Matthew A. Deardorff

11.1k citations

109 papers · 3.6k indexed · h-index 32

Genetics top 1%
- Genomic variations and chromosomal abnormalities 16
- Genetic Syndromes and Imprinting 15
- Genomics and Rare Diseases 9
Molecular Biology top 2%
- Genomics and Chromatin Dynamics 24
- Cancer-related gene regulation 11
- Epigenetics and DNA Methylation 11
- Wnt/β-catenin signaling in development and cancer 9
Developmental Biology top 5%
Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics 13
Cell Biology top 5%

Co-authors: Peter S. Klein Ian D. Krantz Change Tan Elaine H. Zackai Nancy B. Spinner Laura K. Conlin Håkon Håkonarson Maninder Kaur
Cited by: Genetics Molecular Biology Developmental Biology
Journals: American Journal of Medical Genetics Part C Seminars in Medical Genetics (4 papers)American Journal of Medical Genetics Part A (35 papers)Human Molecular Genetics (3 papers)
Partner nations: United States Canada Italy

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

The 25 scholars most cited alongside Matthew A. Deardorff, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Matthew A. Deardorff Line = papers co-authored together Matthew A. Deardorff links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	16q24.3 Microdeletions Disrupting Upstream Non-Coding Region of ANKRD11 Cause KBG Syndrome Genes ·Aiko Iwata‐Otsubo,Christopher Andrews,Jorune Balciuniene,Н.В. Грисенко,Qiming Zhang,Teoría De Grupos,Cara Skraban,Christopher Gray,Elaine H. Zackai,Holly Dubbs,Matthew A. Deardorff,Laura K. Conlin,Kosuke Izumi	2025	1
2	Autonomous drone behavior via MCDM of UFOMap layers 篠田榮,I. I. SEREBRENNIKOV,А.С. Самойлов,徐川梅,Matthew A. Deardorff,Derek T. Anderson,Robert H. Luke	2024	0
3	Improving Real-Time Aerial 3D Reconstruction: Towards Fusion of a Hand-Crafted SfM Algorithm with a Data-Driven Deep Neural Network А.С. Самойлов,I. I. SEREBRENNIKOV,Derek T. Anderson,James M. Keller,徐川梅,Matthew A. Deardorff,Robert Luke	2023	0
4	The chromatin remodeler ISWI acts during Drosophila development to regulate adult sleep Science Advances ·Naihua N. Gong,Marc Augustin,Vesna Sabol,Emilia H. Moscato,Milán Szuperák,Qin Wang,Matthew Jensen,Santhosh Girirajan,Tiong Yang Tan,Matthew A. Deardorff,Dong Li,Yuanquan Song,Matthew S. Kayser	2021	9
5	A novel pathogenic missense ADAMTS17 variant that impairs secretion causes Weill-Marchesani Syndrome with variably dysmorphic hand features Scientific Reports ·日本社会党中央本部,Jane S. Green,Somayyeh Fahiminiya,Jacek Majewski,Bridget A. Fernandez,Matthew A. Deardorff,(unknown),Alicia Vanessa Ceballos Salinas,Dirk Hubmacher,Suneel Apte,Kym M. Boycott,Dennis E. Bulman,David A. Dyment,洗介福士,Michael Brudno,Michael O. Woods	2020	14
6	Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach European Journal of Human Genetics ·Chao Wu,Batsal Devkota,Perry Evans,Xiaonan Zhao,Samuel W. Baker,Sergei B. Kashevsky,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	2019	10
7	TRPV6 Variants Interfere with Maternal-Fetal Calcium Transport through the Placenta and Cause Transient Neonatal Hyperparathyroidism The American Journal of Human Genetics ·Yoshiro Suzuki,David Chitayat,Hirotake Sawada,Matthew A. Deardorff,Heather M. McLaughlin,Amber Begtrup,Sekii Takahiro,Jennifer Harrington,Karen Chong,Maian Roifman,Katheryn Grand,Makoto Tominaga,Fumio Takada,K. C. Chen,Dong Seop Park,H. Mutoh,Shawn D. Whitacre,Gen Nishimura	2018	54
8	The utility of alpha‐fetoprotein screening in Beckwith–Wiedemann syndrome American Journal of Medical Genetics Part A ·Kelly A. Duffy,Matthew A. Deardorff,Jennifer M. Kalish	2017	13
9	Fetal akinesia deformation sequence due to a congenital disorder of glycosylation American Journal of Medical Genetics Part A ·Rebecca Ganetzky,Kosuke Izumi,Andrew C. Edmondson,Colleen Muraresku,Elaine H. Zackai,Matthew A. Deardorff,Jaya Ganesh	2015	11
10	Mutations in the ABCC6 Gene as a Cause of Generalized Arterial Calcification of Infancy: Genotypic Overlap with Pseudoxanthoma Elasticum 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	2013	59
11	Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low‐Level Uniparental Disomy American Journal of Medical Genetics Part A ·Jennifer M. Kalish,Laura K. Conlin,Sogol Mostoufi‐Moab,Alisha Wilkens,Surabhi Mulchandani,Kristin Zelley,Wilson Moreno León,Tricia Bhatti,Pierre Russo,Peter Mattei,William G. Mackenzie,Virginia A. LiVolsi,Kim E. Nichols,Jaclyn A. Biegel,Nancy B. Spinner,Matthew A. Deardorff	2013	15
12	Whole-Exome Sequencing Identifies Mutated C12orf57 in Recessive Corpus Callosum Hypoplasia The American Journal of Human Genetics ·Naiara Akizu,MO Yehe,Tawfeg Ben‐Omran,Lailá Bastaki,Asma Al-Tawari,Maha S. Zaki,Roshan Koul,Emily Spencer,Rasim Özgür Rosti,Eric Scott,Elizabeth Nickerson,Stacey Gabriel,Hyun Woong Chang,Li Jiang,Matthew A. Deardorff,Laura K. Conlin,Margaret A. Horton,Elaine H. Zackai,Elliott H. Sherr,Joseph G. Gleeson	2013	19
13	Improving surveillance for hyperammonemia in the newborn Molecular Genetics and Metabolism ·Samantha A. Schrier Vergano,Maggi C. Miller,Bin He,Christina M Pabelick,Matthew A. Deardorff,Neal Sondheimer	2013	8
14	NIPBL rearrangements in Cornelia de Lange syndrome: evidence for replicative mechanism and genotype–phenotype correlation 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	2012	18
15	Investigation of autistic features among individuals with mild to moderate Cornelia de Lange syndrome American Journal of Medical Genetics Part A ·John T. Jeremko,Matthew A. Deardorff,Dinah Clark,Susan E. Levy,Ian D. Krantz,Mary Pipan	2012	22
16	Neutral mitochondrial heteroplasmy and the influence of aging Human Molecular Genetics ·Neal Sondheimer,José Gustavo,M. T. Suárez,Matthew A. Deardorff,Abba Μ. Krieger,Håkon Håkonarson	2011	73
17	Correction: Dosage Effects of Cohesin Regulatory Factor PDS5 on Mammalian Development: Implications for Cohesinopathies PLoS ONE ·Bin Zhang,Jufang Chang,M.W. Fu,Jie Huang,Mihaela Maria Similie,齐东亮,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	2009	18
18	Dosage Effects of Cohesin Regulatory Factor PDS5 on Mammalian Development: Implications for Cohesinopathies PLoS ONE ·Bin Zhang,Jufang Chang,Ming Fu,Jie Huang,Mihaela Maria Similie,齐东亮,Sanjay Jain,孝二真崎,Matthew A. Deardorff,Maria Luisa Giovannucci Uzielli,Dale Dorsett,David C. Beebe,Patrick Y. Jay,Robert O. Heuckeroth,Ian D. Krantz,Jeffrey Milbrandt	2009	68
19	A 781‐kb deletion of 13q12.3 in a patient with Peters plus syndrome American Journal of Medical Genetics Part A ·Chad Haldeman‐Englert,Janusz Lichtarski,Elizabeth A. Geiger,james dabbs,Holly Feret,Yusra kareem,H. J. Laméris,Matthew A. Deardorff,Elaine H. Zackai,Tamim H. Shaikh	2009	15
20	The Human Bone Morphogenetic Protein 4 (BMP-4) Gene: Molecular Structure and Transcriptional Regulation Calcified Tissue International ·Eileen M. Shore,Meiqi Xu,Premal Shah,PAOLA CAIOZZO,Gregory V. Hahn,Matthew A. Deardorff,Fu-Min Chen,Nancy B. Spinner,Michael Zasloff,John M. Wozney,Frederick S. Kaplan	1998	43

About Matthew A. Deardorff

Matthew A. Deardorff is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 109 papers that have together received 3.6k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (24 papers), Genomic variations and chromosomal abnormalities (16 papers), Genetic Syndromes and Imprinting (15 papers), Prenatal Screening and Diagnostics (13 papers), Cancer-related gene regulation (11 papers), Epigenetics and DNA Methylation (11 papers), Genomics and Rare Diseases (9 papers) and Wnt/β-catenin signaling in development and cancer (9 papers). The work is most often cited by research in Genetics (1.4k citations), Molecular Biology (2.7k citations) and Developmental Biology (69 citations). Matthew A. Deardorff has collaborated with scholars based in United States, Canada and Italy. Frequent 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. Their work appears in journals such as American Journal of Medical Genetics Part C Seminars in Medical Genetics, American Journal of Medical Genetics Part A, Human Molecular Genetics, Genetics in Medicine and The American Journal of Human Genetics.

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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