadt, DDD Study, David Fitzpatrick	2015	79
5	Pathogenic Mitochondrial t RNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease Human Mutation ·Emma L. Blakely, John W. Yarham, Charlotte L. Alston, Kate Craig, Joanna Poulton, Charlotte Brierley, Soo‐Mi Park, Andrew Dean, John H. Xuereb, Kirstie N. Anderson, Alistair Compston, Chris Allen, Saba Sharif, Peter Enevoldson, Martin Wilson, Simon Hammans, Douglass M. Turnbull, Robert McFarland, Robert W. Taylor	2013	61
6	X-linked cataract and Nance-Horan syndrome are allelic disorders Human Molecular Genetics ·Margherita Coccia, Simon P. Brooks, Tom R. Webb, Katja Christodoulou, Izabella O. Wozniak, Victoria Murday, Martha Balicki, Harris A. Yee, Teresia Wangensteen, Ruth Riise, Anand Saggar, Soo‐Mi Park, Naheed Kanuga, Peter J. Francis, Eamonn R. Maher, Anthony T. Moore, Isabelle Russell‐Eggitt, Alison J. Hardcastle	2009	50
7	A review of the tumour spectrum of germline succinate dehydrogenase gene mutations: Beyond phaeochromocytoma and paraganglioma Clinical Endocrinology ·James MacFarlane, Keat Cheah Seong, Chad Bisambar, Basetti Madhu, Kieren Allinson, Alison Marker, Anne Y. Warren, Soo‐Mi Park, Olivier Giger, Benjamin Challis, Eamonn R. Maher, Ruth Casey	2020	39
8	Translating In Vivo Metabolomic Analysis of Succinate Dehydrogenase–Deficient Tumors Into Clinical Utility JCO Precision Oncology ·Ruth Casey, Mary A. McLean, Basetti Madhu, Benjamin Challis, Rogier ten Hoopen, Thomas M. Roberts, Graeme R. Clark, Deborah Pitfield, Helen Simpson, V.R. Bulusu, Kieren Allinson, Lisa Happerfield, Soo‐Mi Park, Alison Marker, Olivier Giger, Eamonn R. Maher, Ferdia A. Gallagher	2018	29
9	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 ·Nichola Z. Lax, Charlotte L. Alston, Katherine Schon, Soo‐Mi Park, Deepa Krishnakumar, Langping He, Gavin Falkous, Amanda Ogilvy‐Stuart, C. Lees, R. H. M. King, Iain P. Hargreaves, Garry K. Brown, Robert McFarland, Andrew Dean, Robert W. Taylor	2015	25
10	Genetic testing for hereditary hyperparathyroidism and familial hypocalciuric hypercalcaemia in a large UK cohort Clinical Endocrinology ·Sashi Mariathasan, Katrina Andrews, Edward H. Thompson, Ben Challis, Sarah Wilcox, Heather Pierce, Julia Hale, Sarah L Spiden, Gavin Fuller, Helen Simpson, Brian Fish, Piyush Jani, Ian Seetho, Ruth Armstrong, Louise Izatt, Mamta Joshi, Anand Velusamy, Soo‐Mi Park, Ruth Casey	2020	25
11	Clinical Practice Guidance: Surveillance for phaeochromocytoma and paraganglioma in paediatric succinate dehydrogenase gene mutation carriers Clinical Endocrinology ·Mei Yin Wong, Katrina Andrews, Benjamin Challis, Soo‐Mi Park, Carlo L. Acerini, Eamonn R. Maher, Ruth Casey	2018	20
12	Management of primary hyperparathyroidism in pregnancy: a case series Endocrinology Diabetes and Metabolism Case Reports ·Aisling McCarthy, Sophie Howarth, Serena Khoo, Julia Hale, Sue Oddy, David Halsall, Brian Fish, Sashi Mariathasan, Katrina Andrews, Samson O Oyibo, Manjula Samyraju, Katarzyna Gajewska‐Knapik, Soo‐Mi Park, Diana Wood, Carla Moran, Ruth Casey	2019	20
13	Neonatal lethal Costello syndrome and unusual dinucleotide deletion/insertion mutations in HRAS predicting p.Gly12Val American Journal of Medical Genetics Part A ·Emma Burkitt‐Wright, Lisa Bradley, Jennifer Shorto, Vivienne McConnell, Caroline Gannon, Helen V. Firth, Soo‐Mi Park, Angela D’Amore, Paul Munyard, Peter D. Turnpenny, Amanda Charlton, Meredith Wilson, Bronwyn Kerr	2012	18
14	Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndrome Acta Neuropathologica Communications ·Arthur B. McKie, Atif Alsaedi, Julie Vogt, Kyra E. Stuurman, Marjan M. Weiss, Hassan Shakeel, Louise Tee, Neil V. Morgan, Peter G. J. Nikkels, Gijs van Haaften, Soo‐Mi Park, Jasper J. van der Smagt, Marianna Bugiani, Eamonn R. Maher	2014	18
15	Haploinsufficiency of CUX1 Causes Nonsyndromic Global Developmental Delay With Possible Catch‐up Development Annals of Neurology ·Konrad Platzer, Benjamin Cogné, Jennifer Hague, Carlo Marcelis, Diana Mitter, Katrin Oberndorff, Soo‐Mi Park, Hans Kristian Ploos van Amstel, Ingrid Simonic, Jasper J. van der Smagt, Alexander P.A. Stegmann, Servi J.C. Stevens, Constance T. R. M. Stumpel, Marie Vincent, Johannes R. Lemke, Rami Abou Jamra	2018	16
16	Clinical and radiological characterization of novel FIG4 ‐related combined system disease with neuropathy Clinical Genetics ·Georgia Wright, Richard S. Brown, Hannah M. Grayton, John H. Livingston, Soo‐Mi Park, Alasdair Parker, Anjla Patel, Ingrid Simonic, Adam G. Thomas, Gayatri Vadlamani, Rita Horváth, Pooja Harijan	2020	13
17	Intrauterine death following intraamniotic triiodothyronine and thyroxine therapy for fetal goitrous hypothyroidism associated with polyhydramnios and caused by a thyroglobulin mutation Endocrinology Diabetes and Metabolism Case Reports ·Pradeep Vasudevan, Corrina Powell, Adeline K. Nicholas, Ian Scudamore, James Greening, Soo‐Mi Park, Nadia Schoenmakers	2017	11
18	Refinements and considerations for trio whole-genome sequence analysis when investigating Mendelian diseases presenting in early childhood Human Genetics and Genomics Advances ·Courtney E. French, Helen Dolling, Karyn Mégy, Alba Sanchis-Juan, Ajay Kumar, Isabelle Delon, Matthew N. Wakeling, Lucy Mallin, Shruti Agrawal, Topun Austin, Florence Walston, Soo‐Mi Park, Alasdair Parker, Chinthika Piyasena, Kimberley Bradbury, Sian Ellard, David H. Rowitch, F. Lucy Raymond	2022	10
19	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 ·Jennifer Hague, Isabelle Delon, Kim Brügger, Howard Martin, Stephen Abbs, Soo‐Mi Park	2016	9
20	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 ·Jennifer Hague, Philip Twiss, Zoe Mead, Soo‐Mi Park	2019	9

About Soo‐Mi Park

Soo‐Mi Park is a scholar working on Molecular Biology, Genetics, Endocrinology, Diabetes and Metabolism, Pulmonary and Respiratory Medicine and Surgery, having authored 39 papers that have together received 794 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (5 papers), Genomics and Rare Diseases (5 papers), Congenital heart defects research (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Thyroid Disorders and Treatments (4 papers), Parathyroid Disorders and Treatments (4 papers), Cancer, Hypoxia, and Metabolism (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Genetics (258 citations), Endocrinology, Diabetes and Metabolism (147 citations), Clinical Biochemistry (51 citations), Molecular Biology (464 citations) and Nephrology (42 citations). Soo‐Mi Park has collaborated with scholars based in United Kingdom, Netherlands and Australia. Frequent co-authors include Eamonn R. Maher, Ruth Casey, David Fitzpatrick, Nadia Schoenmakers, Benjamin Challis, Helen V. Firth, Carla Moran, Meredith Wilson, David Halsall and Olivera Spasić-Bošković. Their work appears in journals such as Clinical Endocrinology, Acta Neuropathologica Communications, Nature Genetics, Human Genetics and Genomics Advances and Human Molecular Genetics.

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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