Patrick Yap

1.3k total citations
9 papers, 186 citations indexed

About

Patrick Yap is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Patrick Yap has authored 9 papers receiving a total of 186 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Patrick Yap's work include Genomics and Rare Diseases (3 papers), Connective tissue disorders research (3 papers) and Cancer Genomics and Diagnostics (2 papers). Patrick Yap is often cited by papers focused on Genomics and Rare Diseases (3 papers), Connective tissue disorders research (3 papers) and Cancer Genomics and Diagnostics (2 papers). Patrick Yap collaborates with scholars based in Australia, United States and New Zealand. Patrick Yap's co-authors include Tiong Yang Tan, Naomi L. Baker, Peter G. Farlie, Ravi Savarirayan, Natasha J. Brown, Toshiaki Tanaka, Hiroshi Suzumura, Yoshinori Tsurusaki, Tomoki Kosho and Hirotomo Saitsu and has published in prestigious journals such as Bone, Clinical Genetics and Pediatric Blood & Cancer.

In The Last Decade

Patrick Yap

9 papers receiving 182 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Patrick Yap Australia	7	131	99	24	20	18	9	186
Clémentine Mahaut France	5	122 0.9×	98 1.0×	38 1.6×	20 1.0×	25 1.4×	5	196
Ewelina Bukowska‐Olech Poland	11	147 1.1×	157 1.6×	23 1.0×	25 1.3×	18 1.0×	41	273
Stefano Petrocchi Italy	8	129 1.0×	84 0.8×	31 1.3×	18 0.9×	16 0.9×	15	236
Anna M. Cueto‐González Spain	7	77 0.6×	127 1.3×	12 0.5×	9 0.5×	15 0.8×	22	186
Juliane Eckhold Germany	8	66 0.5×	116 1.2×	18 0.8×	18 0.9×	8 0.4×	10	202
Laurence Faivre France	6	188 1.4×	117 1.2×	24 1.0×	9 0.5×	9 0.5×	7	252
Nils Koelling United Kingdom	7	92 0.7×	137 1.4×	12 0.5×	32 1.6×	8 0.4×	10	214
Ana Medeira Portugal	10	159 1.2×	176 1.8×	59 2.5×	13 0.7×	20 1.1×	17	300
James Fasham United Kingdom	6	83 0.6×	90 0.9×	18 0.8×	15 0.8×	7 0.4×	10	182
Yannis Duffourd France	7	201 1.5×	125 1.3×	13 0.5×	10 0.5×	9 0.5×	8	266

Countries citing papers authored by Patrick Yap

Since Specialization

Citations

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

Fields of papers citing papers by Patrick Yap

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick Yap

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

All Works

Sort: Min cites: Since: Top N: Style:

9 of 9 papers shown

1.

Savarirayan, Ravi, Julie Hoover‐Fong, Patrick Yap, & Svein O. Fredwall. (2024). New treatments for children with achondroplasia. The Lancet Child & Adolescent Health. 8(4). 301–310. 8 indexed citations

2.

Tan, Natalie B., Rachel Stapleton, Zornitza Stark, et al.. (2020). Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review. Molecular Genetics & Genomic Medicine. 8(11). e1508–e1508. 44 indexed citations

3.

Stapleton, Rachel, Tim Morgan, Ian Hayes, et al.. (2018). A pilot study of exome sequencing in a diverse New Zealand cohort with undiagnosed disorders and cancer. Journal of the Royal Society of New Zealand. 48(4). 262–279. 3 indexed citations

4.

Costantini, Alice, Helena Valta, Nissan Baratang, et al.. (2018). Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with “corner fractures”. Bone. 121. 163–171. 12 indexed citations

5.

Farlie, Peter G., Naomi L. Baker, Patrick Yap, & Tiong Yang Tan. (2016). Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology. Molecular Syndromology. 7(6). 312–321. 34 indexed citations

6.

Yap, Patrick & Ravi Savarirayan. (2016). Emerging targeted drug therapies in skeletal dysplasias. American Journal of Medical Genetics Part A. 170(10). 2596–2604. 8 indexed citations

7.

Yap, Patrick, George McGillivray, Fiona Norris, et al.. (2015). Fetal phenotype of 17q12 microdeletion syndrome: renal echogenicity and congenital diaphragmatic hernia in 2 cases. Prenatal Diagnosis. 35(12). 1265–1267. 11 indexed citations

8.

Miyake, Noriko, Yoshinori Tsurusaki, Eriko Koshimizu, et al.. (2015). Delineation of clinical features in Wiedemann–Steiner syndrome caused by KMT2A mutations. Clinical Genetics. 89(1). 115–119. 60 indexed citations

9.

Yap, Patrick, Leanne Super, Jinyi Qin, et al.. (2015). Congenital Retroperitoneal Teratoma in Neurofibromatosis Type 1. Pediatric Blood & Cancer. 63(4). 706–708. 6 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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