Merryn Macville

3.1k total citations
49 papers, 1.7k citations indexed

About

Merryn Macville is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Merryn Macville has authored 49 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 19 papers in Molecular Biology and 19 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Merryn Macville's work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (18 papers) and Fetal and Pediatric Neurological Disorders (11 papers). Merryn Macville is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (18 papers) and Fetal and Pediatric Neurological Disorders (11 papers). Merryn Macville collaborates with scholars based in Netherlands, United States and Sweden. Merryn Macville's co-authors include Evelin Schröck, Thomas Ried, Hesed Padilla‐Nash, Gert Auer, Kerstin Heselmeyer, Β. Michael Ghadimi, Catherine L. Keck, D.B. Zimonjic, N.C. Popescu and Harald Blegen and has published in prestigious journals such as The American Journal of Human Genetics, American Journal of Obstetrics and Gynecology and Journal of neurosurgery.

In The Last Decade

Merryn Macville

47 papers receiving 1.6k citations

Peers

Countries citing papers authored by Merryn Macville

Since Specialization

Citations

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

Fields of papers citing papers by Merryn Macville

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Merryn Macville

This figure shows the co-authorship network connecting the top 25 collaborators of Merryn Macville. A scholar is included among the top collaborators of Merryn Macville 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 Merryn Macville. Merryn Macville 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

#	Work	Indexed citations
1	Performance of non‐invasive prenatal testing in vanishing‐twin and multiple pregnancies: results of TRIDENT ‐2 study 2025 ·Ultrasound in Obstetrics and Gynecology ·(unknown), Caroline J. Bax, (unknown), (unknown), (unknown), Diane Van Opstal, Elles M. J. Boon, Merryn Macville, Mireille N. Bekker, Robert‐Jan H. Galjaard	0
2	Clinically Irrelevant Terminal 16q21 Deletion Detected by NIPT Is Attributable to Inherited Fragility at FRA16B 2025 ·American Journal of Medical Genetics Part A ·Servi J.C. Stevens, (unknown), Nicole Y. Souren, Merryn Macville, (unknown), Brigitte H. W. Faas, Bart de Koning, Arthur van den Wijngaard, Sonja de Munnik, Masoud Zamani Esteki	0
3	Fetal fraction of cell-free DNA in noninvasive prenatal testing and adverse pregnancy outcomes: a nationwide retrospective cohort study of 56,110 pregnant women 2023 ·American Journal of Obstetrics and Gynecology ·(unknown), P Scheffer, Jens Henrichs, Caroline J. Bax, Neeltje Crombag, Marjan M. Weiss, Merryn Macville, Diane Van Opstal, Elles M. J. Boon, Erik A. Sistermans, Lidewij Henneman, Ewoud Schuit, Mireille N. Bekker	10
4	Trial by Dutch laboratories for evaluation of non‐invasive prenatal testing. Part I—clinical impact 2016 ·Prenatal Diagnosis ·Dick Oepkes, Godelieve C.M.L. Page‐Christiaens, Caroline J. Bax, Mireille N. Bekker, Catia M. Bilardo, Elles M. J. Boon, G. Heleen Schuring‐Blom, A. Coumans, Brigitte H. W. Faas, Robert‐Jan H. Galjaard, Attie T. J. I. Go, Lidewij Henneman, Merryn Macville, Eva Pajkrt, Ron F. Suijkerbuijk, Karin Huijsdens–van Amsterdam, Diane Van Opstal, E. J. T. Verweij, Marjan M. Weiss, Erik A. Sistermans	110
5	Trial by Dutch laboratories for evaluation of non‐invasive prenatal testing. Part II—women's perspectives 2016 ·Prenatal Diagnosis ·Rachèl V. van Schendel, Godelieve C.M.L. Page‐Christiaens, Lean Beulen, Catia M. Bilardo, Marjon A. de Boer, A. Coumans, Brigitte H. W. Faas, Irene M. van Langen, Klaske D. Lichtenbelt, Merel C. van Maarle, Merryn Macville, Dick Oepkes, Eva Pajkrt, Lidewij Henneman	55
6	Absence of Heterozygosity Due to Template Switching during Replicative Rearrangements 2015 ·The American Journal of Human Genetics ·Claudia M.B. Carvalho, Rolph Pfundt, Daniel A. King, Sarah Lindsay, Luciana W. Zuccherato, Merryn Macville, Pengfei Liu, Diana Johnson, Paweł Stankiewicz, Chester Brown, Chad A. Shaw, Matthew E. Hurles, Grzegorz Ira, P. J. Hastings, Han G. Brunner, James R. Lupski	42
7	Intrachromosomal homologous recombination between inverted amplicons on opposing Y-chromosome arms 2013 ·Genomics ·Julian Lange, Michiel J. Noordam, Saskia K.M. van Daalen, Helen Skaletsky, Brian A. Clark, Merryn Macville, David C. Page, Sjoerd Repping	18
8	Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012 2013 ·Human Reproduction Update ·(unknown), Luc Smits, (unknown), Christine de Die‐Smulders, Aimée Paulussen, Merryn Macville, A. Coumans, Suzanna G.M. Frints	56
9	Economic evaluation of multiplex ligation-dependent probe amplification and karyotyping in prenatal diagnosis: a cost-minimization analysis 2011 ·Archives of Gynecology and Obstetrics ·(unknown), Erwin Birnie, Mariëtte J.V. Hoffer, Merryn Macville, Robert‐Jan Galjaard, G. Heleen Schuring‐Blom, (unknown), (unknown), Arie P.T. Smits, J. M. M. van Lith	4
10	Paternal origin of the de novo constitutional t(11;22)(q23;q11) 2010 ·European Journal of Human Genetics ·Tamae Ohye, Hidehito Inagaki, Hiroshi Kogo, Makiko Tsutsumi, Takema Kato, Maoqing Tong, Merryn Macville, Līvija Medne, Elaine H. Zackai, Beverly S. Emanuel, Hiroki Kurahashi	38
11	Spectral Karyotypic and Comparative Genomic Analysis of the Endocrine Pancreatic Tumor Cell Line BON-1 2009 ·Neuroendocrinology ·(unknown), Sandra M.H. Claessen, Merryn Macville, (unknown), Britt Skogseid, Ernst‐Jan M. Speel	14
12	XX male with sex reversal and a de novo 11;22 translocation 2006 ·American Journal of Medical Genetics Part A ·Merryn Macville, (unknown), (unknown), Erik Huys, Eric Schoenmakers, (unknown), Beverly S. Emanuel, J.J.M. Engelen	3
13	Novel murine B‐cell lymphoma/leukemia model to study BCL2‐driven oncogenesis 2005 ·International Journal of Cancer ·Jules P.P. Meijerink, Esther M.M. Van Lieshout, H. Berna Beverloo, Ellen van Drunen, E. J. B. M. Mensink, Merryn Macville, Rob Pieters	14
14	Numerical aberrations of chromosome 1 in cervical intraepithelial neoplasia are strongly associated with infection with high‐risk human papillomavirus types 2002 ·The Journal of Pathology ·Johan Bulten, Willem J. G. Melchers, (unknown), (unknown), Pino J. Poddighe, (unknown), Merryn Macville, Leon F.A.G. Massuger, Judith M. J. E. Bakkers, Antonius G.J.M. Hanselaar	12
15	Identification of Subgroups of High-grade Oligodendroglial Tumors by Comparative Genomic Hybridization 1999 ·Journal of Neuropathology & Experimental Neurology ·Judith W. M. Jeuken, Sandra H. E. Sprenger, Pieter Wesseling, Merryn Macville, Andreas von Deimling, Hans L. J. M. Teepen, Jacobus J. van Overbeeke, Rudolf H. Boerman	85
16	Molecular cytogenetic analysis of the bladder carcinoma cell line BK-10 by spectral karyotyping 1999 ·Genes Chromosomes and Cancer ·Hesed Padilla‐Nash, William G. Nash, George M. Padilla, (unknown), Cary N. Robertson, Merryn Macville, (unknown), Thomas Ried	36
17	Cytogenetic and molecular characterization of random chromosomal rearrangements activating the drug resistance gene,MDR1/P-glycoprotein, in drug-selected cell lines and patients with drug refractory ALL 1998 ·Genes Chromosomes and Cancer ·Turid Knutsen, Lyn A. Mickley, Thomas Ried, Eric D. Green, Stanislas du Manoir, Evelin Schröck, Merryn Macville, Yi Ning, Robert W. Robey, Mihael H. Polymeropoulos, Rosarelis Torres, Tito Fojo	62
18	Spectral karyotyping, a 24-colour FISH technique for the identification of chromosomal rearrangements 1997 ·Histochemistry and Cell Biology ·Merryn Macville, Timothy Veldman, Hesed Padilla‐Nash, Danny Wangsa, Patricia C. O’Brien, Evelin Schröck, Thomas Ried	65
19	Localization by fluorescence in situ hybridization (FISH) of human mitochondrial polymerase γ (POLG) to human chromosome band 15q24→q26, and of mouse mitochondrial polymerase γ (<i>Pol</i><i>g</i>) to mouse chromosome band 7E, with confirmation by direct sequence analysis of bacterial artificial chromosomes (BACs) 1997 ·Cytogenetic and Genome Research ·Steven J. Zullo, L. O. Butler, Robert J. Zahorchak, Merryn Macville, Cyril Denby Wilkes, Carl R. Merril	16
20	Evaluation of pepsin treatment for electron microscopic RNA in situ hybridization on ultra-thin cryosections of cultured cells 1996 ·Histochemistry and Cell Biology ·Merryn Macville, (unknown), Roeland W. Dirks, Jack Fransen, Anton K. Raap	5

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