K Lillquist

697 total citations
14 papers, 523 citations indexed

About

K Lillquist is a scholar working on Molecular Biology, Nephrology and Oncology. According to data from OpenAlex, K Lillquist has authored 14 papers receiving a total of 523 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Nephrology and 3 papers in Oncology. Recurrent topics in K Lillquist's work include Bone health and treatments (3 papers), Parathyroid Disorders and Treatments (3 papers) and Congenital heart defects research (2 papers). K Lillquist is often cited by papers focused on Bone health and treatments (3 papers), Parathyroid Disorders and Treatments (3 papers) and Congenital heart defects research (2 papers). K Lillquist collaborates with scholars based in Denmark, Australia and Poland. K Lillquist's co-authors include Maninder Kaur, Ian D. Krantz, Bart Loeys, Meredith Wilson, Antonio Musio, Dale Dorsett, Feliciano J. Ramos, Sergey Korolev, Antonie D. Kline and Victoria Mok Siu and has published in prestigious journals such as The American Journal of Human Genetics, Heart and Acta Paediatrica.

In The Last Decade

K Lillquist

13 papers receiving 510 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
K Lillquist Denmark 8 381 212 51 36 35 14 523
Carole Brewer United Kingdom 8 191 0.5× 301 1.4× 55 1.1× 49 1.4× 11 0.3× 9 484
R Elles United Kingdom 11 318 0.8× 302 1.4× 78 1.5× 75 2.1× 8 0.2× 21 530
Marion Gérard‐Blanluet France 13 200 0.5× 158 0.7× 14 0.3× 72 2.0× 10 0.3× 24 399
Benedetta Toschi Italy 11 117 0.3× 145 0.7× 21 0.4× 26 0.7× 46 1.3× 28 309
Koen Devriendt Belgium 9 205 0.5× 137 0.6× 20 0.4× 61 1.7× 6 0.2× 13 290
Claire Turner United Kingdom 13 304 0.8× 414 2.0× 31 0.6× 183 5.1× 24 0.7× 14 578
Sandra Corbani Lebanon 10 225 0.6× 163 0.8× 13 0.3× 22 0.6× 11 0.3× 23 387
Maria Accadia Italy 14 136 0.4× 116 0.5× 12 0.2× 19 0.5× 20 0.6× 34 421
Laurence Perrin France 10 141 0.4× 149 0.7× 14 0.3× 29 0.8× 8 0.2× 28 366
Giorgio Filippi Italy 14 304 0.8× 281 1.3× 29 0.6× 80 2.2× 2 0.1× 27 581

Countries citing papers authored by K Lillquist

Since Specialization
Citations

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

Fields of papers citing papers by K Lillquist

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K Lillquist

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

All Works

14 of 14 papers shown
1.
Deardorff, Matthew A., Maninder Kaur, Dinah Yaeger, et al.. (2007). Mutations in Cohesin Complex Members SMC3 and SMC1A Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation. The American Journal of Human Genetics. 80(3). 485–494. 385 indexed citations
2.
Lindquist, Suzanne Granhøj, Claes Lundsteen, William C. Pedersen, et al.. (2005). Further delineation of the 22q13 deletion syndrome. Clinical Dysmorphology. 14(2). 55–60. 36 indexed citations
3.
Schwarz, Peter, et al.. (2000). Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism associated with mutations in the human Ca2+-sensing receptor gene in three Danish families. Scandinavian Journal of Clinical and Laboratory Investigation. 60(3). 221–228. 18 indexed citations
4.
Lillquist, K, et al.. (1989). Effect of folic acid supplementation on small-for-gestational-age infants born at term. European Journal of Pediatrics. 149(1). 65–67. 7 indexed citations
5.
Ford, J. H., et al.. (1988). Unusual segregation in a family with a 11/21 translocation. Clinical Genetics. 33(6). 449–453. 2 indexed citations
6.
Lillquist, K, et al.. (1988). [Occurrence and types of juvenile rheumatoid arthritis in the County of Jutland 1970-1977 and 1978-1986].. PubMed. 150(6). 342–6. 3 indexed citations
7.
Høst, Arne, Susanne Halken, J Kamper, & K Lillquist. (1988). Prostaglandin E1 treatment in ductus dependent congenital cardiac malformation. A review of the treatment of 34 neonates.. PubMed. 35(1). 81–4. 13 indexed citations
8.
Lillquist, K, et al.. (1985). [Familial hypocalciuric hypercalcemia].. PubMed. 147(39). 3054–6. 1 indexed citations
9.
Lillquist, K, et al.. (1983). PRIMARY HYPERPARATHYROIDISM IN INFANCY ASSOCIATED WITH FAMILIAL HYPOCALCIURIC HYPERCALCEMIA. Acta Paediatrica. 72(4). 625–629. 15 indexed citations
10.
Brinkløv, M. M., et al.. (1980). Urinary Loss of Oxypurines in Hypoxic Premature Neonates. Neonatology. 38(1-2). 40–48. 14 indexed citations
11.
Lillquist, K, Jens Haase, & Per Thayssen. (1979). Operative treatment of cerebral arteriovenous aneurysm of vein of Galen complicated by congestive heart failure.. Heart. 42(6). 738–741. 4 indexed citations
12.
Rasmussen, Knud, et al.. (1979). [Evaluation of heart function in patients with acute myocardial infarction using apex cardiography].. PubMed. 141(45). 3094–6.
13.
Lillquist, K, et al.. (1978). THE ABSENCE OF FACTOR II IN A CHILD WITH SYSTEMIC LUPUS ERYTHEMATOSUS. Acta Paediatrica. 67(4). 533–536. 21 indexed citations
14.
Lillquist, K, et al.. (1976). SPONTANEOUS CEREBRAL THROMBOSIS IN CHILDREN Report of Two Cases. Acta Paediatrica. 65(1). 119–124. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Carole Brewer Breakdown of academic impact, for papers by R Elles Breakdown of academic impact, for papers by Marion Gérard‐Blanluet Breakdown of academic impact, for papers by Benedetta Toschi Breakdown of academic impact, for papers by Koen Devriendt Breakdown of academic impact, for papers by Claire Turner Breakdown of academic impact, for papers by Sandra Corbani Breakdown of academic impact, for papers by Maria Accadia Breakdown of academic impact, for papers by Laurence Perrin Breakdown of academic impact, for papers by Giorgio Filippi
Rankless by CCL
2026