Ph. Moerman

1.4k total citations
43 papers, 856 citations indexed

About

Ph. Moerman is a scholar working on Surgery, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Ph. Moerman has authored 43 papers receiving a total of 856 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Surgery, 11 papers in Pediatrics, Perinatology and Child Health and 11 papers in Genetics. Recurrent topics in Ph. Moerman's work include Congenital Diaphragmatic Hernia Studies (9 papers), Congenital Anomalies and Fetal Surgery (7 papers) and Ovarian cancer diagnosis and treatment (5 papers). Ph. Moerman is often cited by papers focused on Congenital Diaphragmatic Hernia Studies (9 papers), Congenital Anomalies and Fetal Surgery (7 papers) and Ovarian cancer diagnosis and treatment (5 papers). Ph. Moerman collaborates with scholars based in Belgium, United States and Netherlands. Ph. Moerman's co-authors include J. P. Fryns, Frédéric Amant, P. Goddeeris, Joseph M. Lauweryns, Ingrid Witters, Karin Leunen, J. P. Fryns, Dominique Van Schoubroeck, I. Vergote and D. Timmerman and has published in prestigious journals such as The Lancet, British Journal of Cancer and European Respiratory Journal.

In The Last Decade

Ph. Moerman

43 papers receiving 822 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ph. Moerman Belgium 19 294 178 176 174 172 43 856
Maija‐Riitta Ordén Finland 13 125 0.4× 194 1.1× 55 0.3× 153 0.9× 100 0.6× 22 572
Takafumi Fujino Japan 16 215 0.7× 221 1.2× 135 0.8× 96 0.6× 374 2.2× 37 1.0k
Yaron Zalel Israel 24 350 1.2× 103 0.6× 206 1.2× 577 3.3× 365 2.1× 62 1.4k
Murray Joseph Casey United States 17 177 0.6× 155 0.9× 284 1.6× 41 0.2× 401 2.3× 43 939
M S Golbus United States 17 337 1.1× 140 0.8× 186 1.1× 685 3.9× 35 0.2× 37 1.1k
Fredrick J. Montz United States 18 569 1.9× 204 1.1× 155 0.9× 90 0.5× 874 5.1× 28 1.7k
K. Hata Japan 17 115 0.4× 162 0.9× 31 0.2× 278 1.6× 259 1.5× 45 821
L Koulischer Belgium 19 154 0.5× 276 1.6× 386 2.2× 208 1.2× 57 0.3× 94 1.1k
Ashutosh Halder India 16 121 0.4× 194 1.1× 166 0.9× 243 1.4× 110 0.6× 84 684
S. Kertschanska Germany 12 91 0.3× 91 0.5× 47 0.3× 249 1.4× 45 0.3× 16 641

Countries citing papers authored by Ph. Moerman

Since Specialization
Citations

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

Fields of papers citing papers by Ph. Moerman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ph. Moerman

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

All Works

20 of 20 papers shown
1.
2.
Vandorpe, T., Ann Smeets, Ben Van Calster, et al.. (2011). Lobular and non-lobular breast cancers differ regarding axillary lymph node metastasis: a cross-sectional study on 4,292 consecutive patients. Breast Cancer Research and Treatment. 128(2). 429–435. 27 indexed citations
3.
Cannie, Mieke, Carmela Votino, Ph. Moerman, et al.. (2011). Acceptance, reliability and confidence of diagnosis of fetal and neonatal virtuopsy compared with conventional autopsy: a prospective study. Ultrasound in Obstetrics and Gynecology. 39(6). 659–665. 78 indexed citations
4.
Holsbeke, C. Van, et al.. (2009). Hyperreactio luteinalis in a spontaneously conceived singleton pregnancy. Ultrasound in Obstetrics and Gynecology. 33(3). 371–373. 22 indexed citations
5.
Witters, Ingrid, et al.. (2002). MCA syndrome with renal‐hepatic‐pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and Müllerian duct anomalies. American Journal of Medical Genetics. 107(3). 233–236. 2 indexed citations
6.
Witters, Ingrid, Eric Legius, Ph. Moerman, et al.. (2001). Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic hernia. American Journal of Medical Genetics. 103(4). 278–282. 86 indexed citations
7.
Witters, Ingrid, et al.. (2001). Bilateral tibial agenesis with ectrodactyly (OMIM 119100): Further evidence for autosomal recessive inheritance. American Journal of Medical Genetics. 104(3). 209–213. 13 indexed citations
8.
Naulaers, Gunnar, et al.. (2000). Right Diaphragmatic Eventration Associated with Intralobar Pulmonary Sequestration: A Case Report. European Journal of Pediatric Surgery. 10(2). 140–141. 4 indexed citations
9.
Thomeer, Michiel, et al.. (1999). Systemic lupus erythematosus, eosinophilia and Löffler′s endocarditis. An unusual association. European Respiratory Journal. 13(4). 930–930. 14 indexed citations
10.
Lammens, Martin, et al.. (1998). Neuropathological findings in Moebius syndrome. Clinical Genetics. 54(2). 136–141. 25 indexed citations
11.
Devriendt, Koenraad, H. Devlieger, Marc Gewillig, et al.. (1997). Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father Clinical variability of 22q11 deletion. Clinical Genetics. 51(4). 246–249. 22 indexed citations
12.
Moerman, Ph., et al.. (1996). Placental site nodule of the uterine cervix. Histopathology. 29(4). 379–382. 11 indexed citations
13.
Petit, P., Ph. Moerman, & J P Fryns. (1992). Full 69,XXY triploidy and sex‐reversal: a further example of true hermaphrodism associated with multiple malformations. Clinical Genetics. 41(4). 175–177. 5 indexed citations
14.
Petit, P., et al.. (1991). Abdominal distension as the first echographic sign of hydrometrocolpos in a female fetus. European Journal of Obstetrics & Gynecology and Reproductive Biology. 39(2). 99–101. 3 indexed citations
15.
Dyck, Maria Van, et al.. (1989). Idiopathic infantile arterial calcification with cardiac, renal and central nervous system involvement. European Journal of Pediatrics. 148(4). 374–377. 36 indexed citations
16.
Legius, Eric, Ph. Moerman, J. P. Fryns, et al.. (1988). Holzgreve‐Wagner‐Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observation. American Journal of Medical Genetics. 31(2). 269–272. 9 indexed citations
17.
Petit, P., M. Bossens, Debby Thomas, et al.. (1987). Type III congenital cystic adenomatoid malformation of the lung: another cause of elevated alpha fetoprotein?. Clinical Genetics. 32(3). 172–174. 6 indexed citations
18.
Moerman, Ph., B. Van Damme, Willem Proesmans, et al.. (1984). Oligomeganephronic renal hypoplasia in two siblings. The Journal of Pediatrics. 105(1). 75–77. 10 indexed citations
19.
Moerman, Ph., J. P. Fryns, P. Goddeeris, & Joseph M. Lauweryns. (1983). Multiple ankyloses, facial anomalies, and pulmonary hypoplasia associated with severe antenatal spinal muscular atrophy. The Journal of Pediatrics. 103(2). 238–241. 35 indexed citations
20.
Devlieger, H., J. Jaeken, P. Goddeeris, et al.. (1982). Liver necrosis in the new-born infant: Analysis of some precipitating factors in neonatal care. European Journal of Pediatrics. 138(2). 113–119. 8 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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