Joan Atkin

2.1k total citations
19 papers, 776 citations indexed

About

Joan Atkin is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Joan Atkin has authored 19 papers receiving a total of 776 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Joan Atkin's work include Prenatal Screening and Diagnostics (5 papers), Epigenetics and DNA Methylation (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Joan Atkin is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Epigenetics and DNA Methylation (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Joan Atkin collaborates with scholars based in United States, Canada and Switzerland. Joan Atkin's co-authors include Gail E. Herman, Thomas W. Prior, M.B. Nikitovitch-Winer, Bruce E. Maley, Kandamurugu Manickam, Matthew Pastore, Kim L. McBride, Liz Varga, Shivanand R. Patil and James F. Reynolds and has published in prestigious journals such as Endocrinology, Human Molecular Genetics and Genomics.

In The Last Decade

Joan Atkin

19 papers receiving 726 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joan Atkin United States 13 356 342 228 134 83 19 776
Bernard N. Chodirker Canada 15 280 0.8× 293 0.9× 152 0.7× 75 0.6× 31 0.4× 44 752
Perrine Malzac France 13 519 1.5× 574 1.7× 214 0.9× 54 0.4× 81 1.0× 28 881
Hubert Journel France 23 563 1.6× 559 1.6× 191 0.8× 39 0.3× 37 0.4× 57 1.4k
Emmanuelle Lemyre Canada 22 550 1.5× 879 2.6× 276 1.2× 55 0.4× 34 0.4× 52 1.3k
Maria Isabel Melaragno Brazil 20 592 1.7× 893 2.6× 221 1.0× 65 0.5× 42 0.5× 117 1.3k
Judith P. Willner United States 14 631 1.8× 527 1.5× 191 0.8× 159 1.2× 44 0.5× 33 1.2k
Abdul Noor Canada 20 823 2.3× 620 1.8× 118 0.5× 145 1.1× 40 0.5× 42 1.4k
Elisabetta Lapi Italy 18 534 1.5× 477 1.4× 131 0.6× 56 0.4× 49 0.6× 48 957
Maarit Peippo Finland 15 423 1.2× 526 1.5× 100 0.4× 113 0.8× 39 0.5× 24 768
Anne Moncla France 24 1.1k 3.0× 1.3k 3.9× 185 0.8× 343 2.6× 69 0.8× 38 1.9k

Countries citing papers authored by Joan Atkin

Since Specialization
Citations

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

Fields of papers citing papers by Joan Atkin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joan Atkin

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

All Works

19 of 19 papers shown
1.
Pillalamarri, Vamsee, Tammy Kammin, Joan Atkin, et al.. (2016). Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis. Human Molecular Genetics. 25(7). 1255–1270. 27 indexed citations
2.
Hickey, Scott E., Devon Lamb Thrush, Shalini C. Reshmi, et al.. (2013). A case of an atypically large proximal 15q deletion as cause for Prader–Willi syndrome arising from a de novo unbalanced translocation. European Journal of Medical Genetics. 56(9). 510–514. 3 indexed citations
3.
Hickey, Scott E., Sawona Biswas, Devon Lamb Thrush, et al.. (2013). Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion. European Journal of Medical Genetics. 56(9). 521–525. 1 indexed citations
4.
Repnikova, Elena, Caroline Astbury, Shalini C. Reshmi, et al.. (2012). Microarray comparative genomic hybridization and cytogenetic characterization of tissue‐specific mosaicism in three patients. American Journal of Medical Genetics Part A. 158A(8). 1924–1933. 17 indexed citations
5.
Muller, Eric, Swaroop Aradhya, Joan Atkin, et al.. (2011). Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay. American Journal of Medical Genetics Part A. 158A(2). 391–399. 42 indexed citations
6.
McBride, Kim L., Liz Varga, Matthew Pastore, et al.. (2010). Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly. Autism Research. 3(3). 137–141. 185 indexed citations
7.
Cottrell, Catherine E., Thomas W. Prior, Robert E. Pyatt, et al.. (2010). Unexpected detection of dystrophin gene deletions by array comparative genomic hybridization. American Journal of Medical Genetics Part A. 152A(9). 2301–2307. 8 indexed citations
8.
Shell, Richard, Randy R. Miller, Joan Atkin, et al.. (2008). Neonatal Cyanosis Due to a Novel Fetal Hemoglobin: Hb F-Circleville [Gγ63(E7)His→Leu, CAT>CTT]. Hemoglobin. 32(6). 596–600. 16 indexed citations
9.
Hertle, Richard W., et al.. (2005). X-Linked Infantile Periodic Alternating Nystagmus. Ophthalmic Genetics. 26(2). 77–84. 10 indexed citations
10.
Tsao, Chang‐Yong, Gail E. Herman, Daniel R. Boué, et al.. (2003). Leigh Disease With Mitochondrial DNA A8344G Mutation: Case Report and Brief Review. Journal of Child Neurology. 18(1). 62–64. 18 indexed citations
11.
Li, Madeline, Jeremy A. Squire, Cheryl Shuman, et al.. (2001). Imprinting Status of 11p15 Genes in Beckwith–Wiedemann Syndrome Patients with CDKN1C Mutations. Genomics. 74(3). 370–376. 43 indexed citations
12.
13.
Goonewardena, P., et al.. (1992). Prenatally detected fragile X females: Long‐term follow‐up studies show high risk of mental impairment. American Journal of Medical Genetics. 43(1-2). 96–102. 6 indexed citations
14.
Ardinger, Holly H, Joan Atkin, R. Dwain Blackston, et al.. (1988). Verification of the fetal valproate syndrome phenotype. American Journal of Medical Genetics. 29(1). 171–185. 217 indexed citations
15.
Wilson, William G., et al.. (1988). Cytogenetic Studies in Couples With Recurrent Pregnancy Loss. Southern Medical Journal. 81(12). 1521–1524. 2 indexed citations
16.
Nikitovitch-Winer, M.B., Joan Atkin, & Bruce E. Maley. (1987). Colocalization of Prolactin and Growth Hormone within Specific Adenohypophyseal Cells in Male, Female, and Lactating Female Rats. Endocrinology. 121(2). 625–630. 85 indexed citations
17.
Atkin, Joan, et al.. (1985). A new X‐linked mental retardation syndrome. American Journal of Medical Genetics. 21(4). 697–705. 42 indexed citations
18.
Atkin, Joan & Shivanand R. Patil. (1984). Apparently new oculo‐cerebro‐acral syndrome. American Journal of Medical Genetics. 19(3). 585–587. 13 indexed citations
19.
Atkin, Joan, Shivanand R. Patil, & John M. Opitz. (1983). Duplication of the distal segment of 14q. American Journal of Medical Genetics. 16(3). 357–366. 22 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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