Cara Skraban

1.2k total citations
31 papers, 244 citations indexed

About

Cara Skraban is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Cara Skraban has authored 31 papers receiving a total of 244 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 17 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in Cara Skraban's work include Genomics and Rare Diseases (14 papers), Congenital heart defects research (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Cara Skraban is often cited by papers focused on Genomics and Rare Diseases (14 papers), Congenital heart defects research (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Cara Skraban collaborates with scholars based in United States, United Kingdom and Australia. Cara Skraban's co-authors include Elaine H. Zackai, Emma Bedoukian, Kosuke Izumi, Stefan Rentas, Chris Feudtner, Fumin Lin, Matthew C. Dulik, K. Taylor Wild, Nancy B. Spinner and Emilie Lalonde and has published in prestigious journals such as PEDIATRICS, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Cara Skraban

27 papers receiving 243 citations

Peers

Countries citing papers authored by Cara Skraban

Since Specialization

Citations

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

Fields of papers citing papers by Cara Skraban

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cara Skraban

This figure shows the co-authorship network connecting the top 25 collaborators of Cara Skraban. A scholar is included among the top collaborators of Cara Skraban 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 Cara Skraban. Cara Skraban 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	Parents’ perceptions of the utility of genetic testing in the NICU 2025 ·Genetics in Medicine ·(unknown), Rebecca Mueller, Steven Joffe, Cara Skraban, Nancy B. Spinner, (unknown), Justin P. Clapp, David Munson, Chris Feudtner	2
3	How Neonatologists Use Genetic Information 2025 ·The Journal of Pediatrics ·(unknown), Rebecca Mueller, Steven Joffe, Cara Skraban, Nancy B. Spinner, (unknown), K. Taylor Wild, Justin T. Clapp, Chris Feudtner	0
4	Utility of genome sequencing in exome‐negative pediatric patients with neurodevelopmental phenotypes 2024 ·American Journal of Medical Genetics Part A ·Tomoki Nomakuchi, (unknown), Dong Li, (unknown), Holly Dubbs, Jacqueline Leonard, Colleen Muraresku, (unknown), (unknown), Amy Pizzino, Cara Skraban, Elaine H. Zackai, (unknown), Rebecca Ganetzky, Adeline Vanderver, Rebecca C. Ahrens‐Nicklas, Elizabeth Bhoj	0
5	Expanding the clinical phenotype and variant spectrum associated with RFX7 2024 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Christopher H. Gray, Cara Skraban, (unknown), (unknown), Ingo Helbig, Dong Li, Elizabeth Bhoj, Andrew K. Sobering	1
6	Expansion of the prenatal phenotype of Baraitser–Winter syndrome: Presentation of two cases of multiple congenital anomaly syndrome 2024 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Nahla Khalek, Shelly Soni, K. Taylor Wild, Cara Skraban, (unknown), (unknown), Edward R. Oliver, Emily A. Partridge, Sonika Agarwal, Allan G. B. Fisher, Jing Wang, Julie S. Moldenhauer	0
7	Retrospective identification of patients with SRRM2‐related neurodevelopmental disorder in a single tertiary children's hospital 2023 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Līvija Medne, Cara Skraban, (unknown), Christopher Gray, (unknown), (unknown), (unknown), Ian D. Krantz, Jill R. Murrell, Kosuke Izumi	3
8	CFAP45, a heterotaxy and congenital heart disease gene, affects cilia stability 2023 ·Developmental Biology ·Engin Deniz, (unknown), (unknown), (unknown), Weidong Ji, Monica Konstantino, (unknown), (unknown), Līvija Medne, Cara Skraban, Ian D. Krantz, Mustafa K. Khokha	7
9	Expanding the reproductive organ phenotype of CHD7‐spectrum disorder 2023 ·American Journal of Medical Genetics Part A ·Tomoki Nomakuchi, Melinda Danowitz, (unknown), Jacqueline Leonard, Kosuke Izumi, Ian D. Krantz, Thomas F. Kolon, David R. Langdon, Cara Skraban, Jason Van Batavia, Elaine H. Zackai, Kai Jiao, Rebecca L. Linn, (unknown), Mark R. Zaontz, Maria G. Vogiatzi, Louise C. Pyle	3
10	Diagnostic Yield of Exome Sequencing in Pediatric Cardiomyopathy 2023 ·The Journal of Pediatrics ·(unknown), Emma Bedoukian, Danielle S. Burstein, J. William Gaynor, Christopher Gray, Ian D. Krantz, Kosuke Izumi, Jacqueline Leonard, Kimberly Y. Lin, Līvija Medne, (unknown), Cara Skraban, (unknown), Rebecca C. Ahrens‐Nicklas	3
11	Molecular diagnosis and novel genes and phenotypes in a pediatric thoracic insufficiency cohort 2023 ·Scientific Reports ·Alanna Strong, Meckenzie Behr, (unknown), (unknown), Frank Mentch, Renata Pellegrino da Silva, Danielle Rux, Robert M. Campbell, Cara Skraban, Xiang Wang, Jason B. Anari, Benjamin P. Sinder, Patrick J. Cahill, Patrick Sleiman, Håkon Håkonarson	1
12	Co-Occurrence of Pallister-Killian Syndrome and Burkitt Lymphoma in a Patient with Near-Normal Neurocognitive Development 2023 ·Molecular Syndromology ·Kosuke Izumi, Rebecca Ganetzky, Gerald Wertheim, Cara Skraban, Emma Bedoukian, Alisha Wilkens, Christopher T. Fincher, Thomas Gilovich, Jill P. Ginsberg, Susan R. Rheingold, Laura K. Conlin, Matthew A. Deardorff	0
13	Genetics etiologies and genotype phenotype correlations in a cohort of individuals with central conducting lymphatic anomaly 2022 ·European Journal of Human Genetics ·(unknown), Christopher L. Smith, David M. Biko, Dong Li, Erin Pinto, (unknown), Cara Skraban, Elaine H. Zackai, Håkon Håkonarson, Yoav Dori, Sarah E. Sheppard	19
14	Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases 2022 ·The Journal of Pediatrics ·(unknown), K. Taylor Wild, Deborah McEldrew, Maninder Kaur, (unknown), Cara Skraban, Elaine H. Zackai, Līvija Medne, Kosuke Izumi, (unknown), (unknown), Tiffiney R. Hartman, (unknown), (unknown), Batsal Devkota, (unknown), Holly L. Hedrick, William H. Peranteau, Ian D. Krantz	3
15	How neonatologists use genetic testing: findings from a national survey 2021 ·Journal of Perinatology ·(unknown), John Flibotte, Cara Skraban, K. Taylor Wild, Steven Joffe, David Munson, Chris Feudtner	9
16	Expanding the phenotypic spectrum of Mendelian connective tissue disorders to include prominent kidney phenotypes 2021 ·American Journal of Medical Genetics Part A ·Alanna Strong, Cara Skraban, Kevin Meyers, Sandra Amaral, Susan L. Furth, Stacey Drant, (unknown), (unknown), Jessica I. Gold, Nina B. Gold, Jacqueline Leonard, (unknown), Elaine H. Zackai, Reed E. Pyeritz	1
17	Novel Missense CACNA1G Mutations Associated with Infantile-Onset Developmental and Epileptic Encephalopathy 2020 ·International Journal of Molecular Sciences ·Géza Berecki, Katherine L. Helbig, Tyson L. Ware, Bronwyn E. Grinton, Cara Skraban, Eric D. Marsh, Samuel F. Berkovic, Steven Petrou	10
18	Ciliopathies: Coloring outside of the lines 2020 ·American Journal of Medical Genetics Part A ·Alanna Strong, Dong Li, Frank Mentch, Emma Bedoukian, Erum A. Hartung, Kevin Meyers, Cara Skraban, Jessica Wen, Līvija Medne, Joseph Glessner, Deborah Watson, Ian D. Krantz, Håkon Håkonarson	7
19	Genomic Diagnosis for Pediatric Disorders: Revolution and Evolution 2020 ·Frontiers in Pediatrics ·Emilie Lalonde, Stefan Rentas, Fumin Lin, Matthew C. Dulik, Cara Skraban, Nancy B. Spinner	30
20	Clinical utility of exome sequencing in infantile heart failure 2019 ·Genetics in Medicine ·Alyssa Ritter, Emma Bedoukian, Justin H. Berger, (unknown), Christopher Gray, Ian D. Krantz, Kosuke Izumi, Jane Juusola, Jacqueline Leonard, Kimberly Y. Lin, Līvija Medne, Avni Santani, Cara Skraban, Sandra Yang, Rebecca C. Ahrens‐Nicklas	13

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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