Muhterem Bahçe

1.4k total citations
34 papers, 898 citations indexed

About

Muhterem Bahçe is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Muhterem Bahçe has authored 34 papers receiving a total of 898 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 13 papers in Pediatrics, Perinatology and Child Health and 7 papers in Molecular Biology. Recurrent topics in Muhterem Bahçe's work include Prenatal Screening and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (9 papers) and Assisted Reproductive Technology and Twin Pregnancy (4 papers). Muhterem Bahçe is often cited by papers focused on Prenatal Screening and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (9 papers) and Assisted Reproductive Technology and Twin Pregnancy (4 papers). Muhterem Bahçe collaborates with scholars based in Türkiye, Serbia and United States. Muhterem Bahçe's co-authors include S. Munné, Carmen Márquez, Jacques Cohen, M. Sandalinas, Larry E. Morrison, M. Cristina Magli, Mona S. Legator, Luca Gianaroli, John J. Fung and Semra Kahraman and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Reproduction and Fertility and Sterility.

In The Last Decade

Muhterem Bahçe

28 papers receiving 844 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Muhterem Bahçe Türkiye 11 711 423 281 171 116 34 898
J. Fischer United States 9 714 1.0× 315 0.7× 320 1.1× 145 0.8× 115 1.0× 18 829
Sara Bono Italy 12 1.1k 1.5× 554 1.3× 357 1.3× 229 1.3× 108 0.9× 17 1.2k
Anıl Biricik Italy 18 1.2k 1.7× 614 1.5× 468 1.7× 315 1.8× 182 1.6× 41 1.5k
Elvire Van Assche Belgium 11 665 0.9× 330 0.8× 543 1.9× 169 1.0× 509 4.4× 12 1.1k
Ettore Cotroneo Italy 8 511 0.7× 226 0.5× 204 0.7× 137 0.8× 63 0.5× 13 635
Norio Miharu Japan 15 459 0.6× 292 0.7× 168 0.6× 159 0.9× 195 1.7× 27 717
Andrea Nuccitelli Italy 10 446 0.6× 256 0.6× 104 0.4× 104 0.6× 28 0.2× 16 593
Maria Carla Pittalis Italy 13 419 0.6× 254 0.6× 68 0.2× 132 0.8× 22 0.2× 26 564
Caixia Lei China 13 231 0.3× 169 0.4× 80 0.3× 104 0.6× 53 0.5× 34 436
M. Meijer‐Hoogeveen Netherlands 13 348 0.5× 171 0.4× 222 0.8× 67 0.4× 143 1.2× 14 521

Countries citing papers authored by Muhterem Bahçe

Since Specialization
Citations

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

Fields of papers citing papers by Muhterem Bahçe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Muhterem Bahçe

This figure shows the co-authorship network connecting the top 25 collaborators of Muhterem Bahçe. A scholar is included among the top collaborators of Muhterem Bahçe 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 Muhterem Bahçe. Muhterem Bahçe 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.
Torun, Deniz, Oral Nevruz, Mesut Akyol, et al.. (2013). Methylation of SOCS3 in Myeloproliferative Neoplasms and Secondary Erythrocytosis/Thrombocythemia. SHILAP Revista de lepidopterología. 30(1). 13–18. 3 indexed citations
3.
Rosti, Rasim Özgür, Kadri Karaer, Birsen Karaman, et al.. (2013). Gorlin–chaudhry–moss syndrome revisited: Expanding the phenotype. American Journal of Medical Genetics Part A. 161(7). 1737–1742. 8 indexed citations
4.
Karaer, Kadri, Rasim Özgür Rosti, Deniz Torun, et al.. (2011). A case with oto-spondylo-mega-epiphyseal-dysplasia (OSMED): the clinical recognition and differential diagnosis.. PubMed. 53(3). 346–51. 2 indexed citations
5.
Torun, Deniz, et al.. (2010). Psikomotor gerilik ile refere edilen bir olguda saptanan marker kromozom ve klinik bulgularla korelasyonu. Cumhuriyet Tıp Dergisi/Cumhuriyet Üniversitesi Tıp Fakültesi dergisi. 32(2). 247–250.
6.
Koç, Altuğ, Şefık Güran, & Muhterem Bahçe. (2010). The progeny of homozygous identical reciprocal translocation carrier mother. American Journal of Medical Genetics Part A. 152A(11). 2886–2887.
7.
Soysal, Yasemin, Muhterem Bahçe, M. Cengiz Yakıcıer, Ahmet İfran, & A. Emin Kürekçi. (2009). Lösemilerin Genetik Tanısında Sitogenetik ve Floresan In Situ Hibridizasyon Yöntemlerinin Etkinliğinin Değerlendirilmesi. DergiPark (Istanbul University).
8.
Güran, Şefık, Muhterem Bahçe, Kürşat Kaptan, et al.. (2009). JAK2 V617F mutation in cases with chronic myeloproliferative disorders and myelodysplastic syndrome. 51(3). 137–140. 1 indexed citations
9.
Güran, Şefık, Deniz Torun, Fatih Mehmet Mutlu, et al.. (2009). A New Syndrome Associated with Absence of Lower Lid Lacrimal Punctum, Ptosis, Elevation Deficiency of Both Eyes and Mild Facial Dysmorphism. Ophthalmic Genetics. 30(3). 146–151. 2 indexed citations
10.
11.
Özbülbül, Nilgün Işıksalan, et al.. (2006). All-trans-retinoic acid-induced myositis in a child with acute promyelocytic leukemia.. PubMed. 91(8 Suppl). ECR35–ECR35. 9 indexed citations
12.
Dinç, Ayhan, Hakan Erdem, Dorota Rowczenio, et al.. (2005). Autosomal dominant periodic fever with AA amyloidosis: Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Turkish family. Journal of Nephrology. 18(5). 626–629. 9 indexed citations
13.
Ural, Ali Uğur, Ferit Avcu, Mahmut İlker Yılmaz, et al.. (2005). Development of Squamous Cell Carcinoma of the Tongue during Induction Chemotherapy for Acute Myeloid Leukemia. Tumori Journal. 91(1). 81–83. 1 indexed citations
14.
Bahçe, Muhterem, et al.. (2004). Partial trisomy 18q11.2→qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization. Annales de Génétique. 47(4). 393–398. 1 indexed citations
15.
Munné, S., Muhterem Bahçe, M. Sandalinas, et al.. (2004). Differences in chromosome susceptibility to aneuploidy and survival to first trimester. Reproductive BioMedicine Online. 8(1). 81–90. 97 indexed citations
16.
Márquez, Carmen, et al.. (2000). Chromosome abnormalities in 1255 cleavage-stage human embryos. Reproductive BioMedicine Online. 1(1). 17–26. 160 indexed citations
17.
Munné, S., Larry E. Morrison, Jingly Fung, et al.. (1998). Spontaneous Abortions Are Reduced After Preconception Diagnosis of Translocations. Journal of Assisted Reproduction and Genetics. 15(5). 290–296. 121 indexed citations
18.
Munné, S., M. Cristina Magli, Muhterem Bahçe, et al.. (1998). Preimplantation diagnosis of the aneuploidies most commonly found in spontaneous abortions and live births: XY, 13, 14, 15, 16, 18, 21, 22. Prenatal Diagnosis. 18(13). 1459–1466. 177 indexed citations
19.
Güran, Şefık, Muhterem Bahçe, Cenǵiz Beyan, Kemal Korkmaz, & S. Yalçin. (1998). P53, p15INK4B, p16INK4A and p57KIP2 mutations during the progression of chronic myeloid leukemia.. PubMed. 29(3). 181–93. 15 indexed citations
20.
Oğur, Gönül, Samim Özen, Necat İmirzalıoğlu, et al.. (1997). Application of the ‘Apt test’ in Prenatal Diagnosis to evaluate the Fetal Origin of Blood obtained by Cordocentesis: results of 30 pregnancies. Prenatal Diagnosis. 17(9). 879–882. 7 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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