Funda Suer

592 total citations
16 papers, 256 citations indexed

About

Funda Suer is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Funda Suer has authored 16 papers receiving a total of 256 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Funda Suer's work include Genetic Associations and Epidemiology (3 papers), RNA regulation and disease (3 papers) and Hair Growth and Disorders (2 papers). Funda Suer is often cited by papers focused on Genetic Associations and Epidemiology (3 papers), RNA regulation and disease (3 papers) and Hair Growth and Disorders (2 papers). Funda Suer collaborates with scholars based in United States, Türkiye and Ireland. Funda Suer's co-authors include Ahmet Rüçhan Akar, Ali̇ İnal, Ercan Arca, Eric P. Hoffman, Heather Gordish‐Dressman, Metin Özata, Paul M. Gordon, Brennan Harmon, Robert F. Zoeller and Paul S. Visich and has published in prestigious journals such as Journal of Applied Physiology, BMC Genomics and Journal of Cellular Biochemistry.

In The Last Decade

Funda Suer

16 papers receiving 249 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Funda Suer United States	11	84	81	73	49	33	16	256
Inger Pihl-Lundin Sweden	9	84 1.0×	49 0.6×	81 1.1×	127 2.6×	64 1.9×	12	377
Elena Piozzi Italy	11	81 1.0×	33 0.4×	47 0.6×	8 0.2×	26 0.8×	26	373
M. Apostolakis Germany	9	64 0.8×	38 0.5×	34 0.5×	21 0.4×	39 1.2×	56	298
Marc Michel United States	7	146 1.7×	24 0.3×	53 0.7×	21 0.4×	33 1.0×	14	346
Justin Jacobse Netherlands	10	65 0.8×	45 0.6×	9 0.1×	90 1.8×	36 1.1×	24	318
Feifei Cui China	8	76 0.9×	12 0.1×	25 0.3×	69 1.4×	25 0.8×	19	305
Noha Ahmed Egypt	4	91 1.1×	10 0.1×	21 0.3×	51 1.0×	29 0.9×	8	269
Pirkko Saarinen Finland	8	57 0.7×	32 0.4×	16 0.2×	11 0.2×	21 0.6×	20	389
Josep Calafell-Segura Spain	16	130 1.5×	67 0.8×	22 0.3×	71 1.4×	10 0.3×	32	563
H Beck Denmark	9	33 0.4×	38 0.5×	27 0.4×	115 2.3×	35 1.1×	32	332

Countries citing papers authored by Funda Suer

Since Specialization

Citations

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

Fields of papers citing papers by Funda Suer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Funda Suer

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

All Works

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16 of 16 papers shown

Katz, M., et al.. (2025). Patient perspectives after receiving simulated preconception polygenic risk scores (PRS) for family planning. Journal of Assisted Reproduction and Genetics. 42(3). 997–1013. 2 indexed citations

Schreiber‐Agus, Nicole, Xiaoqiang Cai, Guiqing Cai, et al.. (2019). Lessons learned from expanded reproductive carrier screening in self‐reported Ashkenazi, Sephardi, and Mizrahi Jewish patients. Molecular Genetics & Genomic Medicine. 8(2). e1053–e1053. 12 indexed citations

Suer, Funda, Arthur F. Harralson, David Frankfurter, Paul R. Gindoff, & Travis J. O’Brien. (2015). Targeted single molecule sequencing methodology for ovarian hyperstimulation syndrome. BMC Genomics. 16(1). 264–264. 8 indexed citations

O’Brien, Travis J., et al.. (2014). Kinase insert domain receptor/vascular endothelial growth factor receptor 2 (KDR) genetic variation is associated with ovarian hyperstimulation syndrome. Reproductive Biology and Endocrinology. 12(1). 36–36. 6 indexed citations

Devaney, Joseph M., Paul D. Thompson, Paul S. Visich, et al.. (2011). The 1p13.3 LDL (C)-Associated Locus Shows Large Effect Sizes in Young Populations. Pediatric Research. 69(6). 538–543. 13 indexed citations

Suer, Funda, Brennan Harmon, Heather Gordish‐Dressman, et al.. (2010). MC4R Variant Is Associated With BMI but Not Response to Resistance Training in Young Females. Obesity. 19(3). 662–666. 16 indexed citations

Harmon, Brennan, Funda Suer, Heather Gordish‐Dressman, et al.. (2010). CCL2 and CCR2 variants are associated with skeletal muscle strength and change in strength with resistance training. Journal of Applied Physiology. 109(6). 1779–1785. 31 indexed citations

Devaney, Joseph M., Laura L. Tosi, David T. Fritz, et al.. (2009). Differences in fat and muscle mass associated with a functional human polymorphism in a post‐transcriptional BMP2 gene regulatory element. Journal of Cellular Biochemistry. 107(6). 1073–1082. 30 indexed citations

Suer, Funda, Heather Gordish‐Dressman, Priscilla M. Clarkson, et al.. (2008). INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men. BMC Medical Genetics. 9(1). 117–117. 23 indexed citations

10.

Altun, Ceyhan, et al.. (2008). Human leukocyte antigen class II alleles and dental caries in a child population.. PubMed. 30(2). 154–9. 9 indexed citations

11.

Akar, Ahmet, et al.. (2007). Vitamin D receptor gene polymorphisms are not associated with alopecia areata. International Journal of Dermatology. 46(9). 927–929. 15 indexed citations

12.

Suer, Funda, et al.. (2005). The vitamin D receptor fokl start codon polymorphism and bone mineral density in male hypogonadotrophic hypogonadism. Journal of Endocrinological Investigation. 28(11). 810–814. 2 indexed citations

13.

Suer, Funda, Hatice Mergen, Erol Bolu, & Metin Özata. (2005). Molecular Scanning for Mutations in the Insulin Receptor Substrate-1 (Irs-1) Gene in Turkish with Type 2 Diabetes Mellitus. Endocrine Journal. 52(5). 593–598. 21 indexed citations

14.

Akdemir, Ramazan, Hakan Özhan, Enver Erbilen, et al.. (2004). HLA-DR B1 and DQ B1 polymorphisms in patients with coronary artery ectasia. Acta Cardiologica. 59(5). 499–502. 10 indexed citations

15.

Akar, Ahmet Rüçhan, et al.. (2004). Association of HLA Class I Antigens and HLA Class II Alleles with Vitiligo in a Turkish Population. Pigment Cell Research. 17(2). 181–184. 48 indexed citations

16.

Akar, Ahmet Rüçhan, et al.. (2004). Lack of association between Vitamin D receptor FokI polymorphism and alopecia areata.. PubMed. 14(3). 156–8. 10 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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