Julie Kaplan

777 total citations
16 papers, 213 citations indexed

About

Julie Kaplan is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Julie Kaplan has authored 16 papers receiving a total of 213 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Surgery. Recurrent topics in Julie Kaplan's work include Genetic Syndromes and Imprinting (2 papers), BRCA gene mutations in cancer (2 papers) and Protein Tyrosine Phosphatases (2 papers). Julie Kaplan is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), BRCA gene mutations in cancer (2 papers) and Protein Tyrosine Phosphatases (2 papers). Julie Kaplan collaborates with scholars based in United States, Germany and United Kingdom. Julie Kaplan's co-authors include Louanne Hudgins, Andrea Kwan, Jonathan A. Bernstein, Marie‐Louise Briard, J Rigó, Alain Verloès, Constantinos Pángalos, D Soyeur, Geranda Notten and Marie Le Merrer and has published in prestigious journals such as PEDIATRICS, The Gerontologist and Journal of Molecular Medicine.

In The Last Decade

Julie Kaplan

14 papers receiving 213 citations

Peers

Julie Kaplan

GENET

PPCH

PRM

Silvia Vannelli Italy

Chiara Castronovo Italy

Annamaria Perri Italy

Virginie Kinet Belgium

Robert Röhle Germany

Lisa J. Brothman United States

A O'Rourke United Kingdom

A. de la Chapelle France

Cassandra McDonald Canada

Nadja Kokalj Vokač Slovenia

Silvia Vannelli Italy

Julie Kaplan

86 ×0.8

71 ×0.7

GENET

39 ×1.3

28 ×1.2

PPCH

8 ×0.4

PRM

Citations per year, relative to Julie Kaplan Julie Kaplan (= 1×) peers Silvia Vannelli

Countries citing papers authored by Julie Kaplan

Since Specialization

Citations

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

Fields of papers citing papers by Julie Kaplan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julie Kaplan

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

Hendon, Laura G., et al.. (2021). Asynchronous telemedicine for clinical genetics consultations in the NICU: a single center’s solution. Journal of Perinatology. 42(2). 262–268. 3 indexed citations

Gripp, Karen W., Sarah Smithson, Ingrid Scurr, et al.. (2021). Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3—a subgroup of K+ channelopathies. European Journal of Human Genetics. 29(9). 1384–1395. 25 indexed citations

Averdunk, Luisa, Heinrich Sticht, Harald Surowy, et al.. (2021). The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype. Journal of Molecular Medicine. 99(12). 1755–1768. 4 indexed citations

Notten, Geranda & Julie Kaplan. (2021). Material Deprivation: Measuring Poverty by Counting Necessities Households Cannot Afford. Canadian Public Policy. 47(1). 1–17. 7 indexed citations

Notten, Geranda & Julie Kaplan. (2021). An Empirical Validation Method for Narrowing the Range of Poverty Thresholds. Social Indicators Research. 161(1). 251–271. 2 indexed citations

Cohen, Jennifer L., Kelly A. Duffy, Jennifer Richards‐Yutz, et al.. (2019). Diagnosis and management of the phenotypic spectrum of twins with Beckwith‐Wiedemann syndrome. American Journal of Medical Genetics Part A. 179(7). 1139–1147. 18 indexed citations

Kaplan, Julie, et al.. (2017). Using Telemedicine in Mississippi to Improve Patient Access to Genetic Services. Journal of Genetic Counseling. 27(2). 320–322. 15 indexed citations

Asoğlu, Mehmet Reşit, et al.. (2017). The importance of prenatal 3‐dimensional sonography in a case of a segmental overgrowth syndrome with unclear chromosomal microarray results. Journal of Clinical Ultrasound. 46(5). 351–354. 2 indexed citations

Lin, Angela E., Caroline Michot, Valérie Cormier‐Daire, et al.. (2016). Gain‐of‐function mutations in SMAD4 cause a distinctive repertoire of cardiovascular phenotypes in patients with Myhre syndrome. American Journal of Medical Genetics Part A. 170(10). 2617–2631. 45 indexed citations

10.

Kaplan, Julie, et al.. (2014). IMAGe syndrome in the era of genetic testing: clues to diagnosis. Case Reports in Perinatal Medicine. 4(1). 65–68.

11.

Kaplan, Julie, Jonathan A. Bernstein, Andrea Kwan, & Louanne Hudgins. (2010). Clues to an early diagnosis of Kallmann syndrome. American Journal of Medical Genetics Part A. 152A(11). 2796–2801. 34 indexed citations

12.

Kaplan, Julie & Louanne Hudgins. (2008). Neonatal Presentations of CHARGE Syndrome and VATER/VACTERL Association. NeoReviews. 9(7). e299–e304. 4 indexed citations

13.

Shieh, Joseph T.C., John A. Martignetti, Maria Celeste M. Ramirez, et al.. (2006). Systemic Hyalinosis: A Distinctive Early Childhood–Onset Disorder Characterized by Mutations in the Anthrax Toxin Receptor 2 Gene (ANTRX2). PEDIATRICS. 118(5). e1485–e1492. 20 indexed citations

14.

Verloès, Alain, Marie Le Merrer, D Soyeur, et al.. (1988). CFC syndrome: a syndrome distinct from Noonan syndrome.. PubMed. 31(4). 230–4. 33 indexed citations

15.

Merrer, M. Le, et al.. (1984). [Malformation uropathies and multiple malformation syndromes].. PubMed. 32(2). 83–90. 1 indexed citations

16.

Kaplan, Julie. (1970). Social Planning -- A Continuing Challenge. The Gerontologist. 10(3 Part 1). 189–189.

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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