Karen Stals

2.5k total citations
31 papers, 938 citations indexed

About

Karen Stals is a scholar working on Molecular Biology, Surgery and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Karen Stals has authored 31 papers receiving a total of 938 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Surgery and 10 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Karen Stals's work include Pituitary Gland Disorders and Treatments (8 papers), Adrenal and Paraganglionic Tumors (6 papers) and Genomics and Rare Diseases (4 papers). Karen Stals is often cited by papers focused on Pituitary Gland Disorders and Treatments (8 papers), Adrenal and Paraganglionic Tumors (6 papers) and Genomics and Rare Diseases (4 papers). Karen Stals collaborates with scholars based in United Kingdom, United States and Canada. Karen Stals's co-authors include Sian Ellard, Andrew T. Hattersley, Ewan R. Pearson, Sylvia F. Boj, Anna Steele, Julian Hamilton‐Shield, Timothy Barrett, Jorge Ferrer, Márta Korbonits and Peter D. Turnpenny and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and The American Journal of Human Genetics.

In The Last Decade

Karen Stals

30 papers receiving 912 citations

Peers

Countries citing papers authored by Karen Stals

Since Specialization

Citations

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

Fields of papers citing papers by Karen Stals

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Stals

This figure shows the co-authorship network connecting the top 25 collaborators of Karen Stals. A scholar is included among the top collaborators of Karen Stals 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 Karen Stals. Karen Stals 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

#	Title	Journal	Authors	Indexed citations
1	Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay	American Journal of Medical Genetics Part A	Alanna Strong, Caoimhe McKenna et al.	1
2	COA5 has an essential role in the early stage of mitochondrial complex IV assembly	Life Science Alliance	Alfredo Cabrera‐Orefice, Geoffray Monteuuis et al.	0
3	Clinical and molecular characterization of novel FARS2 variants causing neonatal mitochondrial disease	Molecular Genetics and Metabolism	Wenqian Chen, Kyle Thompson et al.	2
4	Hereditary spastic paraparesis presenting as cerebral palsy due to ADD3 variant with mechanistic insight provided by a Drosophila γ‐adducin model	Clinical Genetics	Edgar Buhl, Bangfu Zhu et al.	4
5	Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome	The American Journal of Human Genetics	Sian Ellard, Karen Stals et al.	22
6	Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly	Genome Medicine	William L. Macken, Gabrielle Wheway et al.	23
7	Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome	SHILAP Revista de lepidopterología	Emma Wakeling, Meriel McEntagart et al.	11
8	Risk category system to identify pituitary adenoma patients with AIP mutations	Journal of Medical Genetics	Francisca Caimari, Laura C. Hernández‐Ramírez et al.	27
9	Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy	European Journal of Human Genetics	Karen Low, Karen Stals et al.	18
10	Homozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian disease	Genetics in Medicine	Matthew N. Wakeling, Thomas W. Laver et al.	23
11	An exome sequencing strategy to diagnose lethal autosomal recessive disorders	European Journal of Human Genetics	Sian Ellard, Emma Kivuva et al.	36
12	HNF1B deletions in patients with young‐onset diabetes but no known renal disease	Diabetic Medicine	Emma L. Edghill, Karen Stals et al.	32
13	Genetic analysis in a patient presenting with meningioma and familial isolated pituitary adenoma (FIPA) reveals selective involvement of the R81X mutation of the AIP gene in the pathogenesis of the pituitary tumor	Pituitary	Federica Guaraldi, Gary L. Gallia et al.	17
14	AIPMutation in Pituitary Adenomas in the 18th Century and Today	New England Journal of Medicine	Harvinder Chahal, Karen Stals et al.	94
15	JAG1 mutations are found in approximately one third of patients presenting with only one or two clinical features of Alagille syndrome	Clinical Genetics	Karen Stals, Martin Day et al.	50
16	AIP mutation in pituitary adenomas		Karen Stals, Giampaolo Trivellin et al.	9
17	Functional characterisation of aryl hydrocarbon receptor interacting protein (AIP) promoter and silent mutations		Harvinder Chahal, Peter King et al.	1
18	Characterization of aryl hydrocarbon receptor interacting protein (AIP) mutations in familial isolated pituitary adenoma families	Human Mutation	Susana Igreja, Peter King et al.	132
19	Hepatocyte nuclear factor-1 gene deletions--a common cause of renal disease	Nephrology Dialysis Transplantation	Emma L. Edghill, Richard A. Oram et al.	82
20	Macrosomia and Hyperinsulinaemic Hypoglycaemia in Patients with Heterozygous Mutations in the HNF4A Gene	PLoS Medicine	Ewan R. Pearson, Sylvia F. Boj et al.	299

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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