Matthew A. Deardorff

11.1k total citations
109 papers, 3.6k citations indexed

About

Matthew A. Deardorff is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Matthew A. Deardorff has authored 109 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 48 papers in Genetics and 19 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Matthew A. Deardorff's work include Genomics and Chromatin Dynamics (24 papers), Genomic variations and chromosomal abnormalities (16 papers) and Genetic Syndromes and Imprinting (15 papers). Matthew A. Deardorff is often cited by papers focused on Genomics and Chromatin Dynamics (24 papers), Genomic variations and chromosomal abnormalities (16 papers) and Genetic Syndromes and Imprinting (15 papers). Matthew A. Deardorff collaborates with scholars based in United States, Canada and Italy. Matthew A. Deardorff's co-authors include Peter S. Klein, Ian D. Krantz, Change Tan, Elaine H. Zackai, Nancy B. Spinner, Laura K. Conlin, Håkon Håkonarson, Maninder Kaur, Dinah Clark and Brian Thiel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and The EMBO Journal.

In The Last Decade

Matthew A. Deardorff

102 papers receiving 3.5k citations

Peers

Countries citing papers authored by Matthew A. Deardorff

Since Specialization

Citations

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

Fields of papers citing papers by Matthew A. Deardorff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew A. Deardorff. 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 Matthew A. Deardorff. The network helps show where Matthew A. Deardorff may publish in the future.

Co-authorship network of co-authors of Matthew A. Deardorff

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew A. Deardorff. A scholar is included among the top collaborators of Matthew A. Deardorff 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 Matthew A. Deardorff. Matthew A. Deardorff 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	16q24.3 Microdeletions Disrupting Upstream Non-Coding Region of ANKRD11 Cause KBG Syndrome 2025 ·Genes ·Aiko Iwata‐Otsubo, (unknown), Jorune Balciuniene, (unknown), (unknown), (unknown), Cara Skraban, Christopher Gray, Elaine H. Zackai, Holly Dubbs, Matthew A. Deardorff, Laura K. Conlin, Kosuke Izumi	1
2	Autonomous drone behavior via MCDM of UFOMap layers 2024 ·(unknown), (unknown), (unknown), (unknown), Matthew A. Deardorff, Derek T. Anderson, Robert H. Luke	0
3	Improving Real-Time Aerial 3D Reconstruction: Towards Fusion of a Hand-Crafted SfM Algorithm with a Data-Driven Deep Neural Network 2023 ·(unknown), (unknown), Derek T. Anderson, James M. Keller, (unknown), Matthew A. Deardorff, Robert Luke	0
4	The chromatin remodeler ISWI acts during Drosophila development to regulate adult sleep 2021 ·Science Advances ·Naihua N. Gong, (unknown), (unknown), Emilia H. Moscato, Milán Szuperák, Qin Wang, Matthew Jensen, Santhosh Girirajan, Tiong Yang Tan, Matthew A. Deardorff, Dong Li, Yuanquan Song, Matthew S. Kayser	9
5	A novel pathogenic missense ADAMTS17 variant that impairs secretion causes Weill-Marchesani Syndrome with variably dysmorphic hand features 2020 ·Scientific Reports ·(unknown), Jane S. Green, Somayyeh Fahiminiya, Jacek Majewski, Bridget A. Fernandez, Matthew A. Deardorff, (unknown), (unknown), Dirk Hubmacher, Suneel Apte, Kym M. Boycott, Dennis E. Bulman, David A. Dyment, (unknown), Michael Brudno, Michael O. Woods	14
6	Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach 2019 ·European Journal of Human Genetics ·Chao Wu, Batsal Devkota, Perry Evans, Xiaonan Zhao, Samuel W. Baker, (unknown), Kajia Cao, Michael Gonzalez, Pushkala Jayaraman, Laura K. Conlin, Bryan L. Krock, Matthew A. Deardorff, Nancy B. Spinner, Ian D. Krantz, Avni Santani, Ahmad Abou Tayoun, Mahdi Sarmady	10
7	TRPV6 Variants Interfere with Maternal-Fetal Calcium Transport through the Placenta and Cause Transient Neonatal Hyperparathyroidism 2018 ·The American Journal of Human Genetics ·Yoshiro Suzuki, David Chitayat, Hirotake Sawada, Matthew A. Deardorff, Heather M. McLaughlin, Amber Begtrup, (unknown), Jennifer Harrington, Karen Chong, Maian Roifman, Katheryn Grand, Makoto Tominaga, Fumio Takada, (unknown), (unknown), H. Mutoh, (unknown), Gen Nishimura	54
8	The utility of alpha‐fetoprotein screening in Beckwith–Wiedemann syndrome 2017 ·American Journal of Medical Genetics Part A ·Kelly A. Duffy, Matthew A. Deardorff, Jennifer M. Kalish	13
9	Fetal akinesia deformation sequence due to a congenital disorder of glycosylation 2015 ·American Journal of Medical Genetics Part A ·Rebecca Ganetzky, Kosuke Izumi, Andrew C. Edmondson, Colleen Muraresku, Elaine H. Zackai, Matthew A. Deardorff, Jaya Ganesh	11
10	Mutations in the ABCC6 Gene as a Cause of Generalized Arterial Calcification of Infancy: Genotypic Overlap with Pseudoxanthoma Elasticum 2013 ·Journal of Investigative Dermatology ·Qiaoli Li, Jill L. Brodsky, Laura K. Conlin, Bruce Pawel, Andrew C. Glatz, Rachel I. Gafni, Leon J. Schurgers, Jouni Uitto, Håkon Håkonarson, Matthew A. Deardorff, Michael A. Levine	59
11	Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low‐Level Uniparental Disomy 2013 ·American Journal of Medical Genetics Part A ·Jennifer M. Kalish, Laura K. Conlin, Sogol Mostoufi‐Moab, Alisha Wilkens, Surabhi Mulchandani, Kristin Zelley, (unknown), Tricia Bhatti, Pierre Russo, Peter Mattei, William G. Mackenzie, Virginia A. LiVolsi, Kim E. Nichols, Jaclyn A. Biegel, Nancy B. Spinner, Matthew A. Deardorff	15
12	Whole-Exome Sequencing Identifies Mutated C12orf57 in Recessive Corpus Callosum Hypoplasia 2013 ·The American Journal of Human Genetics ·Naiara Akizu, (unknown), Tawfeg Ben‐Omran, Lailá Bastaki, Asma Al-Tawari, Maha S. Zaki, Roshan Koul, Emily Spencer, Rasim Özgür Rosti, Eric Scott, Elizabeth Nickerson, Stacey Gabriel, (unknown), Li Jiang, Matthew A. Deardorff, Laura K. Conlin, Margaret A. Horton, Elaine H. Zackai, Elliott H. Sherr, Joseph G. Gleeson	19
13	Improving surveillance for hyperammonemia in the newborn 2013 ·Molecular Genetics and Metabolism ·Samantha A. Schrier Vergano, (unknown), (unknown), (unknown), Matthew A. Deardorff, Neal Sondheimer	8
14	NIPBL rearrangements in Cornelia de Lange syndrome: evidence for replicative mechanism and genotype–phenotype correlation 2012 ·Genetics in Medicine ·Davut Pehli̇van, Melanie Hullings, Claudia M.B. Carvalho, Claudia Gonzaga‐Jauregui, Dorothy E. Loy, Laird G. Jackson, Ian D. Krantz, Matthew A. Deardorff, James R. Lupski	18
15	Investigation of autistic features among individuals with mild to moderate Cornelia de Lange syndrome 2012 ·American Journal of Medical Genetics Part A ·(unknown), Matthew A. Deardorff, Dinah Clark, Susan E. Levy, Ian D. Krantz, Mary Pipan	22
16	Neutral mitochondrial heteroplasmy and the influence of aging 2011 ·Human Molecular Genetics ·Neal Sondheimer, (unknown), (unknown), Matthew A. Deardorff, Abba Μ. Krieger, Håkon Håkonarson	73
17	Correction: Dosage Effects of Cohesin Regulatory Factor PDS5 on Mammalian Development: Implications for Cohesinopathies 2009 ·PLoS ONE ·Bin Zhang, Jufang Chang, M.W. Fu, Jie Huang, (unknown), (unknown), Sanjay K. Jain, Shashikant Kulkarni, Matthew A. Deardorff, Maria Luisa Giovannucci Uzielli, Dale Dorsett, David C. Beebe, Patrick Y. Jay, Robert O. Heuckeroth, Ian D. Krantz, Jeffrey Milbrandt	18
18	Dosage Effects of Cohesin Regulatory Factor PDS5 on Mammalian Development: Implications for Cohesinopathies 2009 ·PLoS ONE ·Bin Zhang, Jufang Chang, Ming Fu, Jie Huang, (unknown), (unknown), Sanjay Jain, (unknown), Matthew A. Deardorff, Maria Luisa Giovannucci Uzielli, Dale Dorsett, David C. Beebe, Patrick Y. Jay, Robert O. Heuckeroth, Ian D. Krantz, Jeffrey Milbrandt	68
19	A 781‐kb deletion of 13q12.3 in a patient with Peters plus syndrome 2009 ·American Journal of Medical Genetics Part A ·Chad Haldeman‐Englert, (unknown), Elizabeth A. Geiger, (unknown), Holly Feret, (unknown), (unknown), Matthew A. Deardorff, Elaine H. Zackai, Tamim H. Shaikh	15
20	The Human Bone Morphogenetic Protein 4 (BMP-4) Gene: Molecular Structure and Transcriptional Regulation 1998 ·Calcified Tissue International ·Eileen M. Shore, Meiqi Xu, Premal Shah, (unknown), Gregory V. Hahn, Matthew A. Deardorff, (unknown), Nancy B. Spinner, Michael Zasloff, John M. Wozney, Frederick S. Kaplan	43

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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