A.J.H. Hamers

816 total citations
33 papers, 560 citations indexed

About

A.J.H. Hamers is a scholar working on Genetics, Plant Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, A.J.H. Hamers has authored 33 papers receiving a total of 560 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 16 papers in Plant Science and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in A.J.H. Hamers's work include Genomic variations and chromosomal abnormalities (26 papers), Chromosomal and Genetic Variations (16 papers) and Prenatal Screening and Diagnostics (15 papers). A.J.H. Hamers is often cited by papers focused on Genomic variations and chromosomal abnormalities (26 papers), Chromosomal and Genetic Variations (16 papers) and Prenatal Screening and Diagnostics (15 papers). A.J.H. Hamers collaborates with scholars based in Netherlands, Belgium and Germany. A.J.H. Hamers's co-authors include J.J.M. Engelen, P.H. Jongbloet, Rune R. Frants, Ute Moog, Christine de Die‐Smulders, Aldur W. Eriksson, J.L.H. Evers, Yvonne Arens, K. Madan and D F Smeets and has published in prestigious journals such as The Lancet, Developmental Medicine & Child Neurology and Journal of Medical Genetics.

In The Last Decade

A.J.H. Hamers

33 papers receiving 515 citations

Peers

A.J.H. Hamers

GENET

PPCH

GENET

Sophie Brisset France

M. G. Daker United Kingdom

Simona Cavani Italy

Carrie Hanscom United States

Renata Gaillyová Czechia

Jürgen Kunze Germany

Mauro Pierluigi Italy

Roberto Quadrelli United States

J. M. Cant� Mexico

Mónica Rosello Spain

Sophie Brisset France

A.J.H. Hamers

378 ×0.9

GENET

194 ×0.9

183 ×0.9

PPCH

133 ×0.7

52 ×0.9

GENET

Citations per year, relative to A.J.H. Hamers A.J.H. Hamers (= 1×) peers Sophie Brisset

Countries citing papers authored by A.J.H. Hamers

Since Specialization

Citations

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

Fields of papers citing papers by A.J.H. Hamers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A.J.H. Hamers. 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 A.J.H. Hamers. The network helps show where A.J.H. Hamers may publish in the future.

Co-authorship network of co-authors of A.J.H. Hamers

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Arens, Yvonne, et al.. (2004). Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1‐5q31.3 in ten unbalanced carriers. American Journal of Medical Genetics Part A. 130A(2). 128–133. 28 indexed citations

Engelen, J.J.M., et al.. (2003). Characterization of a chromosome 8‐derived minute marker chromosome using microdissection and FISH in a boy with growth retardation. American Journal of Medical Genetics Part A. 118A(3). 274–278. 4 indexed citations

Engelen, J.J.M., et al.. (2003). Intrachromosomal insertion translocation resulting in duplication of chromosome band Yq11.2 in two fertile brothers. American Journal of Medical Genetics Part A. 118A(3). 287–289. 21 indexed citations

Engelen, J.J.M., Christine de Die‐Smulders, W.M.A. Verhoeven, et al.. (2002). Duplication of chromosome region (16)(p11.2 → p12.1) in a mother and daughter with mild mental retardation. American Journal of Medical Genetics. 109(2). 149–153. 17 indexed citations

Engelen, J.J.M., et al.. (2001). De novo ?pure? partial trisomy (6)(p22.1?pter) in a chromosome 15 with an enlarged satellite, identified by microdissection. American Journal of Medical Genetics. 99(1). 48–53. 20 indexed citations

Sánchez-García, Jorge F., et al.. (2001). De novo duplication (5)(q31.3q33.3): report of a patient and characterization of the duplicated region using microdissection and FISH. American Journal of Medical Genetics. 100(1). 56–61. 10 indexed citations

Stevens‐Kroef, Marian, et al.. (2000). Complex Chromosome 9, 20, and 22 Rearrangements in Acute Lymphoblastic Leukemia with Duplication of BCR and ABL Sequences. Cancer Genetics and Cytogenetics. 116(2). 119–123. 4 indexed citations

Hamers, A.J.H., Roel Hordijk, Kerstin Hansson, et al.. (1998). Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience. European Journal of Human Genetics. 6(3). 194–200. 82 indexed citations

Engelen, J.J.M., et al.. (1996). Application of micro-FISH to delineate deletions. Cytogenetic and Genome Research. 75(2-3). 167–171. 12 indexed citations

10.

Engelen, J.J.M., et al.. (1995). Familial partial trisomy 8p without dysmorphic features and only mild mental retardation. Journal of Medical Genetics. 32(10). 792–795. 28 indexed citations

11.

Engelen, J.J.M., et al.. (1994). Partial trisomy and monosomy 8p due to inversion duplication. Clinical Genetics. 45(4). 203–207. 16 indexed citations

12.

Moog, Ute, et al.. (1994). Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication. Clinical Genetics. 46(6). 423–429. 38 indexed citations

13.

Engelen, J.J.M., A.J.H. Hamers, C. T. R. M. Schrander‐Stumpel, H.A. Mulder, & Ben J. H. M. Poorthuis. (1992). Assignment of the aspartylglucosaminidase gene (AGA) to 4q33→q35 based on decreased activity in a girl with a 46, XX, del(4)(q33) karyotype. Cytogenetic and Genome Research. 60(3-4). 208–209. 5 indexed citations

14.

Hamers, A.J.H., Bauke M. de Jong, R.F. Suijkerbuijk, et al.. (1991). A 46,XY female with mixed gonadal dysgenesis and a 48,XY,+7,+i(12p) chromosome pattern in a primary gonadal tumor. Cancer Genetics and Cytogenetics. 57(2). 219–224. 15 indexed citations

15.

Andel, J.F. de Rijk-van, Coriene E. Catsman‐Berrevoets, J. O. Van Hemel, & A.J.H. Hamers. (1991). Clinical and Chromosome Studies of Three Patients with Smith‐Magenis Syndrome. Developmental Medicine & Child Neurology. 33(4). 343–347. 25 indexed citations

16.

Madan, K., M.H.E.C. Pieters, L. P. Kuyt, et al.. (1990). Paracentric inversion inv(11) (q21q23) in the Netherlands. Human Genetics. 85(1). 15–20. 11 indexed citations

17.

Hamers, A.J.H., et al.. (1990). Severe mental retardation in a patient with tricho-rhino-phalangeal syndrome type I and 8q deletion. European Journal of Pediatrics. 149(9). 618–620. 17 indexed citations

18.

Hamers, A.J.H., Hans‐Peter Meyer, R. J. E. Jongbloed, René R. W. J. van der Hulst, & Joep Geraedts. (1990). Rate of recombination of chromosomes 21 in parents of children with Down syndrome. Clinical Genetics. 37(6). 463–469. 3 indexed citations

19.

Hamers, A.J.H., et al.. (1987). On the origin of recurrent trisomy 21: determination using chromosomal and DNA polymorphisms. Clinical Genetics. 32(6). 409–413. 10 indexed citations

20.

Jongbloet, P.H., et al.. (1982). Seasonality of pre-ovulatory non-disjunction and the aetiology of Down syndrome. A European collaborative study. Human Genetics. 62(2). 134–8. 20 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.

Explore authors with similar magnitude of impact