Julie C. Sapp

5.1k total citations · 1 hit paper
50 papers, 1.7k citations indexed

About

Julie C. Sapp is a scholar working on Genetics, Surgery and Rheumatology. According to data from OpenAlex, Julie C. Sapp has authored 50 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 20 papers in Surgery and 14 papers in Rheumatology. Recurrent topics in Julie C. Sapp's work include Vascular Malformations and Hemangiomas (20 papers), Soft tissue tumor case studies (10 papers) and Genetic and Kidney Cyst Diseases (9 papers). Julie C. Sapp is often cited by papers focused on Vascular Malformations and Hemangiomas (20 papers), Soft tissue tumor case studies (10 papers) and Genetic and Kidney Cyst Diseases (9 papers). Julie C. Sapp collaborates with scholars based in United States, Canada and Netherlands. Julie C. Sapp's co-authors include Leslie G. Biesecker, Kim M. Keppler‐Noreuil, Jennifer J. Johnston, Marjorie J. Lindhurst, William B. Dobyns, Jonathan J. Rios, Victoria Parker, Robert K. Semple, Marybeth Ezaki and Ahmad I. Alomari and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Julie C. Sapp

48 papers receiving 1.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

PIK3CA‐related overgrowth spectrum (PROS): Diagnostic and testing eligibility criteria, differential diagnosis, and evaluation

2014 326 citations Kim M. Keppler‐Noreuil, Marjorie J. Lindhurst et al. American Journal of Medical Genetics Part A profile →

Peers

Countries citing papers authored by Julie C. Sapp

Since Specialization

Citations

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

Fields of papers citing papers by Julie C. Sapp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julie C. Sapp

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Quantification of Proteus syndrome-associated lung disease 2024 ·Orphanet Journal of Rare Diseases ·(unknown), (unknown), (unknown), Marcus Y. Chen, Julie C. Sapp, Bernadette R. Gochuico, Leslie G. Biesecker	0
2	Case report: five-year experience of AKT inhibition with miransertib (MK-7075) in an individual with Proteus syndrome 2021 ·Molecular Case Studies ·(unknown), Julie C. Sapp, (unknown), (unknown), Leslie G. Biesecker	15
3	Allelic heterogeneity of Proteus syndrome 2020 ·Molecular Case Studies ·(unknown), Marjorie J. Lindhurst, Hannah Kondolf, (unknown), Kim M. Keppler‐Noreuil, Julie C. Sapp, Leslie G. Biesecker	7
4	Orofacial overgrowth with peripheral nerve enlargement and perineuriomatous pseudo-onion bulb proliferations is part of the PIK3CA-related overgrowth spectrum 2020 ·SHILAP Revista de lepidopterología ·Ioannis G. Koutlas, (unknown), (unknown), Ana Sueli Rodrigues Cavalcante, Mohammed Al Kindi, (unknown), Julie C. Sapp, Hannah Kondolf, Marjorie J. Lindhurst, (unknown), Jennifer J. Johnston, (unknown), (unknown), Arupa Ganguly, Leslie G. Biesecker	6
5	Thrombosis risk factors in PIK3CA‐related overgrowth spectrum and Proteus syndrome 2019 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Kim M. Keppler‐Noreuil, Jay N. Lozier, Neal L. Oden, (unknown), (unknown), Julie C. Sapp, Leslie G. Biesecker	24
6	A dyadic genotype–phenotype approach to diagnostic criteria for Proteus syndrome 2019 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Julie C. Sapp, (unknown), (unknown), Kim M. Keppler‐Noreuil, Leslie G. Biesecker	24
7	NAA10 polyadenylation signal variants cause syndromic microphthalmia 2019 ·Journal of Medical Genetics ·Jennifer J. Johnston, Kathleen A. Williamson, (unknown), Julie C. Sapp, Morad Ansari, Heather Chapman, D.N. Cooper, Tabib Dabir, (unknown), Richard Holt, Nicola Ragge, Alejandro A. Schäffer, Shurjo K. Sen, Anne Slavotinek, David Fitzpatrick, Thomas Gläser, Fiona Stewart, Graeme C. Black, Leslie G. Biesecker	22
8	Characterization of the hepatosplenic and portal venous findings in patients with Proteus syndrome 2018 ·American Journal of Medical Genetics Part A ·Varun Takyar, (unknown), Alexander Ling, Rachna Patel, Julie C. Sapp, Sun A. Kim, Sungyoung Auh, Leslie G. Biesecker, Kim M. Keppler‐Noreuil, Theo Heller	3
9	Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome 2018 ·The American Journal of Human Genetics ·(unknown), Hanne Jensen, Jennifer J. Johnston, Emilio Di Maria, Katja Kloth, (unknown), Julie C. Sapp, Thomas N. Darling, Laryssa A. Huryn, Lisbeth Tranebjærg, Élisa Cinotti, Christian Kubisch, Eyvind Rødahl, Ove Bruland, Leslie G. Biesecker, Gunnar Houge, Cecilie Bredrup	18
10	Characterization of thrombosis in patients with Proteus syndrome 2017 ·American Journal of Medical Genetics Part A ·Kim M. Keppler‐Noreuil, Jay N. Lozier, Julie C. Sapp, Leslie G. Biesecker	18
11	Somatic AKT1 mutations cause meningiomas colocalizing with a characteristic pattern of cranial hyperostosis 2016 ·American Journal of Medical Genetics Part A ·Kim M. Keppler‐Noreuil, Eva H. Baker, Julie C. Sapp, Marjorie J. Lindhurst, Leslie G. Biesecker	19
12	Characterization of Courtesy Stigma Perceived by Parents of Overweight Children with Bardet-Biedl Syndrome 2015 ·PLoS ONE ·(unknown), (unknown), (unknown), Leslie G. Biesecker, Barbara B. Biesecker, Julie C. Sapp	37
13	Myocardial fat overgrowth in Proteus syndrome 2014 ·American Journal of Medical Genetics Part A ·Hwaida Hannoush, Vandana Sachdev, Alessandra Brofferio, Andrew E. Arai, Gina LaRocca, Julie C. Sapp, Stanislav Sidenko, (unknown), Leslie G. Biesecker, Kim M. Keppler‐Noreuil	8
14	Expansion of the TARP syndrome phenotype associated with de novo mutations and mosaicism 2013 ·American Journal of Medical Genetics Part A ·Jennifer J. Johnston, Julie C. Sapp, Cynthia J. Curry, Margaret A. Horton, Eyby Leon, Kristina Cusmano‐Ozog, William B. Dobyns, Louanne Hudgins, Elaine H. Zackai, Leslie G. Biesecker	30
15	Research participants’ attitudes towards the confidentiality of genomic sequence information 2013 ·European Journal of Human Genetics ·Leila Jamal, Julie C. Sapp, Katie L. Lewis, Tatiane Yanes, Flavia M. Facio, Leslie G. Biesecker, Barbara B. Biesecker	37
16	The Phenotype of a Germline Mutation in PIGA: The Gene Somatically Mutated in Paroxysmal Nocturnal Hemoglobinuria 2012 ·The American Journal of Human Genetics ·Jennifer J. Johnston, Andrea Gropman, Julie C. Sapp, Jamie K. Teer, (unknown), (unknown), Xuan Yuan, Zhaohui Ye, Linzhao Cheng, Robert A. Brodsky, Leslie G. Biesecker	110
17	Brain tissue- and region-specific abnormalities on volumetric MRI scans in 21 patients with Bardet-Biedl syndrome (BBS) 2011 ·BMC Medical Genetics ·Kim M. Keppler‐Noreuil, (unknown), Julie C. Sapp, (unknown), Jennifer J. Johnston, Peg Nopoulos, Leslie G. Biesecker	33
18	Recurrence risks for Bardet-Biedl syndrome: Implications of locus heterogeneity 2010 ·Genetics in Medicine ·Julie C. Sapp, Darryl Nishimura, Jennifer J. Johnston, Edwin M. Stone, Elise Héon, Val C. Sheffield, Leslie G. Biesecker	11
19	Ambivalence toward undergoing invasive prenatal testing: an exploration of its origins 2009 ·Prenatal Diagnosis ·Julie C. Sapp, Sara Chandros Hull, (unknown), (unknown), Erica J. Sutton, Theresa M. Marteau, Barbara B. Biesecker	23
20	Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patients 2007 ·American Journal of Medical Genetics Part A ·Julie C. Sapp, Joyce Turner, Jiddeke M. van de Kamp, Fleur S van Dijk, R. Brian Lowry, Leslie G. Biesecker	141

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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