Memnune Yüksel‐Apak

1.2k total citations
25 papers, 740 citations indexed

About

Memnune Yüksel‐Apak is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Memnune Yüksel‐Apak has authored 25 papers receiving a total of 740 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Surgery. Recurrent topics in Memnune Yüksel‐Apak's work include Prenatal Screening and Diagnostics (5 papers), Congenital limb and hand anomalies (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Memnune Yüksel‐Apak is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Congenital limb and hand anomalies (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Memnune Yüksel‐Apak collaborates with scholars based in Türkiye, United States and Switzerland. Memnune Yüksel‐Apak's co-authors include Bernd Wollnik, Zehra Oya Uyguner, Hülya Kayserili, Turgut Tükel, Nermin Başerer, Günter Hafız, Güven Lüleci, Giovanni Neri, F Serville and Wendy P. Robinson and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Neurology and The American Journal of Human Genetics.

In The Last Decade

Memnune Yüksel‐Apak

25 papers receiving 714 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Memnune Yüksel‐Apak Türkiye 14 510 283 131 108 72 25 740
Chia‐Cheng Hung Taiwan 19 310 0.6× 181 0.6× 108 0.8× 146 1.4× 81 1.1× 38 785
Yunbo Qiao China 21 804 1.6× 144 0.5× 134 1.0× 38 0.4× 41 0.6× 49 1.1k
Pierangela Castorina Italy 19 494 1.0× 185 0.7× 187 1.4× 113 1.0× 11 0.2× 35 894
Brice Marcet France 16 653 1.3× 213 0.8× 67 0.5× 33 0.3× 95 1.3× 24 1.2k
Tamar Tenne Israel 11 618 1.2× 227 0.8× 69 0.5× 210 1.9× 87 1.2× 19 1.1k
Edmond G. Lemire Canada 14 240 0.5× 202 0.7× 26 0.2× 76 0.7× 67 0.9× 42 616
Mark Kibschull Canada 21 746 1.5× 126 0.4× 27 0.2× 143 1.3× 57 0.8× 34 1.3k
Nataliya Di Donato Germany 18 463 0.9× 371 1.3× 54 0.4× 157 1.5× 49 0.7× 61 914
Buffy S. Ellsworth United States 14 571 1.1× 345 1.2× 49 0.4× 34 0.3× 47 0.7× 29 937
V Der Kaloustian United States 9 296 0.6× 149 0.5× 60 0.5× 38 0.4× 25 0.3× 14 553

Countries citing papers authored by Memnune Yüksel‐Apak

Since Specialization
Citations

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

Fields of papers citing papers by Memnune Yüksel‐Apak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Memnune Yüksel‐Apak. 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 Memnune Yüksel‐Apak. The network helps show where Memnune Yüksel‐Apak may publish in the future.

Co-authorship network of co-authors of Memnune Yüksel‐Apak

This figure shows the co-authorship network connecting the top 25 collaborators of Memnune Yüksel‐Apak. A scholar is included among the top collaborators of Memnune Yüksel‐Apak 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 Memnune Yüksel‐Apak. Memnune Yüksel‐Apak 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.
Yüksel‐Apak, Memnune, Nina Bögershausen, Barbara Pawlik, et al.. (2012). A large duplication involving the IHH locus mimics acrocallosal syndrome. European Journal of Human Genetics. 20(6). 639–644. 11 indexed citations
2.
Üzümcü, Abdullah, Şükrü Candan, Güven Toksoy, et al.. (2009). Mutational screening of BASP1 and transcribed processed pseudogene TPΨg-BASP1 in patients with Möbius syndrome. Journal of genetics and genomics. 36(4). 251–256. 3 indexed citations
3.
Başaran, Seher, Birsen Karaman, Güven Toksoy, et al.. (2004). The Results of Cytogenetic Analysis with Regard to Intracytoplasmic Sperm Injection in Males, Females and Fetuses. Fetal Diagnosis and Therapy. 19(4). 313–318. 7 indexed citations
4.
Tükel, Turgut, Zehra Oya Uyguner, Ji‐Qing Wei, et al.. (2003). A Novel Semiquantitative Polymerase Chain Reaction/Enzyme Digestion-Based Method for Detection of Large Scale Deletions/Conversions of the CYP21 Gene and Mutation Screening in Turkish Families with 21-Hydroxylase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 88(12). 5893–5897. 37 indexed citations
5.
Maassen, J. A., Edward S. Tobias, Turgut Tükel, et al.. (2003). Identification and Functional Assessment of Novel and Known Insulin Receptor Mutations in Five Patients with Syndromes of Severe Insulin Resistance. The Journal of Clinical Endocrinology & Metabolism. 88(9). 4251–4257. 29 indexed citations
6.
Wollnik, Bernd, et al.. (2003). Homozygous and heterozygous inheritance of PAX3 mutations causes different types of Waardenburg syndrome. American Journal of Medical Genetics Part A. 122A(1). 42–45. 56 indexed citations
7.
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
8.
Uyguner, Zehra Oya, et al.. (2003). Frequencies of gap‐ and tight‐junction mutations in Turkish families with autosomal‐recessive non‐syndromic hearing loss. Clinical Genetics. 64(1). 65–69. 89 indexed citations
9.
Utku, Ufuk, Yahya Çelik, Zehra Oya Uyguner, Memnune Yüksel‐Apak, & Bernd Wollnik. (2002). CADASIL syndrome in a large Turkish kindred caused by the R90C mutation in the Notch3 receptor. European Journal of Neurology. 9(1). 23–28. 27 indexed citations
10.
Savas, Sevtap, Serpil Eraslan, Sibel Kantarci, et al.. (2002). Prenatal prediction of childhood‐onset spinal muscular atrophy (SMA) in Turkish families. Prenatal Diagnosis. 22(8). 703–709. 10 indexed citations
11.
Uyguner, Zehra Oya, Turgut Tükel, Can Baykal, et al.. (2002). The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family. Clinical Genetics. 62(4). 306–309. 60 indexed citations
12.
Wollnik, Bernd, et al.. (2002). Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish family. Ophthalmic Genetics. 23(1). 29–36. 11 indexed citations
13.
Wollnik, Bernd, Hülya Kayserili, Zehra Oya Uyguner, Turgut Tükel, & Memnune Yüksel‐Apak. (2002). Haploinsufficiency of TBX3 causes ulnar-mammary syndrome in a large Turkish family. Annales de Génétique. 45(4). 213–217. 24 indexed citations
14.
Kayserili, Hülya, Timothy C. Cox, Liza L. Cox, et al.. (2001). Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS). Journal of Medical Genetics. 38(6). 411–417. 15 indexed citations
15.
Savas, Sevtap, Nalan Gökgöz, Hülya Kayserili, et al.. (2000). Screening of Deletions in SMN, NAIP and BTF2p44 Genes in Turkish Spinal Muscular Atrophy Patients. Human Heredity. 50(3). 162–165. 11 indexed citations
16.
Çelik, Arzu, Serpil Eraslan, Nalan Gökgöz, et al.. (1997). Identification of the parental origin of polysomy in two 49,XXXXY cases. Clinical Genetics. 51(6). 426–429. 15 indexed citations
17.
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
18.
Oğur, Gönül, et al.. (1994). Clinical, ultrastructural and biochemical studies in two sibs with Ehlers‐Danlos syndrome type VI‐B‐like features. Clinical Genetics. 46(6). 417–422. 8 indexed citations
19.
Gökgöz, Nalan, et al.. (1993). Screening of deletions and RFLP analysis in Turkish DMD/BMD families by PCR. Clinical Genetics. 43(5). 261–266. 13 indexed citations
20.
Oğur, Gönül, Memnune Yüksel‐Apak, & Misten Demiryont. (1990). Syndrome of congenital cutis laxa with ligamentous laxity and delayed development: Report of a brother and sister from Turkey. American Journal of Medical Genetics. 37(1). 6–9. 12 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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