Natalie Deuitch

3.0k total citations
26 papers, 325 citations indexed

About

Natalie Deuitch is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Natalie Deuitch has authored 26 papers receiving a total of 325 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 8 papers in Hematology. Recurrent topics in Natalie Deuitch's work include Acute Myeloid Leukemia Research (7 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (4 papers) and Peptidase Inhibition and Analysis (4 papers). Natalie Deuitch is often cited by papers focused on Acute Myeloid Leukemia Research (7 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (4 papers) and Peptidase Inhibition and Analysis (4 papers). Natalie Deuitch collaborates with scholars based in United States, Canada and China. Natalie Deuitch's co-authors include Ivona Aksentijevich, Cornelia Cudrici, Mark Peifer, Mira I. Pronobis, Qing Zhou, Meiping Lu, Danton Char, Amanda K. Ombrello, Sandra Soo‐Jin Lee and Hong Jiang and has published in prestigious journals such as Blood, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Natalie Deuitch

20 papers receiving 324 citations

Peers

Countries citing papers authored by Natalie Deuitch

Since Specialization

Citations

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

Fields of papers citing papers by Natalie Deuitch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natalie Deuitch

This figure shows the co-authorship network connecting the top 25 collaborators of Natalie Deuitch. A scholar is included among the top collaborators of Natalie Deuitch 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 Natalie Deuitch. Natalie Deuitch 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	Hematologic malignancies in pediatric patients with RUNX1-Familial Platelet Disorder with Associated Myeloid Malignancy 2026 ·Blood Advances ·(unknown), Natalie Deuitch, Erica Bresciani, (unknown), (unknown), (unknown), (unknown), Lisa J. McReynolds, (unknown), (unknown), (unknown)	0
2	Correspondence on “ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)” by Lee et al 2026 ·Genetics in Medicine ·Natalie Deuitch, (unknown), David J. Young, Dan Wu, (unknown)	0
3	Pregnancy and delivery outcomes in individuals with RUNX1‐Familial Platelet Disorder 2025 ·British Journal of Haematology ·Natalie Deuitch, (unknown), (unknown), Erica Bresciani, K. L. Craft, Joie Davis, (unknown), David J. Young, Paul Liu	1
4	Proteasome-Associated Syndromes: Updates on Genetics, Clinical Manifestations, Pathogenesis, and Treatment 2024 ·Journal of Clinical Immunology ·Jiahui Zhang, Panfeng Tao, Natalie Deuitch, Xiaomin Yu, (unknown), Qing Zhou	2
5	Minority Patients in the NIH RUNX1-FPDMM Natural History Study Present Mostly with Large Deletions Affecting RUNX1 2024 ·Blood ·(unknown), Natalie Deuitch, Erica Bresciani, (unknown), (unknown), (unknown), David J. Young, Paul Liu	0
6	Donor-Derived Malignancy and Transplantation Morbidity: Risks of Patient and Donor Genetics in Allogeneic Hematopoietic Stem Cell Transplantation 2023 ·Transplantation and Cellular Therapy ·(unknown), Kirsten M. Williams, Nancy Gillis, Kelly L. Bolton, Frédérik Damm, Natalie Deuitch, Nosha Farhadfar, Usama Gergis, Sioḃán Keel, Fotios V. Michelis, Sandhya R. Panch, Christopher C. Porter, Lara E. Sucheston‐Campbell, Roni Tamari, Heather E. Stefanski, Lucy A. Godley, Catherine Lai	10
7	Genomic landscape of patients with germline RUNX1 variants and familial platelet disorder with myeloid malignancy 2023 ·Blood Advances ·Kai Yu, Natalie Deuitch, (unknown), Lea Cunningham, Joie Davis, Erica Bresciani, (unknown), (unknown), Alice Young, Frank X. Donovan, Raman Sood, (unknown), (unknown), Settara C. Chandrasekharappa, (unknown), Paul Liu	9
8	The Perceived Influence of Neurofibromatosis Type 1(NF1) on the Parents’ Relationship 2023 ·Children ·Lori Wiener, (unknown), (unknown), (unknown), Natalie Deuitch, Brigitte C. Widemann	0
9	A framework to identify ethical concerns with ML-guided care workflows: a case study of mortality prediction to guide advance care planning 2023 ·Journal of the American Medical Informatics Association ·(unknown), Natalie Deuitch, Nigam H. Shah, Chris Feudtner, Danton Char	8
10	TNF-Blockade for Primary Stroke Prevention in Adenosine Deaminase 2 Deficiency 2023 ·Neurology Neuroimmunology & Neuroinflammation ·Ariane Soldatos, Camilo Toro, Patrycja Hoffmann, Tina Romeo, Natalie Deuitch, Alessandra Brofferio, Ivona Aksentijevich, Daniel L. Kastner, Amanda K. Ombrello	5
11	Parental Attitudes Toward Clinical Genomic Sequencing in Children With Critical Cardiac Disease 2021 ·Pediatric Critical Care Medicine ·(unknown), Natalie Deuitch, Sandra Soo‐Jin Lee, (unknown), Danton Char	7
12	“Doctors can read about it, they can know about it, but they've never lived with it”: How parents use social media throughout the diagnostic odyssey 2021 ·Journal of Genetic Counseling ·Natalie Deuitch, (unknown), Meghan C. Halley, Jennifer L. Young, Chloe M. Reuter, Jennefer N. Kohler, Jonathan A. Bernstein, Matthew T. Wheeler, (unknown), Kelly E. Ormond, Holly K. Tabor	13
13	Early-onset breast cancer in a woman with a germline mobile element insertion resulting in BRCA2 disruption: a case report 2020 ·Human Genome Variation ·Natalie Deuitch, (unknown), Eliza Courtney, (unknown), Rebecca Dent, Veronique Kiak Mien Tan, (unknown), Rebecca I. Torene, Windy Berkofsky‐Fessler, Joanne Ngeow	3
14	Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance 2020 ·Journal of Clinical Immunology ·Oskar Schnappauf, Qing Zhou, Natalia Sampaio Moura, Amanda K. Ombrello, Drew G. Michael, Natalie Deuitch, Karyl S. Barron, Deborah L. Stone, Patrycja Hoffmann, Michael S. Hershfield, Carolyn Applegate, Hans T. Björnsson, David B. Beck, P. Dane Witmer, Nara Sobreira, Elizabeth Wohler, John A. Chiorini, Clifton L. Dalgard, Daniel L. Kastner, Ivona Aksentijevich	27
15	Attitudes Toward Hypothetical Uses of Gene-Editing Technologies in Parents of People with Autosomal Aneuploidies 2019 ·The CRISPR Journal ·(unknown), Natalie Deuitch, Marsha Michie, Megan Allyse, Kirsten A. Riggan, Kelly E. Ormond	17
16	Haploinsufficiency of A20 (HA20): updates on the genetics, phenotype, pathogenesis and treatment 2019 ·World Journal of Pediatrics ·(unknown), (unknown), Qing Zhou, Natalie Deuitch, Meiping Lu	53
17	Translating genomic testing results for pediatric critical care: Opportunities for genetic counselors 2019 ·Journal of Genetic Counseling ·Natalie Deuitch, Sandra Soo‐Jin Lee, Danton Char	14
18	Deficiency of Adenosine Deaminase 2 in Adult Siblings: Many Years of a Misdiagnosed Disease With Severe Consequences 2018 ·Frontiers in Immunology ·Jason Springer, Selina Gierer, Hong Jiang, David E. Kleiner, Natalie Deuitch, Amanda K. Ombrello, Peter C. Grayson, Ivona Aksentijevich	34
19	The Miraprep: A Protocol that Uses a Miniprep Kit and Provides Maxiprep Yields 2016 ·PLoS ONE ·Mira I. Pronobis, Natalie Deuitch, Mark Peifer	38
20	Reconstituting regulation of the canonical Wnt pathway by engineering a minimal β-catenin destruction machine 2016 ·Molecular Biology of the Cell ·Mira I. Pronobis, Natalie Deuitch, (unknown), Yuko Mimori‐Kiyosue, Mark Peifer	21

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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