Daryl A. Scott

10.8k citations

97 papers · 3.9k indexed · h-index 32

Impact in

Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
Otorhinolaryngology top 1%
- Ear Surgery and Otitis Media

Papers in

Sensory Systems 12
- Hearing, Cochlea, Tinnitus, Genetics 12
Genetics 40
- Genomic variations and chromosomal abnormalities 20
- Genetics and Neurodevelopmental Disorders 9

Co-authors: Lawrence P. Karniski Val C. Sheffield Rong Wang Dick Tibboel Annelies de Klein Ashley M. Holder Sau Wai Cheung Yong Tang
Journals: Human Molecular Genetics (7 papers)PLoS ONE (5 papers)European Journal of Human Genetics (4 papers)Journal of Medical Genetics (4 papers)American Journal of Medical Genetics Part A (34 papers)
Partner nations: United States Netherlands Germany

In The Last Decade

Daryl A. Scott

93 papers receiving 3.8k citations

Peers

Countries citing papers authored by Daryl A. Scott

Since Specialization

Citations

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

Fields of papers citing papers by Daryl A. Scott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Daryl A. Scott, 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 Daryl A. Scott Line = papers co-authored together Daryl A. Scott links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Dominant Negative Variants in IKZF2 Cause ICHAD Syndrome, a New Disorder Characterized by Immunodysregulation, Craniofacial Anomalies, Hearing Impairment, Athelia, and Developmental Delay Clinical Immunology ·Maryam Vaseghi‐Shanjani, Arezoo Mohajeri, Jill A. Rosenfeld, Henry Y. Lu, Mehul Sharma, Seema R. Lalani, Sarah K. Nicholas, Daryl A. Scott, Stuart E. Turvey, Anna Lehman	2023	1
2	Integrative analysis of transcriptome dynamics during human craniofacial development identifies candidate disease genes Nature Communications ·Saeid Mashhadi, Cecilia Delgado-Montemayor, Stefani Yultrian, Andrea Wilderman, Kelsey Robinson, 義博二五, Jill A. Rosenfeld, Jennifer VanOudenhove, Daryl A. Scott, Elizabeth J. Leslie, Justin Cotney	2023	14
3	SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2 Human Molecular Genetics ·Andrés Hernández, Katherine E. Pendleton, Sangbae Kim, Yumei Li, Bum Joon Kim, Hitisha P. Zaveri, Valerie K. Jordan, Jérôme Leclerc-Loiselle, M. Cecilia Ljungberg, Rui Chen, Rainer B. Lanz, Daryl A. Scott	2023	1
4	Early initiation of B‐vitamin supplementation may reduce symptoms and explain intrafamilial variability: Insights from two sibling pairs from the TANGO2 natural history study American Journal of Medical Genetics Part A ·Christina Y. Miyake, Savvas Manikas, Lilei Zhang, Patricia Bau, Mahshid S. Azamian, Daryl A. Scott, Andrés Hernández, Seema R. Lalani	2023	7
5	Underlying genetic etiologies of congenital diaphragmatic hernia Prenatal Diagnosis ·Daryl A. Scott, Yanli Li, Jérôme Leclerc-Loiselle, Wuyang Shi	2022	8
6	Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans American Journal of Medical Genetics Part A ·Yanli Li, Сейтниязов Кошкарбай Матенович, Keren Machol, Sundeep G. Keswani, Lorraine Potocki, Eleonora Di Gregorio, D Franzen, Alfredo Brusco, Andrés Hernández, Daryl A. Scott	2021	7
7	Clinical exome sequencing data reveal high diagnostic yields for congenital diaphragmatic hernia plus (CDH+) and new phenotypic expansions involving CDH Journal of Medical Genetics ·Subramaniam Sundaramahalingam, Ian M. Campbell, Andrés Hernández, Seema R. Lalani, Pengfei Liu, Chad A. Shaw, Jill A. Rosenfeld, Daryl A. Scott	2021	21
8	Congenital diaphragmatic hernia as a prominent feature of a SPECC1L‐related syndrome American Journal of Medical Genetics Part A ·K. Taylor Wild, 義博二五, Elizabeth Bhoj, Haowei Du, Shalini N. Jhangiani, Jennifer E. Posey, James R. Lupski, Daryl A. Scott, Elaine H. Zackai	2020	6
9	Recessive ACO2 variants as a cause of isolated ophthalmologic phenotypes American Journal of Medical Genetics Part A ·E.V. Korotkikh, Mahshid S. Azamian, Seema R. Lalani, Kimberly G. Yen, V. Reid Sutton, Daryl A. Scott	2020	6
10	Patterns of co-occurring birth defects among infants with hypospadias Journal of Pediatric Urology ·Stylianos Grigorakis, Renata H. Benjamin, SOO LIN GEH, Scott McLean, Hope Northrup, Laura E. Mitchell, Peter H. Langlois, Mark A. Canfield, Angela E. Scheuerle, Daryl A. Scott, Christian P. Schaaf, Joseph W. Ray, Chip Pearson, Han Chen, Michael D. Swartz, Philip J. Lupo, A. J. Agopian	2020	2
11	RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects Disease Models & Mechanisms ·Bum‐Joon Kim, Hitisha P. Zaveri, Valerie K. Jordan, Andrés Hernández, Canli Yuan, Karen Alejandra Miranda-Fernández, Wei Yu, Robert J. Schwartz, Daryl A. Scott	2018	7
12	SOX7 expression is critically required in FLK1-expressing cells for vasculogenesis and angiogenesis during mouse embryonic development Mechanisms of Development ·Andrew J. Lilly, 문성우, Daryl A. Scott, Georges Lacaud, Valérie Kouskoff	2017	22
13	FBN1 contributing to familial congenital diaphragmatic hernia American Journal of Medical Genetics Part A ·T. Beck, Philippe M. Campeau, Shalini N. Jhangiani, Tomasz Gambin, Alexander Li, Reem Abo‐Zahrah, Valerie K. Jordan, Andrés Hernández, Wojciech Wiszniewski, Donna M. Muzny, Richard A. Gibbs, Eric Boerwinkle, James R. Lupski, Brendan Lee, William Reardon, Daryl A. Scott	2015	23
14	VACTERL Association Etiology: The Impact of de novo and Rare Copy Number Variations Molecular Syndromology ·Erwin Brosens, H. J. Eussen, Yolande van Bever, R.M. van der Helm, Hanneke IJsselstijn, Hitisha P. Zaveri, René Wijnen, Daryl A. Scott, Dick Tibboel, Annelies de Klein	2012	22
15	Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage–fusion–bridge for telomere stabilization Human Genetics ·Svetlana A. Yatsenko, Patricia Hixson, Erin K. Roney, Daryl A. Scott, Christian P. Schaaf, Yu‐Tze Ng, Randi T. Sachs, Richard B. Fisher, Ankita Patel, Sau Wai Cheung, James R. Lupski	2012	31
16	Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia Journal of Medical Genetics ·Margaret Wat, Danielle Veenma, Jacob S. Hogue, Ashley M. Holder, Zhou Yunlu, Mayumi Matsukawa, Neil A. Hanchard, 韩策, Caraciolo J. Fernandes, Anthony E. Johnson, Kevin P. Lally, Anne Slavotinek, Olivier Danhaive, T Schaible, S.W. Cheung, Katherine A. Rauen, Vijay S. Tonk, Dick Tibboel, Annelies de Klein, Daryl A. Scott	2011	65
17	Delineation of a 1.65 Mb critical region for hemihyperplasia and digital anomalies on Xq25 American Journal of Medical Genetics Part A ·Nicholas Andrew Fernandes, Ronald O. Smith, Ping Fang, Erin K. Roney, Sau Wai Cheung, Daryl A. Scott	2010	4
18	Deletions of Xp provide evidence for the role of holocytochrome C‐type synthase (HCCS) in congenital diaphragmatic hernia American Journal of Medical Genetics Part A ·Katrin Wöllert, David Pearson, Gayle Patel, Barbara R. Pober, LaDonna Immken, Sau Wai Cheung, Daryl A. Scott	2010	14
19	Ovotestes and XY sex reversal in a female with an interstitial 9q33.3‐q34.1 deletion encompassing NR5A1 and LMX1B causing features of genitopatellar syndrome American Journal of Medical Genetics Part A ·Silke Schlaubitz, Svetlana A. Yatsenko, Laurie D. Smith, Kory Keller, Lisenka E.L.M. Vissers, Daryl A. Scott, Wei Cai, William Reardon, Omar Abdul‐Rahman, Edward J. Lammer, Amrullah Awsar, Ellen Magenis, Joris A. Veltman, Paweł Stankiewicz, Bernhard Zabel, Brendan Lee	2007	38
20	WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH American Journal of Medical Genetics Part A ·Patrick A. Lennon, Daryl A. Scott, O. Gedik, David S. Wargowski, Susan J. Kirkpatrick, Ankita Patel, Sau Wai Cheung	2006	9

About Daryl A. Scott

Daryl A. Scott is a scholar working on Sensory Systems, Genetics, Genetics, Molecular Biology and Surgery, having authored 97 papers that have together received 3.9k indexed citations. Recurring topics across this work include Congenital heart defects research (23 papers), Congenital Diaphragmatic Hernia Studies (20 papers), Genomic variations and chromosomal abnormalities (20 papers), Tracheal and airway disorders (14 papers), RNA modifications and cancer (14 papers), Hearing, Cochlea, Tinnitus, Genetics (12 papers), Congenital Anomalies and Fetal Surgery (10 papers) and Genetics and Neurodevelopmental Disorders (9 papers). The work is most often cited by research in Sensory Systems (842 citations), Otorhinolaryngology (316 citations), Neurology (464 citations), Genetics (1.0k citations) and Molecular Biology (1.9k citations). Daryl A. Scott has collaborated with scholars based in United States, Netherlands and Germany. Frequent co-authors include Lawrence P. Karniski, Val C. Sheffield, Rong Wang, Dick Tibboel, Annelies de Klein, Ashley M. Holder, Sau Wai Cheung, Yong Tang, Xiaoyan Tian and Suzanne L. Mansour. Their work appears in journals such as Human Molecular Genetics, PLoS ONE, European Journal of Human Genetics, Journal of Medical Genetics and American Journal of Medical Genetics Part A.

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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