Laura L. Klitten

810 total citations
10 papers, 209 citations indexed

About

Laura L. Klitten is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Laura L. Klitten has authored 10 papers receiving a total of 209 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Laura L. Klitten's work include Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Chromosomal and Genetic Variations (2 papers). Laura L. Klitten is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Chromosomal and Genetic Variations (2 papers). Laura L. Klitten collaborates with scholars based in Denmark, United Kingdom and United States. Laura L. Klitten's co-authors include Niels Tommerup, Rikke S. Møller, Helle Hjalgrim, Steven L. Coon, Jong‐So Kim, Martin F. Rath, David C. Klein, Morten Møller, Thomas Werge and Linh T. Duong and has published in prestigious journals such as Epilepsia, Experimental Eye Research and Epilepsy Research.

In The Last Decade

Laura L. Klitten

9 papers receiving 208 citations

Peers

Countries citing papers authored by Laura L. Klitten

Since Specialization

Citations

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

Fields of papers citing papers by Laura L. Klitten

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laura L. Klitten. 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 Laura L. Klitten. The network helps show where Laura L. Klitten may publish in the future.

Co-authorship network of co-authors of Laura L. Klitten

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family 2015 ·European Journal of Medical Genetics ·Linh T. Duong, Louise K. Hoeffding, Kirsten Bruun Petersen, (unknown), Johan H. Thygesen, Laura L. Klitten, Niels Tommerup, Andrés Ingason, Thomas Werge	7
2	Dysregulation of FOXG1 by ring chromosome 14 2015 ·Molecular Cytogenetics ·(unknown), Laura L. Klitten, Mads Bak, Helle Hjalgrim, Rikke S. Møller, Niels Tommerup	7
3	Reduced ceramide synthase 2 activity causes progressive myoclonic epilepsy 2014 ·Annals of Clinical and Translational Neurology ·(unknown), Anne S. Olsen, Ditte Neess, Oshrit Ben‐David, Laura L. Klitten, Jan Larsen, Anne Sabers, John Vissing, Jørgen E. Nielsen, Lis Hasholt, Andrés D. Klein, Michael Tsoory, Helle Hjalgrim, Niels Tommerup, Anthony H. Futerman, Rikke S. Møller, Nils J. Færgeman	44
4	The role of SLC2A1 in early onset and childhood absence epilepsies 2013 ·Epilepsy Research ·Hiltrud Muhle, Ingo Helbig, Tobias Guldberg Frøslev, Arvid Suls, Sarah von Spiczak, Laura L. Klitten, Hans A. Dahl, Klaus Brusgaard, Bernd A. Neubauer, Peter De Jonghe, Niels Tommerup, Ulrich Stephani, Helle Hjalgrim, Rikke S. Møller	11
5	Atypical Vitamin B₆ Deficiency 2013 ·Journal of Child Neurology ·(unknown), Sarah von Spiczak, Nanda M. Verhoeven‐Duif, Rikke S. Møller, Rainer Boor, Hiltrud Muhle, Johanna Jähn, Laura L. Klitten, Helle Hjalgrim, Dick Lindhout, Ulrich Stephani, Marjan J. A. van Kempen, Ingo Helbig	13
6	Genetic studies in congenital anterior midline cervical cleft 2012 ·American Journal of Medical Genetics Part A ·Linda P. Jakobsen, Per Pfeiffer, Mette Klarskov Andersen, Hans Eiberg, Lars Hestbjerg Hansen, Yuan Mang, Mads Bak, Rikke S. Møller, Laura L. Klitten, Niels Tommerup	12
7	Mutations inNRXN1in a family multiply affected with brain disorders:NRXN1mutations and brain disorders 2012 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Linh T. Duong, Laura L. Klitten, Rikke S. Møller, Andrés Ingason, Klaus D. Jakobsen, (unknown), Michael Didriksen, Helle Hjalgrim, Thomas Werge, Niels Tommerup	48
8	A balanced translocation disruptsSYNGAP1in a patient with intellectual disability, speech impairment, and epilepsy with myoclonic absences (EMA) 2011 ·Epilepsia ·Laura L. Klitten, Rikke S. Møller, Marina Nikanorova, Asli Silahtaroglu, Helle Hjalgrim, Niels Tommerup	21
9	9q subtelomeric deletion syndrome with diaphragmatic hernia 2009 ·American Journal of Medical Genetics Part A ·Laura L. Klitten, Niels Tommerup, Helle Hjalgrim, Rikke S. Møller	0
10	Localization and regulation of dopamine receptor D4 expression in the adult and developing rat retina 2008 ·Experimental Eye Research ·Laura L. Klitten, Martin F. Rath, Steven L. Coon, Jong‐So Kim, David C. Klein, Morten Møller	46

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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