David M. Hougaard

61.7k total citations
289 papers, 9.4k citations indexed

About

David M. Hougaard is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, David M. Hougaard has authored 289 papers receiving a total of 9.4k indexed citations (citations by other indexed papers that have themselves been cited), including 87 papers in Molecular Biology, 83 papers in Genetics and 50 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in David M. Hougaard's work include Genetic Associations and Epidemiology (30 papers), Autism Spectrum Disorder Research (22 papers) and Neonatal Respiratory Health Research (19 papers). David M. Hougaard is often cited by papers focused on Genetic Associations and Epidemiology (30 papers), Autism Spectrum Disorder Research (22 papers) and Neonatal Respiratory Health Research (19 papers). David M. Hougaard collaborates with scholars based in Denmark, United States and Sweden. David M. Hougaard's co-authors include Bent Nørgaard‐Pedersen, Preben Bo Mortensen, Kristin Skogstrand, Poul Thorsen, Arieh S. Cohen, Anders D. Børglum, Jakob Grove, Ole Mors, B Nørgaard‐Pedersen and Lars Larsson and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Nature Genetics.

In The Last Decade

David M. Hougaard

285 papers receiving 9.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David M. Hougaard Denmark	52	2.1k	1.9k	1.4k	1.2k	1.1k	289	9.4k
John S. Adams United States	65	2.3k 1.1×	2.0k 1.1×	859 0.6×	1.2k 1.0×	1.5k 1.4×	210	14.8k
Robert Vlietinck Belgium	58	1.7k 0.8×	3.0k 1.6×	2.0k 1.5×	1.2k 0.9×	1.2k 1.1×	260	10.3k
Susan M. Ring United Kingdom	49	2.9k 1.4×	2.4k 1.3×	3.4k 2.5×	1.6k 1.3×	574 0.5×	139	10.4k
M. Daniele Fallin United States	54	3.8k 1.8×	2.8k 1.5×	1.3k 0.9×	571 0.5×	606 0.5×	199	10.0k
Gary E. Swan United States	63	3.7k 1.8×	1.3k 0.7×	666 0.5×	1.7k 1.4×	1.3k 1.2×	243	14.0k
Pierre Déchelotte France	60	3.5k 1.7×	1.2k 0.7×	478 0.4×	1.3k 1.0×	1.1k 1.0×	477	13.1k
Louise D. McCullough United States	79	5.6k 2.7×	1.1k 0.6×	1.0k 0.8×	1.1k 0.9×	3.7k 3.3×	378	20.6k
George Mastorakos Greece	55	1.3k 0.6×	616 0.3×	1.5k 1.1×	1.8k 1.5×	1.0k 0.9×	321	11.6k
Tom R. Gaunt United Kingdom	47	5.6k 2.7×	5.4k 2.9×	1.7k 1.2×	938 0.8×	1.5k 1.4×	200	13.8k
Louis J. Muglia United States	66	3.6k 1.8×	1.5k 0.8×	2.5k 1.8×	1.3k 1.1×	2.4k 2.2×	254	14.4k

Countries citing papers authored by David M. Hougaard

Since Specialization

Citations

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

Fields of papers citing papers by David M. Hougaard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David M. Hougaard. 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 David M. Hougaard. The network helps show where David M. Hougaard may publish in the future.

Co-authorship network of co-authors of David M. Hougaard

This figure shows the co-authorship network connecting the top 25 collaborators of David M. Hougaard. A scholar is included among the top collaborators of David M. Hougaard 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 David M. Hougaard. David M. Hougaard 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

Hagen, Christian M., Alfonso Buil, Emma Malchau Carlsen, et al.. (2024). Proteomic profiling of neonatal herpes simplex virus infection on dried blood spots. SHILAP Revista de lepidopterología. 4(1). 268–268.

Borbye‐Lorenzen, Nis, Filip Ottosson, Ron Nudel, et al.. (2024). High level of immunoglobulin G targeting mycoplasma or cytomegalovirus in the newborn increases risk of ADHD. Brain Behavior and Immunity. 123. 99–107. 2 indexed citations

Nielsen, Trine Tollerup, Jinjie Duan, Daniel F. Levey, et al.. (2024). Shared genetics of ADHD, cannabis use disorder and cannabis use and prediction of cannabis use disorder in ADHD. Nature Mental Health. 2(9). 1071–1083. 1 indexed citations

Ingason, Andrés, Christine Søholm Hansen, Marie Bækvad‐Hansen, et al.. (2023). T56. NEONATAL BLOOD TRANSCRIPTOMICS REVEAL EXPRESSION SIGNATURES OF ADHD RISK. European Neuropsychopharmacology. 75. S191–S192. 1 indexed citations

Hedley, Paula L., Gitte Hedermann, Marie Bækvad‐Hansen, et al.. (2023). The impact of the COVID-19 lockdown on birthweight among singleton term birth in Denmark. PLoS ONE. 18(4). e0283909–e0283909. 2 indexed citations

Li, Shaobo, Christian M. Hagen, Ulrik Kristoffer Stoltze, et al.. (2023). Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locus. Neuro-Oncology. 25(9). 1709–1720. 8 indexed citations

Nudel, Ron, David M. Hougaard, Thomas Werge, & Michael E. Benros. (2023). Genetic and epidemiological analyses of infection load and its relationship with psychiatric disorders. Epidemiology and Infection. 151. e93–e93. 2 indexed citations

Munch, Tina Nørgaard, Paula L. Hedley, Christian M. Hagen, et al.. (2022). The genetic background of hydrocephalus in a population-based cohort: implication of ciliary involvement. Brain Communications. 5(1). fcad004–fcad004. 3 indexed citations

Nudel, Ron, Wesley K. Thompson, Anders D. Børglum, et al.. (2022). Maternal pregnancy-related infections and autism spectrum disorder—the genetic perspective. Translational Psychiatry. 12(1). 334–334. 16 indexed citations

10.

Hedermann, Gitte, Paula L. Hedley, Marie Bækvad‐Hansen, et al.. (2020). Danish premature birth rates during the COVID-19 lockdown. Archives of Disease in Childhood Fetal & Neonatal. 106(1). 93–95. 187 indexed citations

11.

Rasmussen, Jon, Christian Selmer, Signe Frøssing, et al.. (2020). Endogenous Testosterone Levels Are Associated with Risk of Type 2 Diabetes in Women without Established Comorbidity. Journal of the Endocrine Society. 4(6). bvaa050–bvaa050. 18 indexed citations

12.

Aarøe, Lene, Vivek Appadurai, Kasper Møller Hansen, et al.. (2020). Genetic predictors of educational attainment and intelligence test performance predict voter turnout. Nature Human Behaviour. 5(2). 281–291. 21 indexed citations

13.

Østergaard, Søren Dinesen, Betina B. Trabjerg, Thomas D. Als, et al.. (2020). Polygenic risk score, psychosocial environment and the risk of attention-deficit/hyperactivity disorder. Translational Psychiatry. 10(1). 335–335. 23 indexed citations

14.

Nudel, Ron, Yunpeng Wang, Vivek Appadurai, et al.. (2019). A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population. Translational Psychiatry. 9(1). 283–283. 47 indexed citations

15.

Wimberley, Theresa, Esben Agerbo, Henriette Thisted Horsdal, et al.. (2019). Genetic liability to ADHD and substance use disorders in individuals with ADHD. Addiction. 115(7). 1368–1377. 43 indexed citations

16.

Hagen, Christian M., Vanessa F. Gonçalves, Paula L. Hedley, et al.. (2018). Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease. PLoS ONE. 13(12). e0208828–e0208828. 10 indexed citations

17.

Lundbo, Lene Fogt, Zitta Barrella Harboe, Louise Nygaard Clausen, et al.. (2015). Genetic Variation in NFKBIE Is Associated With Increased Risk of Pneumococcal Meningitis in Children. EBioMedicine. 3. 93–99. 16 indexed citations

18.

Eising, Stefanie, B Carstensen, Kristin Skogstrand, et al.. (2008). Perinatal factors and immunological markers at birth are associated to type 1 diabetes risk - a population-based study. Lund University Publications (Lund University). 3 indexed citations

19.

Sørensen, Karina Meden, Cathrine Jespersgaard, Jens Vuust, et al.. (2007). Whole Genome Amplification on DNA from Filter Paper Blood Spot Samples: An Evaluation of Selected Systems. Genetic Testing. 11(1). 65–71. 26 indexed citations

20.

Hougaard, David M.. (1992). Polyamine Cytochemistry: Localization and Possible Functions of Polyamines. International review of cytology. 138. 51–88. 37 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.

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