Julie Neidich

2.6k total citations
42 papers, 698 citations indexed

About

Julie Neidich is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Julie Neidich has authored 42 papers receiving a total of 698 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 10 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Julie Neidich's work include Cleft Lip and Palate Research (7 papers), Metabolism and Genetic Disorders (6 papers) and Craniofacial Disorders and Treatments (5 papers). Julie Neidich is often cited by papers focused on Cleft Lip and Palate Research (7 papers), Metabolism and Genetic Disorders (6 papers) and Craniofacial Disorders and Treatments (5 papers). Julie Neidich collaborates with scholars based in United States, Italy and France. Julie Neidich's co-authors include Jennifer M. Puck, Denise Salazar, J A Kant, D. Hicks, Virginia A. LiVolsi, Roger J. Packer, Fred Lorey, Robert L. Nussbaum, B S Emanuel and Orrin Devinsky and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and The American Journal of Human Genetics.

In The Last Decade

Julie Neidich

40 papers receiving 679 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julie Neidich United States 17 270 231 148 138 97 42 698
Siddharth Banka United Kingdom 18 339 1.3× 480 2.1× 69 0.5× 85 0.6× 104 1.1× 55 991
Pilar Magoulas United States 15 383 1.4× 290 1.3× 132 0.9× 147 1.1× 73 0.8× 24 727
Matias Wagner Germany 16 447 1.7× 225 1.0× 73 0.5× 133 1.0× 37 0.4× 83 792
Heather J. Church United Kingdom 19 226 0.8× 127 0.5× 125 0.8× 42 0.3× 44 0.5× 70 1.1k
J. W. E. Oorthuys Netherlands 12 211 0.8× 345 1.5× 87 0.6× 63 0.5× 66 0.7× 25 558
Peggy Modaff United States 15 229 0.8× 297 1.3× 108 0.7× 34 0.2× 86 0.9× 35 625
Jodi D. Hoffman United States 18 215 0.8× 365 1.6× 119 0.8× 32 0.2× 52 0.5× 33 654
Eiichi Kinoshita Japan 16 411 1.5× 303 1.3× 67 0.5× 28 0.2× 87 0.9× 51 775
David O. Sillence Australia 12 335 1.2× 230 1.0× 54 0.4× 32 0.2× 77 0.8× 16 782
Sumito Dateki Japan 14 286 1.1× 293 1.3× 50 0.3× 56 0.4× 134 1.4× 40 592

Countries citing papers authored by Julie Neidich

Since Specialization
Citations

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

Fields of papers citing papers by Julie Neidich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julie Neidich

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

All Works

20 of 20 papers shown
1.
Bowling, Kevin M., Alexa Dickson, Molly C. Schroeder, et al.. (2024). Modified Rules for Classification of Variants Associated With Disorders of Somatic Mosaicism. Clinical Genetics. 107(3). 261–270. 3 indexed citations
2.
Ghasemi, Reza, Kevin M. Bowling, Kilannin Krysiak, et al.. (2024). Comprehensive Analysis of TEK Variants in Patients With Vascular Malformations. Clinical Genetics. 107(4). 458–462.
3.
King, Katherine A., et al.. (2023). High‐depth next‐generation sequencing panel testing in the evaluation of arteriovenous malformations. American Journal of Medical Genetics Part A. 191(6). 1518–1524. 2 indexed citations
4.
Schroeder, Molly C., et al.. (2023). Co-existence of 2 clinically significant variants causing disorders of somatic mosaicism. SHILAP Revista de lepidopterología. 1(1). 100807–100807. 4 indexed citations
5.
Hecker, Julian, et al.. (2023). Fallacies and Pitfalls in Genome-Wide Association Studies. 4(2). 1 indexed citations
6.
Mojarad, Bahareh A., Sarah L. Stein, Amy Theos, et al.. (2023). Profiling PIK3CA variants in disorders of somatic mosaicism. SHILAP Revista de lepidopterología. 1(1). 100815–100815. 1 indexed citations
7.
Hou, Ying‐Chen Claire, Julie Neidich, Eric J. Duncavage, David H. Spencer, & Molly C. Schroeder. (2022). Clinical whole‐genome sequencing in cancer diagnosis. Human Mutation. 43(11). 1519–1530. 13 indexed citations
8.
Mansi, Laura, Cristian Villanueva, Fabien Calcagno, et al.. (2017). First description of a double heterozygosity for BRCA1 and BRCA2 pathogenic variants in a French metastatic breast cancer patient: A case report. Oncology Reports. 37(3). 1573–1578. 10 indexed citations
9.
Kammesheidt, Anja, et al.. (2016). Mutation detection in cell free DNA from healthy donors.. Journal of Clinical Oncology. 34(15_suppl). e23054–e23054. 3 indexed citations
10.
Cederbaum, Stephen D., Julie Neidich, Natalie M. Gallant, et al.. (2013). Analysis of cases of 3-methylcrotonyl CoA carboxylase deficiency (3-MCCD) in the California newborn screening program reported in the state database. Molecular Genetics and Metabolism. 110(4). 477–483. 18 indexed citations
11.
Arnold, Georgianne L., Denise Salazar, Julie Neidich, et al.. (2012). Outcome of infants diagnosed with 3-methyl-crotonyl-CoA-carboxylase deficiency by newborn screening. Molecular Genetics and Metabolism. 106(4). 439–441. 18 indexed citations
12.
Gallant, Natalie M., Hao Tang, Lisa Feuchtbaum, et al.. (2012). Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California. Molecular Genetics and Metabolism. 106(1). 55–61. 44 indexed citations
13.
Park, Noh Jin, Morgan Craig, Rajesh Sharma, et al.. (2010). Improving Accuracy of Tay Sachs Carrier Screening of the Non-Jewish Population: Analysis of 34 Carriers and Six Late-Onset Patients With HEXA Enzyme and DNA Sequence Analysis. Pediatric Research. 67(2). 217–220. 15 indexed citations
14.
Lin, Henry J., Julie Neidich, Denise Salazar, et al.. (2009). Asymptomatic Maternal Combined Homocystinuria and Methylmalonic Aciduria (cblC) Detected through Low Carnitine Levels on Newborn Screening. The Journal of Pediatrics. 155(6). 924–927. 27 indexed citations
15.
Crombez, Eric, Stephen D. Cederbaum, Elaine Spector, et al.. (2008). Maternal glutaric acidemia, type I identified by newborn screening. Molecular Genetics and Metabolism. 94(1). 132–134. 30 indexed citations
16.
Neidich, Julie. (2005). Inborn Errors of Development: The Molecular Basis of Clinical Disorders of Morphogenesis.. The American Journal of Human Genetics. 76(2). 368–368. 54 indexed citations
17.
Cormier‐Daire, Valérie, et al.. (2001). ?Baby rattle? pelvis dysplasia. American Journal of Medical Genetics. 100(1). 37–42. 1 indexed citations
18.
Robin, Nathaniel H., Julie Neidich, Lynn Bason, et al.. (1996). Frontonasal malformation and cloacal exstrophy: A previously unreported association. American Journal of Medical Genetics. 61(1). 75–78. 9 indexed citations
19.
Druzin, Maurice L., et al.. (1993). Should all pregnant patients be offered prenatal diagnosis regardless of age?. PubMed. 81(4). 615–8. 24 indexed citations
20.
Neidich, Julie, Elaine H. Zackai, M.M. Aronson, et al.. (1987). Deletion of 2p: A cytogenetic and clinical update. American Journal of Medical Genetics. 27(3). 707–710. 24 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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