H. Ermiş

415 total citations
23 papers, 290 citations indexed

About

H. Ermiş is a scholar working on Pediatrics, Perinatology and Child Health, Infectious Diseases and Pathology and Forensic Medicine. According to data from OpenAlex, H. Ermiş has authored 23 papers receiving a total of 290 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Pediatrics, Perinatology and Child Health, 5 papers in Infectious Diseases and 4 papers in Pathology and Forensic Medicine. Recurrent topics in H. Ermiş's work include Prenatal Screening and Diagnostics (15 papers), Parvovirus B19 Infection Studies (5 papers) and Fetal and Pediatric Neurological Disorders (4 papers). H. Ermiş is often cited by papers focused on Prenatal Screening and Diagnostics (15 papers), Parvovirus B19 Infection Studies (5 papers) and Fetal and Pediatric Neurological Disorders (4 papers). H. Ermiş collaborates with scholars based in Türkiye and Germany. H. Ermiş's co-authors include İbrahim Kalelioğlu, Recep Has, L. İbrahimoğlu, Tuba Günel, Kılıç Aydinli, Seher Başaran, Atıl Yüksel, Pınar Akçakaya, Ali Benian and Cem Batukan and has published in prestigious journals such as Ultrasound in Obstetrics and Gynecology, BMC Pregnancy and Childbirth and American Journal of Medical Genetics.

In The Last Decade

H. Ermiş

23 papers receiving 279 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H. Ermiş Türkiye 9 170 102 69 56 56 23 290
Ahmad El-Sheikhah Egypt 10 349 2.1× 123 1.2× 32 0.5× 73 1.3× 64 1.1× 14 454
Chanwei Jia China 12 68 0.4× 50 0.5× 46 0.7× 87 1.6× 108 1.9× 19 343
Monique A. M. Mulders Netherlands 10 236 1.4× 100 1.0× 48 0.7× 99 1.8× 27 0.5× 14 309
Simona De Toffol Italy 11 303 1.8× 46 0.5× 22 0.3× 84 1.5× 51 0.9× 15 412
Oshrit Lebovitz Israel 12 117 0.7× 212 2.1× 12 0.2× 60 1.1× 170 3.0× 26 488
Evan M. Rosenbluth United States 6 127 0.7× 61 0.6× 129 1.9× 132 2.4× 190 3.4× 8 377
M. Meijer‐Hoogeveen Netherlands 13 348 2.0× 74 0.7× 12 0.2× 67 1.2× 222 4.0× 14 521
Maria Carla Pittalis Italy 13 419 2.5× 57 0.6× 16 0.2× 132 2.4× 68 1.2× 26 564
V. H. W. M. Jongen Netherlands 10 38 0.2× 213 2.1× 36 0.5× 50 0.9× 86 1.5× 21 415
M Mincheva United Kingdom 5 77 0.5× 31 0.3× 39 0.6× 89 1.6× 81 1.4× 16 246

Countries citing papers authored by H. Ermiş

Since Specialization
Citations

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

Fields of papers citing papers by H. Ermiş

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Ermiş

This figure shows the co-authorship network connecting the top 25 collaborators of H. Ermiş. A scholar is included among the top collaborators of H. Ermiş 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 H. Ermiş. H. Ermiş 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.
Günel, Tuba, Mohammad Kazem Hosseini, İbrahim Kalelioğlu, et al.. (2014). Current approaches on non-invasive prenatal diagnosis: Prenatal genomics, transcriptomics, personalized fetal diagnosis. Journal of Turkish Society of Obstetric and Gynecology. 11(4). 233–241. 3 indexed citations
2.
Has, Recep, İbrahim Kalelioğlu, Aytül Çorbacıoğlu Esmer, et al.. (2014). Bipolar Cord Coagulation in the Management of Complicated Monochorionic Twin Pregnancies. Fetal Diagnosis and Therapy. 36(3). 190–195. 15 indexed citations
3.
Has, Recep, İbrahim Kalelioğlu, Aytül Çorbacıoğlu Esmer, et al.. (2014). Stage-Related Outcome after Fetoscopic Laser Ablation in Twin-to-Twin Transfusion Syndrome. Fetal Diagnosis and Therapy. 36(4). 287–292. 15 indexed citations
4.
Günel, Tuba, İbrahim Kalelioğlu, H. Ermiş, Recep Has, & Kılıç Aydinli. (2012). Large Scale Pre-Diagnosis ofToxoplasma GondiiDNA Genotyping by Real-Time PCR on Amniotic Fluid. Biotechnology & Biotechnological Equipment. 26(2). 2913–2915. 6 indexed citations
5.
Günel, Tuba, İbrahim Kalelioğlu, Ali Gedikbaşı, H. Ermiş, & Kılıç Aydinli. (2011). Detection of fetal RHD pseudogene (RHDΨ) and hybrid RHD-CE-Ds from RHD-negative pregnant women with a free DNA fetal kit. Genetics and Molecular Research. 10(4). 2653–2657. 5 indexed citations
6.
Günel, Tuba, Pınar Akçakaya, İbrahim Kalelioğlu, et al.. (2011). Serum microRNA expression in pregnancies with preeclampsia. Genetics and Molecular Research. 10(4). 4034–4040. 81 indexed citations
7.
Günel, Tuba, et al.. (2011). Comparison of real-time polymerase chain reaction assay methods for detection of RHD gene in amniotic fluid. Journal of Natural Science Biology and Medicine. 2(2). 193–193. 5 indexed citations
8.
Günel, Tuba, İbrahim Kalelioğlu, H. Ermiş, & Kılıç Aydinli. (2010). Detection of fetal RhD gene from maternal blood. Journal of the Turkish-German Gynecological Association. 11(2). 82–85. 6 indexed citations
9.
Has, Recep, et al.. (2008). Fetal Nasal Bone Assessment in First Trimester Down Syndrome Screening. Fetal Diagnosis and Therapy. 24(1). 61–66. 13 indexed citations
10.
Has, Recep, İbrahim Kalelioğlu, H. Ermiş, et al.. (2006). Screening for Fetal Chromosomal Abnormalities with Nuchal Translucency Measurement in the First Trimester. Fetal Diagnosis and Therapy. 21(4). 355–359. 8 indexed citations
11.
Has, Recep, et al.. (2004). Therapeutic amniocentesis for treatment of twin–twin transfusion syndrome. Archives of Gynecology and Obstetrics. 271(1). 22–25. 3 indexed citations
12.
Has, Recep, et al.. (2004). Dandy-Walker Malformation: A Review of 78 Cases Diagnosed by Prenatal Sonography. Fetal Diagnosis and Therapy. 19(4). 342–347. 39 indexed citations
13.
Aslan, Halıl, et al.. (2003). Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity. BMC Pregnancy and Childbirth. 3(1). 1–1. 22 indexed citations
14.
Karaman, Birsen, Bernd Wollnik, H. Ermiş, Memnune Yüksel‐Apak, & Seher Başaran. (2003). A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish family. Prenatal Diagnosis. 23(4). 336–339. 3 indexed citations
15.
Has, Recep, et al.. (2002). Partial Molar Appearance of the Placenta in Trisomy 13. Fetal Diagnosis and Therapy. 17(4). 205–208. 9 indexed citations
16.
Tercanli, Sevgi, et al.. (2002). Nackentransparenzscreening im 1. Trimenon: Ergebnisse einer prospektiven Studie bei 1980 Feten aus einem Zentrum in der Schweiz. Ultraschall in der Medizin - European Journal of Ultrasound. 23(1). 22–26. 5 indexed citations
17.
Has, Recep, Cem Batukan, H. Ermiş, et al.. (2002). Comparison of 25 and 50 μg Vaginally Administered Misoprostol for Preinduction of Cervical Ripening and Labor Induction. Gynecologic and Obstetric Investigation. 53(1). 16–21. 20 indexed citations
18.
Has, Recep, et al.. (2000). A malformed fetus in a rudimentary uterine horn pregnancy. Ultrasound in Obstetrics and Gynecology. 16(2). 200–202. 3 indexed citations
19.
Has, Recep, et al.. (2000). A 22-Week Cervical Pregnancy. Gynecologic and Obstetric Investigation. 50(2). 139–141. 6 indexed citations
20.
Başaran, Seher, et al.. (1994). Tetra‐amelia, lung hypo‐/aplasia, cleft lip‐palate, and heart defect: A new syndrome?. American Journal of Medical Genetics. 51(1). 77–80. 18 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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