Louise K. Hoeffding

415 total citations
12 papers, 142 citations indexed

About

Louise K. Hoeffding is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Louise K. Hoeffding has authored 12 papers receiving a total of 142 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Psychiatry and Mental health. Recurrent topics in Louise K. Hoeffding's work include Genomic variations and chromosomal abnormalities (6 papers), Attention Deficit Hyperactivity Disorder (3 papers) and Congenital heart defects research (3 papers). Louise K. Hoeffding is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Attention Deficit Hyperactivity Disorder (3 papers) and Congenital heart defects research (3 papers). Louise K. Hoeffding collaborates with scholars based in Denmark, Germany and Iceland. Louise K. Hoeffding's co-authors include Thomas Werge, Preben Bo Mortensen, Line Olsen, Carsten Bøcker Pedersen, Betina B. Trabjerg, Anders Vangkilde, Thomas Sparsø, Wiktor Mazin, Thomas Folkmann Hansen and Henrik Ullum and has published in prestigious journals such as Schizophrenia Bulletin, JAMA Psychiatry and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.

In The Last Decade

Louise K. Hoeffding

12 papers receiving 139 citations

Peers

Countries citing papers authored by Louise K. Hoeffding

Since Specialization

Citations

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

Fields of papers citing papers by Louise K. Hoeffding

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louise K. Hoeffding

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

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Symptoms of ADHD are highly common in undiagnosed adults – A cross-sectional study in a large population of Danes 2018 ·Louise K. Hoeffding, Maria Haahr Nielsen, Janna Nissen, Maria Didriksen, Thomas Werge, (unknown), Christian Erikstrup, Ole Birger Pedersen, Henrik Hjalgrim, (unknown), Henrik Ullum, Kristoffer Sølvsten Burgdorf	4
2	Comorbidity of migraine with ADHD in adults 2018 ·BMC Neurology ·Thomas Folkmann Hansen, Louise K. Hoeffding, Lisette J. A. Kogelman, (unknown), Henrik Ullum, Erik Sørensen, Christian Erikstrup, Ole Birger Pedersen, Kaspar René Nielsen, Henrik Hjalgrim, Helene M. Paarup, Thomas Werge, Kristoffer Sølvsten Burgdorf	24
3	Socio-demographic characteristics of adults with self-reported ADHD symptoms in a Danish population of 12,415 blood donors 2018 ·Research at the University of Copenhagen (University of Copenhagen) ·Louise K. Hoeffding, Maria Haahr Nielsen, Maria Didriksen, (unknown), Thomas Werge, Kaspar René Nielsen, Christian Erikstrup, Ole Birger Pedersen, Henrik Hjalgrim, (unknown), Thomas Folkmann Hansen, Karina Banasik, Henrik Ullum, Kristoffer Sølvsten Burgdorf	3
4	A manual-based vocational rehabilitation program for patients with an acquired brain injury: study protocol of a pragmatic randomized controlled trial (RCT) 2017 ·Trials ·Louise K. Hoeffding, Maria Haahr Nielsen, Morten Arendt Rasmussen, Anne Norup, Juan Carlos Arango‐Lasprilla, (unknown), Kristoffer Sølvsten Burgdorf, (unknown), (unknown)	4
5	Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication 2017 ·JAMA Psychiatry ·Louise K. Hoeffding, Betina B. Trabjerg, Line Olsen, Wiktor Mazin, Thomas Sparsø, Anders Vangkilde, Preben Bo Mortensen, Carsten Bøcker Pedersen, Thomas Werge	64
6	Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total Danish Population—A Nationwide Register Study 2016 ·Schizophrenia Bulletin ·Anders Vangkilde, Line Olsen, Louise K. Hoeffding, Carsten Bøcker Pedersen, Preben Bo Mortensen, Thomas Werge, Betina B. Trabjerg	12
7	Evaluation of shared genetic susceptibility loci between autoimmune diseases and schizophrenia based on genome-wide association studies 2016 ·Nordic Journal of Psychiatry ·Louise K. Hoeffding, Anders Rosengren, Johan H. Thygesen, Henriette Schmock, Thomas Werge, Thomas Folkmann Hansen	8
8	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
9	Usefulness of the SNP microarray technology to identify rare mutations in the case of perinatal death 2015 ·Case Reports in Perinatal Medicine ·Louise K. Hoeffding, (unknown), (unknown), Thomas Folkmann Hansen, Thomas Werge	1
10	Identification of rare high-risk copy number variants affecting the dopamine transporter gene in mental disorders 2015 ·Nordic Journal of Psychiatry ·Louise K. Hoeffding, Linh T. Duong, Andrés Ingason, Anders Rosengren, (unknown), Stephanie H. Witt, Srdjan Djurovic, Ole A. Andreassen, Thomas Folkmann Hansen, Thomas Werge, Henrik B. Rasmussen	3
11	Sequence analysis of 17NRXN1deletions 2013 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Louise K. Hoeffding, Thomas Folkmann Hansen, Andrés Ingason, (unknown), Johan H. Thygesen, Rikke S. Møller, Niels Tommerup, George Kirov, Dan Rujescu, Lars Allan Larsen, Thomas Werge	9
12	Copy number variations in affective disorders and meta-analysis 2011 ·Psychiatric Genetics ·Line Olsen, Thomas Folkmann Hansen, Srdjan Djurovic, Eva Haastrup, (unknown), Louise K. Hoeffding, Anna Secher, Ómar Gústafsson, Klaus D. Jakobsen, Finn Cilius Nielsen, Henrik Ullum, Gunnar Morken, Ingrid Agartz, Ingrid Melle, Ulrik Gether, Ole A. Andreassen, Thomas Werge	3

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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