Jon Brynjolfsson

3.8k citations

33 papers · 1.1k indexed · h-index 13

Impact in

Genetics top 2%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Biological Psychiatry top 10%

Papers in

Genetics 20
- Genetic Associations and Epidemiology 12
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 6
- Genetic Syndromes and Imprinting 2
Psychiatry and Mental health 9
- Bipolar Disorder and Treatment 7

Co-authors: Hannes Pétursson Robin Sherrington David Curtis Hugh Gurling Mark D. Potter H. Gurling John J. Wasmuth Keith E. Dudleston
Journals: Psychiatric Genetics (8 papers)American Journal of Psychiatry (3 papers)The British Journal of Psychiatry (3 papers)Annals of Human Genetics (2 papers)Biological Psychiatry (2 papers)
Partner nations: United Kingdom Iceland United States

In The Last Decade

Jon Brynjolfsson

33 papers receiving 1.0k citations

Peers

Countries citing papers authored by Jon Brynjolfsson

Since Specialization

Citations

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

Fields of papers citing papers by Jon Brynjolfsson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jon Brynjolfsson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jon Brynjolfsson Line = papers co-authored together Jon Brynjolfsson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23-q24, and suggests the presence of additional loci on 1p and 1q Psychiatric Genetics ·David Curtis, Gursharan Kalsi, Jon Brynjolfsson, Melvin G. McInnis, Jane O’Neill, Leonor Avila Brizuela, A. Giacalone, Patrice Murphy, Andrew McQuillin, Hannes Pétursson, Hugh Gurling	2003	125
2	Genome wide linkage anlaysis supports the presence of two separate susceptibility loci on chromosome 1q32 for biopolar disorder and 1q21-22.3 for schizophrenia American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Hugh Gurling, David Curtis, G. Kalsi, Andrew McQuillin, Jacob Lawrence, P. Murphy, Jon Brynjolfsson, M. G. McInnis, 赵栓柱, Hannes Pétursson	2000	1
3	No evidence for linkage of schizophrenia to DXS7 at chromosome Xp11 Psychiatric Genetics ·G. Kalsi, Guy Pantel, David Curtis, Jon Brynjolfsson, 赵栓柱, Robert J. Butler, Timothy Read, P. Murphy, Hannes Pétursson, Hmd Gurling	1999	2
4	New DNA markers with increased informativeness show diminished support for a chromosome 5q11–13 schizophrenia susceptibility locus and exclude linkage in two new cohorts of British and Icelandic families Annals of Human Genetics ·Gursharan Kalsi, Baljinder S. Mankoo, David Curtis, Robin Sherrington, Georg Melmer, Jon Brynjolfsson, 赵栓柱, Timothy D. Read, P. Murphy, Hannes Pétursson, H. Gurling	1999	11
5	No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins Human Genetics ·Patricia Fernández Cuadrado, Gursharan Kalsi, Timothy A. Klempan, Michał Hess, E. Ewe, T. Breschel, M. G. McInnis, Jon Brynjolfsson, Hannes Pétursson, Hmd Gurling, Irving I. Gottesman, Ε. Fuller Torrey, Artūras Petronis, James L. Kennedy	1998	26
6	Tests of linkage, allelic and genotypic association between schizophrenia and the gene for the D3 dopamine receptor, DRD3 Psychiatric Genetics ·Gursharan Kalsi, David Curtis, Jon Brynjolfsson, 赵栓柱, Hannes Pétursson, Robert J. Butler, Timothy D. Read, P. Murphy, Hmd Gurling	1998	3
7	Test of Xq26.3–28 linkage in bipolar and unipolar affective disorder in families selected for absence of male to male transmission The British Journal of Psychiatry ·Leonor Avila Brizuela, Gursharan Kalsi, Jon Brynjolfsson, Jane O’Neill, David Curtis, Larry Rifkin, Sudharsana Sundarrajan, Patrice Murphy, Hannes Pétursson, Hugh Gurling	1997	10
8	Two-Locus Admixture Linkage Analysis of Bipolar and Unipolar Affective Disorder Supports the Presence of Susceptibility Loci on Chromosomes 11p15 and 21q22 Genomics ·Leonor Avila Brizuela, Katri Nelo, David Curtis, Jon Brynjolfsson, Jane O’Neill, Larry Rifkin, Sudharsana Sundarrajan, P. L. Murphy, Hannes Pétursson, Hugh Gurling	1997	70
9	Exclusion of linkage between schizophrenia and the gene encoding a neutral amino acid glutamate/aspartate transporter, SLC1A5 American Journal of Medical Genetics ·Basel Saleh, Gursharan Kalsi, Jon Brynjolfsson, Thordur Sigmundsson, David Curtis, Robert J. Butler, Tim Read, Patrice Murphy, Eric A. Barnard, Hannes Pétursson, Hugh Gurling	1997	1
10	Linkage Analysis of Manic Depression (Bipolar Affective Disorder) in Icelandic and British Kindreds using Markers on the Short Arm of Chromosome 18 Human Heredity ·Gursharan Kalsi, Leonor Avila Brizuela, Jon Brynjolfsson, Luis León-Trejo, Massimo Sanna, David Curtis, Larry Rifkin, P. Murphy, Hannes Pétursson, Hyun-Dong Pai	1997	14
11	Linkage analysis of chromosome 22q12–13 in a United Kingdom/Icelandic sample of 23 multiplex schizophrenia families American Journal of Medical Genetics ·Gursharan Kalsi, Jon Brynjolfsson, Robert J. Butler, Robin Sherrington, David Curtis, Thordur Sigmundsson, Timothy Read, P. Murphy, T. Sharma, Hannes Pétursson, Hmd Gurling	1995	32
12	Exclusion of linkage of schizophrenia to the gene for the dopamine D2 receptor (DRD2) and chromosome 11q translocation sites Psychological Medicine ·Gursharan Kalsi, Wolde-Senbet Abinet, David Curtis, Jon Brynjolfsson, Timothy Read, Lúcia Maria Soares de Azevedo, P. Murphy, Hannes Pétursson, Hmd Gurling	1995	12
13	Investigation by Linkage Analysis of the XY Pseudoautosomal Region in the Genetic Susceptibility to Schizophrenia The British Journal of Psychiatry ·Gursharan Kalsi, David Curtis, Jon Brynjolfsson, Robert J. Butler, Tonmoy Sharma, Sven Zehnder, Tim Read, Hannes Pétursson, Hugh Gurling	1995	10
14	The Marfan syndrome gene locus as a favoured locus for susceptibility to schizophrenia Psychiatric Genetics ·Gursharan Kalsi, Baljinder S. Mankoo, Jon Brynjolfsson, David Curtis, Timothy Read, P. L. Murphy, Lúcia Maria Soares de Azevedo, Hannes Pétursson, Hugh Gurling	1994	12
15	A linkage study of affective disorder with DNA markers for the ABO-AK1-ORM linkage group near the dopamine beta hydroxylase gene Biological Psychiatry ·Robin Sherrington, David Curtis, Jon Brynjolfsson, Felipe Ramos Caldeira, Larry Rifkin, Hannes Pétursson, H. Gurling	1994	3
16	Linkage between tyrosine hydroxylase gene and affective disorder cannot be excluded in two of six pedigrees American Journal of Medical Genetics ·Lionel Lim, Hugh Gurling, David Curtis, Jon Brynjolfsson, Hannes Pétursson, Michael Gill	1993	39
17	Segregation and linkage analysis in five manic depression pedigrees excludes the 5HT1a receptor gene (HTR1A) Annals of Human Genetics ·David Curtis, Jon Brynjolfsson, Hannes Pétursson, Susan Holmes, Robin Sherrington, Peter Brett, Larry Rifkin, P. Murphy, Felipe Ramos Caldeira, Georg Melmer, Hugh Gurling	1993	15
18	Recent and Future Molecular Genetic Research Into Schizophrenia Schizophrenia Bulletin ·Hugh Gurling, Robin Sherrington, Jon Brynjolfsson, Timothy Read, David Curtis, L. Acosta Gorrin, Mark D. Potter, Hannes Pétursson	1989	6
19	Molecular genetics and heterogeneity in manic depression Molecular Neurobiology ·Hugh Gurling, Robin Sherrington, Jon Brynjolfsson, Mark D. Potter, Melvin G. McInnis, Hannes Pétursson, S. Hodgkinson	1988	5
20	Localization of a susceptibility locus for schizophrenia on chromosome 5 Nature ·Robin Sherrington, Jon Brynjolfsson, Hannes Pétursson, Mark D. Potter, Keith E. Dudleston, B. M. Barraclough, John J. Wasmuth, Roberta A. Wright, H. Gurling	1988	402

About Jon Brynjolfsson

Jon Brynjolfsson is a scholar working on Genetics, Psychiatry and Mental health, Biochemistry, Biological Psychiatry and Cellular and Molecular Neuroscience, having authored 33 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (12 papers), Bipolar Disorder and Treatment (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Neuroscience and Neuropharmacology Research (4 papers), Autism Spectrum Disorder Research (4 papers), Amino Acid Enzymes and Metabolism (3 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Genetics (727 citations), Biological Psychiatry (54 citations), Psychiatry and Mental health (302 citations), Cellular and Molecular Neuroscience (181 citations) and Cognitive Neuroscience (109 citations). Jon Brynjolfsson has collaborated with scholars based in United Kingdom, Iceland and United States. Frequent co-authors include Hannes Pétursson, Robin Sherrington, David Curtis, Hugh Gurling, Mark D. Potter, H. Gurling, John J. Wasmuth, Keith E. Dudleston, B. M. Barraclough and Gursharan Kalsi. Their work appears in journals such as Psychiatric Genetics, American Journal of Psychiatry, The British Journal of Psychiatry, Annals of Human Genetics and Biological Psychiatry.

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