Bernard A. van Oost

8.6k total citations · 3 hit papers
134 papers, 6.4k citations indexed

About

Bernard A. van Oost is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Bernard A. van Oost has authored 134 papers receiving a total of 6.4k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 46 papers in Genetics and 15 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Bernard A. van Oost's work include Mitochondrial Function and Pathology (19 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Metabolism and Genetic Disorders (15 papers). Bernard A. van Oost is often cited by papers focused on Mitochondrial Function and Pathology (19 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Metabolism and Genetic Disorders (15 papers). Bernard A. van Oost collaborates with scholars based in Netherlands, United States and Germany. Bernard A. van Oost's co-authors include Hans‐Hilger Ropers, Marcel Nelen, Han G. Brunner, Xandra O. Breakefield, L.A.H. Monnens, Marian Verdijk, Bé Wieringa, Nine V.A.M. Knoers, C.H. van Os and Peter M.T. Deen and has published in prestigious journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Bernard A. van Oost

133 papers receiving 6.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A

1993 1.1k citations Han G. Brunner, Marcel Nelen et al. profile →
Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-dependent Concentration of Urine

1994 698 citations Marian Verdijk, L.A.H. Monnens et al. profile →
Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.

1996 542 citations Bernard A. van Oost et al. profile →

Peers

Countries citing papers authored by Bernard A. van Oost

Since Specialization

Citations

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

Fields of papers citing papers by Bernard A. van Oost

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bernard A. van Oost. 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 Bernard A. van Oost. The network helps show where Bernard A. van Oost may publish in the future.

Co-authorship network of co-authors of Bernard A. van Oost

This figure shows the co-authorship network connecting the top 25 collaborators of Bernard A. van Oost. A scholar is included among the top collaborators of Bernard A. van Oost 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 Bernard A. van Oost. Bernard A. van Oost 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

#	Work	Indexed citations
1	Evaluation of the Serotonergic Genes htr1A, htr1B, htr2A, and slc6A4 in Aggressive Behavior of Golden Retriever Dogs 2007 ·Behavior Genetics ·Linda van den Berg, (unknown), Matthijs B.H. Schilder, Bernard A. van Oost, H. A. W. Hazewinkel, Claire M. Wade, Elinor K. Karlsson, Kerstin Lindblad‐Toh, A.-E. Liinamo, Peter A. J. Leegwater	29
2	Localization of White Spotting Locus in Boxer Dogs on CFA20 by Genome-Wide Linkage Analysis with 1500 SNPs 2007 ·Journal of Heredity ·Peter A. J. Leegwater, (unknown), Bernard A. van Oost	14
3	19 Molecular Genetics of Dilated Cardiomyopathy 2006 ·Cold Spring Harbor Monograph Archive ·Polona Le Quesne Stabej, Kathryn M. Meurs, Bernard A. van Oost	0
4	Intestinal over-expression of iron transporters induces iron overload in birds in captivity 2005 ·Blood Cells Molecules and Diseases ·Aslı Mete, (unknown), Bernard A. van Oost, J. E. van Dijk, Joannes J.M. Marx	21
5	Chicken single nucleotide polymorphism identification and selection for genetic mapping 2004 ·Poultry Science ·(unknown), Ruben van’t Slot, Bernard A. van Oost	10
6	Typing Single-Nucleotide Polymorphisms Using a Gel-Based Sequencer: A New Data Analysis Tool and Suggestions for Improved Efficiency 2003 ·Molecular Biotechnology ·(unknown), A. Veenendaal, Bernard A. van Oost, M.F.W. te Pas, Martien A. M. Groenen	7
7	Mutation detection in the aspartoacylase gene in 17 patients with Canavan disease: four new mutations in the non-Jewish population 2000 ·European Journal of Human Genetics ·Erik A. Sistermans, I.F.M. de Coo, (unknown), Bwee Tien Poll‐The, Wim J. Kleijer, Bernard A. van Oost	33
8	A 4-base pair deletion in the mitochondrial cytochromeb gene associated with parkinsonism/MELAS overlap syndrome 1999 ·Annals of Neurology ·I.F.M. de Coo, W.O. Renier, W. Ruitenbeek, H. J. ter Laak, M. Bakker, (unknown), Bernard A. van Oost, H.J.M. Smeets	107
9	The Role of Molecular Genetics in the Diagnosis of Diseases in Companion Animals: An Introduction 1998 ·Veterinary Quarterly ·Bernard A. van Oost	2
10	Inheritance of mutations in the V2 receptor gene in thirteen families with nephrogenic diabetes insipidus 1994 ·Kidney International ·Nine Knoers, Ans M.W. van den Ouweland, Marian Verdijk, L.A.H. Monnens, Bernard A. van Oost	45
11	Identification of Four Novel Mutations in the COL4A5 Gene of Patients with Alport Syndrome 1993 ·Genomics ·Henny H. Lemmink, Cornelis H. Schröder, Han G. Brunner, Marcel Nelen, Jing Zhou, Karl Tryggvason, (unknown), (unknown), Wolfgang Rascher, Bernard A. van Oost, Hubert J.M. Smeets	20
12	X-linked myoclonus epilepsy explained as a maternally inherited mitochondrial disorder 1993 ·Human Genetics ·(unknown), Ilse J. de Wijs, (unknown), Uwe‐Peter Ketelsen, Hans‐Hilger Ropers, Bernard A. van Oost	4
13	A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome 1993 ·Annals of Neurology ·(unknown), Baziel G.M. van Engelen, F.J.M. Gabreëls, W. Ruitenbeek, Bernard A. van Oost	205
14	Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15 1992 ·New England Journal of Medicine ·Dominique Smeets, Ben C.J. Hamel, Marcel Nelen, H. Smeets, J. Bollen, Arie P.T. Smits, Hans‐Hilger Ropers, Bernard A. van Oost	105
15	Determination of sex ratio of spermatozoa with a deoxyribonucleic acid-probe and quinacrine staining: a comparison 1992 ·Fertility and Sterility ·R. J. van Kooij, Bernard A. van Oost	29
16	Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panel 1992 ·Genomics ·Heiko Traupe, (unknown), Bernard A. van Oost, (unknown), U. Vetter, Stephen T. Warren, Mariano Rocchi, Mark G. Darlison, Hans‐Hilger Ropers	38
17	Eye movement disorder: An early expression of the myotonic dystrophy gene? 1992 ·Muscle & Nerve ·J.P. ter Bruggen, Cees Tijssen, Han G. Brunner, Bernard A. van Oost, (unknown)	4
18	Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 region 1992 ·Genomics ·A.M.W. van den Ouweland, (unknown), V.V.A.M. Knoers, (unknown), Mariano Rocchi, Stephen T. Warren, Hans‐Hilger Ropers, Falk Fahrenholz, L.A.H. Monnens, Bernard A. van Oost	20
19	Validation of linkage‐based DNA‐diagnosis of fragile X gene carriers with the CGG repeat probe 1992 ·American Journal of Medical Genetics ·Bernard A. van Oost, Arie P.T. Smits, Jos Dreesen, Ans M.W. van den Ouweland, Ben A. Oostra	4
20	Linkage homogeneity near the fragile X locus in normal and fragile X families 1991 ·Genomics ·G K Suthers, John C. Mulley, Marie‐Antoinette Voelckel, Niklas Dahl, Marja‐Leena Väisänen, Peter Steinbach, Ian A. Glass, Charles E. Schwartz, Bernard A. van Oost, Stephen N. Thibodeau, N E Haites, B. A. Oostra, Albert Schinzel, Miguel Carballo, C. Phillip Morris, John J. Hopwood, G.R. Sutherland	11

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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