Harm Boer

2.5k total citations
35 papers, 1.6k citations indexed

About

Harm Boer is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Clinical Psychology. According to data from OpenAlex, Harm Boer has authored 35 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 9 papers in Pediatrics, Perinatology and Child Health and 6 papers in Clinical Psychology. Recurrent topics in Harm Boer's work include Genetic Syndromes and Imprinting (23 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Prenatal Screening and Diagnostics (9 papers). Harm Boer is often cited by papers focused on Genetic Syndromes and Imprinting (23 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Prenatal Screening and Diagnostics (9 papers). Harm Boer collaborates with scholars based in United Kingdom, Netherlands and Australia. Harm Boer's co-authors include David Clarke, Anthony Holland, J. Whittington, T. Webb, Jill Butler, T. Webb, Sarita Soni, Esther N. Maina, Leopold Curfs and Man Cheung Chung and has published in prestigious journals such as The British Journal of Psychiatry, Psychological Medicine and Clinical Neurophysiology.

In The Last Decade

Harm Boer

33 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Harm Boer United Kingdom 19 1.4k 420 416 309 159 35 1.6k
Elizabeth Roof United States 16 889 0.6× 293 0.7× 277 0.7× 201 0.7× 93 0.6× 29 1.0k
Eric Smeets Netherlands 22 902 0.6× 517 1.2× 411 1.0× 89 0.3× 66 0.4× 62 1.2k
Louise R. Greenswag United States 6 1.2k 0.8× 119 0.3× 473 1.1× 382 1.2× 150 0.9× 9 1.3k
Silvana Beri Italy 19 473 0.3× 130 0.3× 397 1.0× 232 0.8× 54 0.3× 34 1.0k
Jeanne M. Hanchett United States 6 947 0.7× 98 0.2× 392 0.9× 301 1.0× 124 0.8× 7 1.1k
John T. Martsolf United States 23 411 0.3× 144 0.3× 193 0.5× 689 2.2× 54 0.3× 38 1.2k
Alison D. Archibald Australia 21 545 0.4× 317 0.8× 194 0.5× 245 0.8× 62 0.4× 55 978
Ave M. Lachiewicz United States 23 1.6k 1.1× 1.2k 2.9× 784 1.9× 127 0.4× 47 0.3× 38 1.9k
Urs Eiholzer Switzerland 26 1.2k 0.8× 60 0.1× 591 1.4× 492 1.6× 234 1.5× 57 1.7k
Gwénaëlle Diene France 23 1.1k 0.8× 88 0.2× 483 1.2× 292 0.9× 307 1.9× 55 1.5k

Countries citing papers authored by Harm Boer

Since Specialization
Citations

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

Fields of papers citing papers by Harm Boer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Harm Boer

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

All Works

20 of 20 papers shown
1.
2.
Boer, Harm, Regi Alexander, John Devapriam, et al.. (2016). Prisoner mental health care for people with intellectual disability. International Journal of Culture and Mental Health. 9(4). 442–446. 5 indexed citations
3.
Sinnema, Margje, Marian A. Maaskant, H. M. J. van Schrojenstein Lantman‐de Valk, et al.. (2013). The use of medical care and the prevalence of serious illness in an adult Prader–Willi syndrome cohort. European Journal of Medical Genetics. 56(8). 397–403. 12 indexed citations
4.
Sinnema, Margje, et al.. (2012). Aging in Prader–Willi syndrome: Twelve persons over the age of 50 years. American Journal of Medical Genetics Part A. 158A(6). 1326–1336. 22 indexed citations
5.
Sinnema, Margje, Stewart Einfeld, C. T. R. M. Schrander‐Stumpel, et al.. (2011). Behavioral phenotype in adults with Prader–Willi syndrome. Research in Developmental Disabilities. 32(2). 604–612. 63 indexed citations
6.
Khan, Faheem Ahmed, et al.. (2011). What's in a name? - The Psychiatric Identity Conundrum.. PubMed. 23 Suppl 1. S178–81. 3 indexed citations
7.
Soni, Sarita, J. Whittington, Anthony Holland, et al.. (2008). The phenomenology and diagnosis of psychiatric illness in people with Prader–Willi syndrome. Psychological Medicine. 38(10). 1505–1514. 115 indexed citations
8.
Webb, Tessa, Esther N. Maina, Sarita Soni, et al.. (2008). In search of the psychosis gene in people with Prader‐Willi syndrome. American Journal of Medical Genetics Part A. 146A(7). 843–853. 24 indexed citations
9.
Maina, Esther N., Tessa Webb, Sarita Soni, et al.. (2007). Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter. Journal of Human Genetics. 52(4). 297–307. 15 indexed citations
10.
Collin, Philippe, Harm Boer, Annick Vogels, & L.M.G. Curfs. (2005). Psychosis in children with the Prader-Willi syndrome. Journal of Applied Research in Intellectual Disabilities. 19(3). 254–254. 1 indexed citations
11.
Webb, T., J. Whittington, A J Holland, et al.. (2005). CD36 expression and its relationship with obesity in blood cells from people with and without Prader–Willi syndrome. Clinical Genetics. 69(1). 26–32. 5 indexed citations
12.
Whittington, J., Anthony Holland, T. Webb, et al.. (2004). Cognitive abilities and genotype in a population‐based sample of people with Prader–Willi syndrome. Journal of Intellectual Disability Research. 48(2). 172–187. 121 indexed citations
13.
Holland, Anthony, J. Whittington, Jill Butler, et al.. (2002). Behavioural phenotypes associated with specific genetic disorders: evidence from a population-based study of people with Prader-Willi syndrome. Psychological Medicine. 33(1). 141–153. 139 indexed citations
14.
Holland, A J, et al.. (2002). Prevalence of, and risk factors for, physical ill-health in people with Prader-Willi syndrome: a population-based study. Developmental Medicine & Child Neurology. 44(4). 248–248. 165 indexed citations
15.
Webb, T., J. Whittington, David Clarke, et al.. (2002). A study of the influence of different genotypes on the physical and behavioral phenotypes of children and adults ascertained clinically as having PWS. Clinical Genetics. 62(4). 273–281. 38 indexed citations
16.
Boer, Harm, et al.. (2002). Prader–Willi syndrome, compulsive and ritualistic behaviours: the first population-based survey. The British Journal of Psychiatry. 180(4). 358–362. 111 indexed citations
17.
Butler, Jill, J. Whittington, Anthony Holland, et al.. (2002). Prevalence of, and risk factors for, physical ill‐health in people with Prader‐Willi syndrome: a population‐based study. Developmental Medicine & Child Neurology. 44(4). 248–255. 209 indexed citations
18.
Bouras, Nick, David Clarke, Harm Boer, et al.. (1998). Prader–Willi syndrome and psychotic symptoms: I. Case descriptions and genetic studies*. Journal of Intellectual Disability Research. 42(6). 440–450. 31 indexed citations
19.
Clarke, David & Harm Boer. (1998). Problem Behaviors Associated With Deletion Prader-Willi, Smith-Magenis, and Cri Du Chat Syndromes. American Journal on Mental Retardation. 103(3). 264–264. 40 indexed citations
20.
Clarke, David, Harm Boer, Man Cheung Chung, Peter Sturmey, & T. Webb. (1996). Maladaptive behaviour in Prader‐Willi syndrome in adult life. Journal of Intellectual Disability Research. 40(2). 159–165. 80 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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