Aytemiz Gürgey

5.2k total citations
219 papers, 3.9k citations indexed

About

Aytemiz Gürgey is a scholar working on Hematology, Genetics and Physiology. According to data from OpenAlex, Aytemiz Gürgey has authored 219 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 141 papers in Hematology, 90 papers in Genetics and 32 papers in Physiology. Recurrent topics in Aytemiz Gürgey's work include Hemoglobinopathies and Related Disorders (66 papers), Blood Coagulation and Thrombosis Mechanisms (47 papers) and Iron Metabolism and Disorders (39 papers). Aytemiz Gürgey is often cited by papers focused on Hemoglobinopathies and Related Disorders (66 papers), Blood Coagulation and Thrombosis Mechanisms (47 papers) and Iron Metabolism and Disorders (39 papers). Aytemiz Gürgey collaborates with scholars based in Türkiye, United States and France. Aytemiz Gürgey's co-authors include Çiğdem Altay, Fatma Gümrük, Günay Balta, F. Kutlar, L. Mesci, Deniz Aslan, C Altay, Abdullah Kutlar, Gönül Hiçsönmez and R. Öner and has published in prestigious journals such as Cell, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Aytemiz Gürgey

212 papers receiving 3.7k citations

Peers

Countries citing papers authored by Aytemiz Gürgey

Since Specialization

Citations

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

Fields of papers citing papers by Aytemiz Gürgey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aytemiz Gürgey

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

#	Work	Indexed citations
1	PARVOVIRUS B19-INDUCED PERSISTENT PURE RED CELL APLASIA IN A CHILD WITH T-CELL IMMUNODEFICIENCY 2009 ·Pediatric Hematology and Oncology ·Betül Tavil, Özden Sanal, Tuba Turul, Leman Yel, Aytemiz Gürgey, Fatma Gümrük	7
2	Nonstroke arterial thrombosis in children: Hacettepe experience 2008 ·Blood Coagulation & Fibrinolysis ·Yasemin Işık Balcı, Şule Ünal, Fatma Gümrük, Mualla Çetin, Süheyla Özkutlu, Aytemiz Gürgey	3
3	Familial pulmonary arterial hypertension, leucopenia, and atrial septal defect: a probable new familial syndrome with multisystem involvement 2008 ·Clinical Dysmorphology ·Ali Dursun, Rıza Köksal Özgül, (unknown), (unknown), Aytemiz Gürgey, Alpay Çeliker, Robyn J. Barst, James A. Knowles, (unknown), Jane H. Morse	16
4	Natural history and early diagnosis of LAD-1/variant syndrome 2006 ·Blood ·Taco W. Kuijpers, Robin van Bruggen, Nanne M. Kamerbeek, Anton T. J. Tool, Gönül Hiçsönmez, Aytemiz Gürgey, Axel Karow, Arthur J. Verhoeven, Karl Seeger, Özden Sanal, Charlotte M. Niemeyer, Dirk Roos	76
5	PROTHROMBIN G20210A MUTATION IN TURKISH CHILDREN WITH THROMBOSIS AND THE FREQUENCY OF PROTHROMBIN C20209T 2005 ·Pediatric Hematology and Oncology ·Aytemiz Gürgey, Selma Ünal, Hamza Okur, Feride Duru, Fatma Gümrük	9
6	Symptomatic Thrombosis in Turkish Neonates 2004 ·Journal of Pediatric Hematology/Oncology ·Aytemiz Gürgey, Gülsevin Tekinalp, (unknown), (unknown)	6
7	Factor V Leiden mutation and PAI-1 gene 4G/5G genotype in thrombotic patients with Behcet's disease 2003 ·Blood Coagulation & Fibrinolysis ·Aytemiz Gürgey, Günay Balta, Ayşe Boyvat	26
8	THROMBOCYTOPENIA AND EMPERIPOLESIS IN A PATIENT WITH HEPATITIS A INFECTION 2002 ·Pediatric Hematology and Oncology ·Zekai Avcı, Tuba Turul, Ferhat Çatal, Şeref Olgar, Ali Baykan, Özlem Tekşam, Aytemiz Gürgey	14
9	LOW SERUM CARNITINE CONCENTRATIONS IN HEALTHY CHILDREN WITH IRON DEFICIENCY ANEMIA 2001 ·Pediatric Hematology and Oncology ·Ayşe Pínar Cemeroğlu, Coşkun Kocabaş, Turgay Coşkun, Aytemiz Gürgey	5
10	HOMOZYGOSITY FOR Hb E-SASKATOON [β22(B4)Glu → Lys] IN A TURKISH PATIENT 2001 ·Hemoglobin ·Esra Birben, R. Öner, Cihan Öner, Fatma Gümrük, Aytemiz Gürgey, Çiğdem Altay	8
11	A case of hemophilia A associated with Hodgkin's disease. 2000 ·PubMed ·Ahmet Koç, Ali Varan, Münevver Büyükpamukçu, Aytemiz Gürgey	1
12	The relative levels of α2-, α1-, and ζ-mRNA in HB H patients with different deletional and nondeletional α-thalassemia determinants 1996 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Н.С. Сметанина, Cihan Öner, E. Baysal, R. Öner, (unknown), Çiğdem Altay, Aytemiz Gürgey, Adekunle Adekile, (unknown), T. H. J. Huisman	6
13	Factor V Q 506 mutation in children with thrombosis 1996 ·American Journal of Hematology ·Aytemiz Gürgey, L. Mesci, Yavuz Renda, Lale Olcay, Nurten Koçak, Gülşen Erdem	44
14	Hb adana or α₂59(E8)Gly→Aspβ₂, A severely unstable α₁‐globin variant, observed in combination with the ‐(α)20.5 KB α‐thal‐1 deletion in two Turkish patients 1993 ·American Journal of Hematology ·Mehmet Akif Çürük, Aleksandar Dimovski, E. Baysal, (unknown), F. Kutlar, T. P. Molchanova, B. B. Webber, Çiğdem Altay, Aytemiz Gürgey, T. H. J. Huisman	64
15	Pearson’s Marrow-Pancreas Syndrome in 2 Turkish Children 1992 ·Acta Haematologica ·Aytemiz Gürgey, Agnès Rötig, Fatma Gümrük, (unknown), (unknown), Çiğdem Altay	9
16	High remission rate in acute myeloblastic leukemia in children treated with high‐dose methylprednisolone 1992 ·European Journal Of Haematology ·Gönül Hiçsönmez, (unknown), (unknown), A. Murat Tuncer, Fatma Gümrük, (unknown), Aytemiz Gürgey, Şînasi Özsoylu	18
17	Hydrops fetalis due to Homozygosity for α-Thalassemia-1, -(α)-20.5 kb: The First Observation in a Turkish Family 1989 ·Acta Haematologica ·Aytemiz Gürgey, Çiğdem Altay, Mehmet Sinan Beksaç, (unknown), F. Kutlar, T. H. J. Huisman	14
18	Homozygosity for hemoglobin O-Arab (alpha 2 beta 2 121 Glu----Lys). Hb O-Arab disease. 1986 ·PubMed ·Çiğdem Altay, Aytemiz Gürgey, Huisman Th	3
19	An ultrastructural study in a case of Wolman's disease (clinical, biochemical, light and electron microscopic study). 1978 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·Yavuz Özoran, (unknown), (unknown), Aytemiz Gürgey, Şînasi Özsoylu, Nadir Koçak, G Ciliv	1
20	Wolman's disease. A case report with lipid, chromosome and electronmicroscopic studies. 1977 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·Şînasi Özsoylu, Aytemiz Gürgey, Nadir Koçak, Yavuz Özoran, (unknown), (unknown), G Ciliv	1

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