Julie Scuffins

561 total citations
10 papers, 348 citations indexed

About

Julie Scuffins is a scholar working on Genetics, Psychiatry and Mental health and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Julie Scuffins has authored 10 papers receiving a total of 348 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Psychiatry and Mental health and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Julie Scuffins's work include Genomics and Rare Diseases (5 papers), Cerebral Palsy and Movement Disorders (4 papers) and Prenatal Screening and Diagnostics (3 papers). Julie Scuffins is often cited by papers focused on Genomics and Rare Diseases (5 papers), Cerebral Palsy and Movement Disorders (4 papers) and Prenatal Screening and Diagnostics (3 papers). Julie Scuffins collaborates with scholars based in United States and Canada. Julie Scuffins's co-authors include Kyle Retterer, Jane Juusola, Bethany Friedman, Kristin G. Monaghan, Gabriele Richard, Rebecca I. Torene, Jeanne Meck, Vladimir G. Gainullin, Kevin J. Arvai and Eden Haverfield and has published in prestigious journals such as JAMA, Neurology and Genetics in Medicine.

In The Last Decade

Julie Scuffins

7 papers receiving 340 citations

Peers

Julie Scuffins

GENET

PPCH

MB

PMH

GENET

Joo Wook Ahn United Kingdom

Maria Paola Recalcati Italy

Frédérique Tihy Canada

Alison Yeung Australia

Ho‐Ming Luk China

Magdalena Bartnik Poland

Lee Zellmer United States

Rachel D. Burnside United States

Janet Marcadier Canada

Mondher Chouchane France

Joo Wook Ahn United Kingdom

Julie Scuffins

424 ×2.0

GENET

159 ×1.3

PPCH

232 ×1.9

MB

16 ×0.4

PMH

34 ×0.9

GENET

Citations per year, relative to Julie Scuffins Julie Scuffins (= 1×) peers Joo Wook Ahn

Countries citing papers authored by Julie Scuffins

Since Specialization

Citations

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

Fields of papers citing papers by Julie Scuffins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julie Scuffins

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

All Works

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10 of 10 papers shown

1.

Moreno-De-Luca, Andrés, Francisca Millan, Houda Zghal Elloumi, et al.. (2021). Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy. JAMA. 325(5). 467–467. 71 indexed citations

2.

Scuffins, Julie, Jennifer Keller‐Ramey, Ganka Douglas, et al.. (2021). Uniparental disomy in a population of 32,067 clinical exome trios. Genetics in Medicine. 23(6). 1101–1107. 38 indexed citations

3.

Moreno-De-Luca, Andrés, Francisca Millan, Houda Zghal Elloumi, et al.. (2021). Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy. Obstetrical & Gynecological Survey. 76(7). 399–401.

4.

Torene, Rebecca I., Kevin Galens, Shuxi Liu, et al.. (2020). Mobile element insertion detection in 89,874 clinical exomes. Genetics in Medicine. 22(5). 974–978. 39 indexed citations

5.

Zou, Fanggeng, et al.. (2019). A Comprehensive and Dynamic Approach for Genetic Testing for Patient with Leukodystrophy Demonstrates a Genetic Etiology in 33% of Cases (P4.6-054). Neurology. 92(15_supplement).

6.

Millan, Francisca, et al.. (2019). Genetic testing of >1300 patients with cerebral palsy reveals an etiology in one-third of cases, underscoring the need for broad genetic testing and a significant recurrence risk for families. (P4.6-028). Neurology. 92(15_supplement). 1 indexed citations

7.

Millan, Francisca, et al.. (2019). Genetic testing of >1300 patients with cerebral palsy reveals an etiology in one-third of cases, underscoring the need for broad genetic testing and a significant recurrence risk for families. (P4.6-028). 92. 1 indexed citations

8.

Monaghan, Kristin G., Kyle Retterer, Julie Scuffins, et al.. (2017). Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal development. Genetics in Medicine. 19(10). 1171–1178. 112 indexed citations

9.

Millan, Francisca, Dianalee McKnight, Julie Scuffins, et al.. (2017). EXOME SEQUENCING OFFERS A COMPREHENSIVE GENETIC EVALUATION AND HIGH DIAGNOSTIC RATE FOR ATAXIA-RELATED DISORDERS (S17.004). Neurology. 88(16_supplement).

10.

Retterer, Kyle, Julie Scuffins, Daniel Schmidt, et al.. (2014). Assessing copy number from exome sequencing and exome array CGH based on CNV spectrum in a large clinical cohort. Genetics in Medicine. 17(8). 623–629. 86 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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