Guus Hamers

533 citations

19 papers · 393 indexed · h-index 12

Co-authors: J.J.M. Engelen Joep Geraedts C. T. R. M. Schrander‐Stumpel Patrick J. Willems H.-J. Lüdecke Bernhard Horsthemke M.J. Wagner Julia Parrish
Topics: Genomic variations and chromosomal abnormalities (12 papers)Prenatal Screening and Diagnostics (8 papers)Chromosomal and Genetic Variations (7 papers)
Cited by: Genetics Developmental Biology Pediatrics, Perinatology and Child Health
Journals: Human Molecular Genetics Human Reproduction Leukemia
Partner nations: Netherlands Belgium Germany

In The Last Decade

Guus Hamers

18 papers receiving 381 citations

Peers

Countries citing papers authored by Guus Hamers

Since Specialization

Citations

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

Fields of papers citing papers by Guus Hamers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guus Hamers

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis 2011 ·Molecular Cytogenetics ·Diane Van Opstal,Marjan Boter,(unknown),Malgorzata I. Srebniak,Guus Hamers,Robert‐Jan H. Galjaard	14
2	Sonographic genital ambiguity in a fetus due to a mosaic 45,X/46,X,idic(Y)(qter-p11.32::p11.32-qter) karyotype 2005 ·Prenatal Diagnosis ·(unknown),Guus Hamers,Antonius Mulder,(unknown),J. Offermans,J.J.M. Engelen,(unknown),Simon G. F. Robben,S de Muinck Keizer‐Schrama,Katja P. Wolffenbuttel,Leendert H. J. Looijenga,J. Wolter Oosterhuis,Connie Schrander‐Stumpel,J.G. Nijhuis	7
3	Translocation t(2;3)(p15–23;q26–27) in myeloid malignancies: report of 21 new cases, clinical, cytogenetic and molecular genetic features 2004 ·Leukemia ·Marian Stevens‐Kroef,Bruce Poppe,(unknown),Eva van den Berg,(unknown),Ad Geurts van Kessel,R Släter,Guus Hamers,Lucienne Michaux,Frank Speleman,A Hagemeijer	19
4	Mosaic trisomy 11p in monozygotic twins with discordant clinical phenotypes 2003 ·American Journal of Medical Genetics Part A ·(unknown),Guus Hamers,(unknown),J.G. Nijhuis,(unknown),J. Herbergs,Christine de Die‐Smulders,C. T. R. M. Schrander‐Stumpel,J.J.M. Engelen	11
5	Prenatal diagnosis of trisomy 12 mosaicism: normal development of a 3 years old female child. 2003 ·PubMed ·(unknown),(unknown),Guus Hamers,Jean‐Pierre Fryns	6
6	22q11 deletion: the Maastricht experience focussing on some unusual presentations 1999 ·C. T. R. M. Schrander‐Stumpel,Guus Hamers,J.J.M. Engelen,Suzanna G.M. Frints,J. Offermans,Jean‐Pierre Fryns	2
7	Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: Value of FISH over high resolution banding 1999 ·American Journal of Medical Genetics ·Christine de Die‐Smulders,J.J.M. Engelen,(unknown),Guus Hamers	2
8	Subfertile men with constitutive chromosome abnormalities do not necessarily refrain from intracytoplasmic sperm injection treatment: a follow-up study on 75 Dutch patients 1999 ·Human Reproduction ·Jacques C. Giltay,P.M.M. Kastrop,(unknown),Jan A.M. Kremer,(unknown),(unknown),(unknown),(unknown),Roel Hordijk,Guus Hamers,Kerstin Hansson,(unknown),L. Govaerts,M.H.E.C. Pieters,K. Madan,J. M. J. C. Scheres	21
9	A simple and efficient method for microdissection and microFISH. 1998 ·Journal of Medical Genetics ·J.J.M. Engelen,(unknown),Guus Hamers,Joep Geraedts	41
10	Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization 1998 ·American Journal of Medical Genetics ·J.J.M. Engelen,(unknown),(unknown),Astrid S. Plomp,S. B. van der Meer,J.S.H. Vles,Guus Hamers,Joep Geraedts	0
11	Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization 1998 ·American Journal of Medical Genetics ·J.J.M. Engelen,(unknown),(unknown),Astrid S. Plomp,S. B. van der Meer,J.S.H. Vles,Guus Hamers,Joep Geraedts	13
12	Marker chromosome identification by micro‐FISH 1996 ·Clinical Genetics ·J.J.M. Engelen,(unknown),(unknown),Ute Moog,Guus Hamers,Joep Geraedts	9
13	Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer--Giedion syndrome 1995 ·Human Molecular Genetics ·H.-J. Lüdecke,M.J. Wagner,(unknown),(unknown),Julia Parrish,Patrick J. Willems,E Haan,Moshe Frydman,Guus Hamers,(unknown),Bernhard Horsthemke	95
14	Human parvovirus B19 infection and unbalanced translocation in a case of hydrops fetalis 1994 ·Prenatal Diagnosis ·Christine Willekes,Frans J.M.E. Roumen,(unknown),H. T. Weiland,(unknown),J. Han van Krieken,Christine de Die‐Smulders,Guus Hamers,(unknown)	4
15	ICF syndrome: a new case and review of the literature 1994 ·Human Genetics ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Guus Hamers	79
16	The partial monosomy 10q syndrome: report on two patients and review of the developmental data 1991 ·Journal of Intellectual Disability Research ·Connie Schrander‐Stumpel,J P Fryns,Guus Hamers	19
17	Trisomy 17p due to a t(8; 17) (p23; p11.2)pat translocation. Case report and review of the literature 1990 ·Clinical Genetics ·C. T. R. M. Schrander‐Stumpel,J. J. P. Schrander,J. P. Fryns,Guus Hamers	20
18	Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping 1989 ·Human Genetics ·H. J. DE LIEFDE MEIJER,Guus Hamers,Roselie Jongbloed,(unknown),René R. W. J. van der Hulst,Joep Geraedts	12
19	Caudal deficiency sequence in 7q terminal deletion 1988 ·American Journal of Medical Genetics ·C. T. R. M. Schrander‐Stumpel,Jaap J.P. Schrander,Jean‐Pierre Fryns,Guus Hamers,John M. Opitz,James F. Reynolds	19

About Guus Hamers

Guus Hamers is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science, having authored 19 papers that have together received 393 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (8 papers) and Chromosomal and Genetic Variations (7 papers). The work is most often cited by research in Genetics (258 citations), Developmental Biology (11 citations) and Pediatrics, Perinatology and Child Health (89 citations). Guus Hamers has collaborated with scholars based in Netherlands, Belgium and Germany. Frequent co-authors include J.J.M. Engelen, Joep Geraedts, C. T. R. M. Schrander‐Stumpel, Patrick J. Willems, H.-J. Lüdecke, Bernhard Horsthemke, M.J. Wagner, Julia Parrish, E Haan and Moshe Frydman. Their work appears in journals such as Human Molecular Genetics, Human Reproduction and Leukemia.

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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