Dana Neitzel

589 total citations
14 papers, 111 citations indexed

About

Dana Neitzel is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Dana Neitzel has authored 14 papers receiving a total of 111 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 8 papers in Genetics and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Dana Neitzel's work include Prenatal Screening and Diagnostics (9 papers), Cystic Fibrosis Research Advances (5 papers) and Genetic Syndromes and Imprinting (4 papers). Dana Neitzel is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Cystic Fibrosis Research Advances (5 papers) and Genetic Syndromes and Imprinting (4 papers). Dana Neitzel collaborates with scholars based in United States. Dana Neitzel's co-authors include Valerie Greger, Nicole Faulkner, Tuan Dinh, Stephanie Hallam, Cynthia L. Perreault-Micale, Caleb J. Kennedy, Mark A. Umbarger, Sara L. Bristow, Gregory J. Porreca and Niru Chennagiri and has published in prestigious journals such as Fertility and Sterility, Human Mutation and Genetics in Medicine.

In The Last Decade

Dana Neitzel

12 papers receiving 104 citations

Peers

Dana Neitzel
Lauren Westerfield United States
Telma Barbosa Portugal
Sandra Cindrić Germany
Melissa Crenshaw United States
Françoise Girard‐Lemaire France
Séverine Audebert‐Bellanger France
Olivier Patat France
Céline Pebrel‐Richard France
Lamisse Mansour‐Hendili France
Helen Dolling United Kingdom
Lauren Westerfield United States
Dana Neitzel
Citations per year, relative to Dana Neitzel Dana Neitzel (= 1×) peers Lauren Westerfield

Countries citing papers authored by Dana Neitzel

Since Specialization
Citations

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

Fields of papers citing papers by Dana Neitzel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dana Neitzel

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

All Works

14 of 14 papers shown
1.
Neitzel, Dana, et al.. (2024). Derivative and non-derivative aneuploidy rates in PGT tested blastocysts from carriers of structural rearrangements. Reproductive BioMedicine Online. 50(3). 104407–104407.
2.
Neitzel, Dana, et al.. (2022). eP472: Deriving risk estimates for balanced rearrangement carriers utilizing PGT-SR data. Genetics in Medicine. 24(3). S299–S300. 1 indexed citations
3.
Neitzel, Dana, et al.. (2021). CLINICAL UTILITY OF HUMAN REVIEW: EXPERIENCE WITH PREVIOUSLY UNKNOWN REARRANGEMENT CARRIERS USING FAST-SEQS, A NEXT-GENERATION SEQUENCING PGT ASSAY. Fertility and Sterility. 116(3). e398–e398. 1 indexed citations
4.
Neitzel, Dana, et al.. (2021). Experience analysing over 190,000 embryo trophectoderm biopsies using a novel FAST-SeqS preimplantation genetic testing assay. Reproductive BioMedicine Online. 44(2). 228–238. 9 indexed citations
5.
Nykamp, Keith, Rebecca Truty, Sara L. Bristow, et al.. (2021). Elucidating clinical phenotypic variability associated with the polyT tract and TG repeats in CFTR. Human Mutation. 42(9). 1165–1172. 13 indexed citations
6.
Neitzel, Dana, et al.. (2019). Carrier screening: should evaluating more genes be the standard of care?. Fertility and Sterility. 111(4). e33–e34. 2 indexed citations
7.
8.
Umbarger, Mark A., et al.. (2017). Targeted next generation sequencing-based pgs can enable detection of uniparental isodisomy, familial relationships, and polyploidy. Fertility and Sterility. 108(3). e270–e270. 1 indexed citations
9.
Neitzel, Dana, et al.. (2017). Re-biopsied pgs embryos yield actionable results. Fertility and Sterility. 108(3). e290–e290. 3 indexed citations
10.
Neitzel, Dana, et al.. (2017). Aneuploidy rates in day 5 vs day 6 biopsies. Fertility and Sterility. 108(3). e283–e284.
11.
Greger, Valerie, et al.. (2016). Carrier screening by next‐generation sequencing: health benefits and cost effectiveness. Molecular Genetics & Genomic Medicine. 4(3). 292–302. 38 indexed citations
12.
Hallam, Stephanie, Heather H. Nelson, Valerie Greger, et al.. (2014). Validation for Clinical Use of, and Initial Clinical Experience with, a Novel Approach to Population-Based Carrier Screening using High-Throughput, Next-Generation DNA Sequencing. Journal of Molecular Diagnostics. 16(2). 180–189. 31 indexed citations
13.
Perreault-Micale, Cynthia L., Caleb J. Kennedy, Dana Neitzel, et al.. (2014). Truncating Variants in the Majority of the Cytoplasmic Domain of PCDH15 Are Unlikely to Cause Usher Syndrome 1F. Journal of Molecular Diagnostics. 16(6). 673–678. 10 indexed citations
14.

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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