Philippe Moerman

4.1k total citations
106 papers, 2.6k citations indexed

About

Philippe Moerman is a scholar working on Surgery, Genetics and Molecular Biology. According to data from OpenAlex, Philippe Moerman has authored 106 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Surgery, 30 papers in Genetics and 25 papers in Molecular Biology. Recurrent topics in Philippe Moerman's work include Prenatal Screening and Diagnostics (13 papers), Urological Disorders and Treatments (13 papers) and Congenital Diaphragmatic Hernia Studies (12 papers). Philippe Moerman is often cited by papers focused on Prenatal Screening and Diagnostics (13 papers), Urological Disorders and Treatments (13 papers) and Congenital Diaphragmatic Hernia Studies (12 papers). Philippe Moerman collaborates with scholars based in Belgium, United States and Netherlands. Philippe Moerman's co-authors include Joseph M. Lauweryns, Jean‐Pierre Fryns, Frédéric Amant, Ignace Vergote, Kamiel Vandenberghe, M Renaer, André Van Assche, L Carreras, Jos Vermylen and Frank de Wolf and has published in prestigious journals such as SHILAP Revista de lepidopterología, The EMBO Journal and American Journal of Obstetrics and Gynecology.

In The Last Decade

Philippe Moerman

105 papers receiving 2.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Philippe Moerman Belgium	25	819	508	495	483	458	106	2.6k
G. Bernaschek Austria	26	740 0.9×	405 0.8×	360 0.7×	845 1.7×	240 0.5×	159	2.3k
Benjamin Piura Israel	29	640 0.8×	460 0.9×	708 1.4×	226 0.5×	420 0.9×	163	2.9k
Denys W. Fortune Australia	27	583 0.7×	219 0.4×	603 1.2×	476 1.0×	261 0.6×	92	2.1k
B S Mahony United States	25	843 1.0×	153 0.3×	609 1.2×	1.0k 2.1×	315 0.7×	42	2.3k
Vinita Parkash United States	32	444 0.5×	485 1.0×	1.5k 3.0×	261 0.5×	749 1.6×	121	3.0k
Christian Schwentner Germany	30	1.6k 2.0×	731 1.4×	187 0.4×	396 0.8×	869 1.9×	208	3.3k
Yoichi Aoki Japan	27	687 0.8×	358 0.7×	1.4k 2.8×	319 0.7×	280 0.6×	179	2.7k
J.L. Benedet Canada	27	780 1.0×	254 0.5×	1.5k 3.1×	222 0.5×	255 0.6×	56	3.1k
Peter Oppelt United States	31	430 0.5×	431 0.8×	826 1.7×	306 0.6×	479 1.0×	149	2.8k
Yoav H. Messinger United States	32	1.7k 2.1×	844 1.7×	66 0.1×	299 0.6×	1.2k 2.6×	106	3.5k

Countries citing papers authored by Philippe Moerman

Since Specialization

Citations

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

Fields of papers citing papers by Philippe Moerman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philippe Moerman

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

Moerman, Philippe, et al.. (2018). Discordance for placental mesenchymal dysplasia in a monochorionic diamniotic twin pregnancy: A case report. Clinical Case Reports. 6(8). 1557–1560. 9 indexed citations

Moisse, Matthieu, Jeroen Depreeuw, Daniela Annibali, et al.. (2017). Integrated genome analysis of uterine leiomyosarcoma to identify novel driver genes and targetable pathways. International Journal of Cancer. 142(6). 1230–1243. 57 indexed citations

Michielsen, Katrijn, Ignace Vergote, Raphaëla C. Dresen, et al.. (2016). Whole-body diffusion-weighted magnetic resonance imaging in the diagnosis of recurrent ovarian cancer: a clinical feasibility study. British Journal of Radiology. 89(1067). 20160468–20160468. 19 indexed citations

Limbergen, Erik Van, et al.. (2015). Para-aortic lymph node metastases in locally advanced cervical cancer: Comparison between surgical staging and imaging. Gynecologic Oncology. 138(2). 299–303. 41 indexed citations

Michielsen, Katrijn, Ignace Vergote, Katya Op de beeck, et al.. (2013). Whole-body MRI with diffusion-weighted sequence for staging of patients with suspected ovarian cancer: a clinical feasibility study in comparison to CT and FDG-PET/CT. European Radiology. 24(4). 889–901. 162 indexed citations

Leunen, Karin, Olivier Gevaert, Anneleen Daemen, et al.. (2009). Recurrent copy number alterations inBRCA1-mutated ovarian tumors alter biological pathways. Human Mutation. 30(12). 1693–1702. 7 indexed citations

Thienpont, Bernard, Thomy de Ravel, Hilde Van Esch, et al.. (2007). Partial duplications of the ATRX gene cause the ATR-X syndrome. European Journal of Human Genetics. 15(10). 1094–1097. 25 indexed citations

Witters, Ingrid, Mieke Cannie, Philippe Moerman, et al.. (2007). Fetal Caudal Dysgenesis after Maternal Cardiopulmonary Bypass in Pregnancy. Ultrasound. 15(2). 71–72. 2 indexed citations

Moerman, Philippe, et al.. (2006). Second case of uterine mesonephric adenocarcinoma. International Journal of Gynecological Cancer. 16(3). 1450–1454. 23 indexed citations

10.

Breysem, Luc, et al.. (2005). Fetal Magnetic Resonance Imaging of an Intracranial Venous Thrombosis. Fetal Diagnosis and Therapy. 21(1). 13–17. 22 indexed citations

11.

Allegaert, Karel, et al.. (2002). Neonatal transthoracic puncture in a case of congenital cystic adenomatoid malformation of the lung. Journal of Pediatric Surgery. 37(10). 1495–1497. 6 indexed citations

12.

Ayadi, A., Hong Zheng, Peter Sobieszczuk, et al.. (2001). Net-targeted mutant mice develop a vascular phenotype and up-regulate egr-1. The EMBO Journal. 20(18). 5139–5152. 105 indexed citations

13.

Raemdonck, Dirk Van, K. De Boeck, Hugo Devlieger, et al.. (2001). Pulmonary sequestration: a comparison between pediatric and adult patients. European Journal of Cardio-Thoracic Surgery. 19(4). 388–395. 128 indexed citations

14.

Witters, Ingrid, et al.. (2001). Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome. Annales de Génétique. 44(4). 179–182. 24 indexed citations

15.

Cin, Paola Dal, Sylke Wanschura, Bernd Kazmierczak, et al.. (1998). Amplification and expression of the HMGIC gene in a benign endometrial polyp. Genes Chromosomes and Cancer. 22(2). 95–99. 5 indexed citations

16.

Moerman, Philippe, J P Fryns, S H Sastrowijoto, Kamiel Vandenberghe, & Joseph M. Lauweryns. (1994). Hereditary Renal Adysplasia: New Observations and Hypotheses. Pediatric Pathology. 14(3). 405–410. 19 indexed citations

17.

Koninckx, Philippe R., et al.. (1992). CA 125 concentrations in ovarian ‘chocolate’ cyst fluid can differentiate an endometriotic cyst from a cystic corpus luteum. Human Reproduction. 7(9). 1314–1317. 34 indexed citations

18.

Moerman, Philippe, et al.. (1992). Acrofacial dysostosis syndrome type Rodriguez: A new lethal MCA syndrome. American Journal of Medical Genetics. 42(3). 343–345. 15 indexed citations

19.

Moerman, Philippe & Jean‐Pierre Fryns. (1990). The fetal akinesia deformation sequence. A fetopathological approach.. PubMed. 1(1). 25–33. 16 indexed citations

20.

Tricot, Guido, Jean‐Pierre Fryns, José Thomas, et al.. (1983). 5q− anomaly in a patient with disseminated teratoma. Cancer Genetics and Cytogenetics. 9(3). 239–244. 15 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.

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