Caroline Andrews

6.0k total citations
60 papers, 2.8k citations indexed

About

Caroline Andrews is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Surgery. According to data from OpenAlex, Caroline Andrews has authored 60 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Pathology and Forensic Medicine, 11 papers in Molecular Biology and 10 papers in Surgery. Recurrent topics in Caroline Andrews's work include Ophthalmology and Eye Disorders (11 papers), Microtubule and mitosis dynamics (5 papers) and Pectus Deformity Diagnosis and Treatment (5 papers). Caroline Andrews is often cited by papers focused on Ophthalmology and Eye Disorders (11 papers), Microtubule and mitosis dynamics (5 papers) and Pectus Deformity Diagnosis and Treatment (5 papers). Caroline Andrews collaborates with scholars based in United States, United Kingdom and Saudi Arabia. Caroline Andrews's co-authors include Elizabeth C. Engle, Wai‐Man Chan, Scott K. Durum, Mairi H McLean, Nimit L. Patel, Irène Gottlob, Shery Thomas, Mervyn G. Thomas, Frank A. Proudlock and Kathleen M. George and has published in prestigious journals such as Advanced Materials, Nature Communications and Nature Genetics.

In The Last Decade

Caroline Andrews

58 papers receiving 2.7k citations

Peers

Countries citing papers authored by Caroline Andrews

Since Specialization

Citations

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

Fields of papers citing papers by Caroline Andrews

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Andrews

This figure shows the co-authorship network connecting the top 25 collaborators of Caroline Andrews. A scholar is included among the top collaborators of Caroline Andrews 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 Caroline Andrews. Caroline Andrews 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	IL-27 induces an IFN-like signature in murine macrophages which in turn modulate colonic epithelium 2023 ·Frontiers in Immunology ·Caroline Andrews, Mairi H McLean, Julie A. Hixon, Sergio M. Pontejo, Tregei Starr, Courtney S. Malo, Margaret C. Cam, Lisa A. Ridnour, Heather D. Hickman, Olivia Steele‐Mortimer, David A. Wink, Howard A. Young, Daniel W. McVicar, Wenqing Li, Scott K. Durum	6
2	Surface-fill hydrogel attenuates the oncogenic signature of complex anatomical surface cancer in a single application 2021 ·Nature Nanotechnology ·Poulami Majumder, (unknown), Ziqiu Wang, Kingshuk Dutta, Roma Pahwa, Liang Chen, Caroline Andrews, Nimit L. Patel, Junfeng Shi, Natalia de Val, Scott T.R. Walsh, Albert B. Jeon, Baktiar Karim, Chuong D. Hoang, Joel P. Schneider	71
3	Electrostatically Driven Guanidinium Interaction Domains that Control Hydrogel-Mediated Protein Delivery In Vivo 2019 ·ACS Central Science ·Stephen E. Miller, Yuji Yamada, Nimit L. Patel, Ernesto Suárez, Caroline Andrews, (unknown), Brian T. Luke, Raúl E. Cachau, Joel P. Schneider	31
4	New anti-IL-7Rα monoclonal antibodies show efficacy against T cell acute lymphoblastic leukemia in pre-clinical models 2019 ·Leukemia ·Julie A. Hixon, Caroline Andrews, (unknown), (unknown), Emilee Senkevitch, (unknown), João T. Barata, Wenqing Li, Joel P. Schneider, Scott T.R. Walsh, Scott K. Durum	26
5	Harmonising research outcomes for polycystic ovary syndrome: an international multi-stakeholder core outcome set 2019 ·Human Reproduction ·Bassel H. Al Wattar, Helena Teede, Rhonda Garad, Steve Franks, Adam Balen, Priya Bhide, Terhi Piltonen, Daniela Romualdi, Joop S.E. Laven, Mala Thondan, Aurora Bueno‐Cavanillas, Ngawai Moss, Caroline Andrews, Rachel Hawkes, Ben W. Mol, Khalid S. Khan, Shakila Thangaratinam	34
6	Tumour-elicited neutrophils engage mitochondrial metabolism to circumvent nutrient limitations and maintain immune suppression 2018 ·Nature Communications ·Christopher M. Rice, Luke C. Davies, Jeffrey Subleski, Nunziata Maio, Marieli Gonzalez-Cotto, Caroline Andrews, Nimit L. Patel, Erika M. Palmieri, Jonathan M. Weiss, Jungmin Lee, Christina M. Annunziata, Tracey A. Rouault, Scott K. Durum, Daniel W. McVicar	255
7	Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development 2015 ·American Journal of Medical Genetics Part A ·Mary C. Whitman, Caroline Andrews, Wai‐Man Chan, Max A. Tischfield, Steven F. Stasheff, Francesco Brancati, Xilma R. Ortiz‐González, Sara Nuovo, Francesco Garaci, Sarah MacKinnon, David G. Hunter, P. Ellen Grant, Elizabeth C. Engle	47
8	A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3 2013 ·Brain ·Sheena Chew, Ravikumar Balasubramanian, Wai‐Man Chan, Peter B. Kang, Caroline Andrews, Bryn D. Webb, Sarah MacKinnon, Darren T. Oystreck, Jessica K. Rankin, Thomas O. Crawford, Michael T. Geraghty, Scott L. Pomeroy, William F. Crowley, Ethylin Wang Jabs, David G. Hunter, P. Ellen Grant, Elizabeth C. Engle	81
9	Pontine Malformation, Undecussated Pyramidal Tracts, and Regional Polymicrogyria: A New Syndrome 2013 ·Pediatric Neurology ·(unknown), Yoshiaki Saito, Kenji Sugai, Eiji Nakagawa, (unknown), Hirofumi Komaki, Yasuhiro Nakata, Noriko Sato, (unknown), Toshiyuki Yamamoto, Wai‐Man Chan, Caroline Andrews, Elizabeth C. Engle, Masayuki Sasaki	6
10	Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation 2013 ·European Journal of Human Genetics ·Shery Thomas, Mervyn G. Thomas, Caroline Andrews, Wai‐Man Chan, Frank A. Proudlock, Rebecca J. McLean, (unknown), Elizabeth C. Engle, Irène Gottlob	42
11	RYR1Mutations as a Cause of Ophthalmoplegia, Facial Weakness, and Malignant Hyperthermia 2013 ·JAMA Ophthalmology ·Sherin Shaaban, Leigh Ramos‐Platt, Floyd H. Gilles, Wai‐Man Chan, Caroline Andrews, Umberto De Girolami, Joseph L. Demer, Elizabeth C. Engle	22
12	An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation 2012 ·Human Molecular Genetics ·G. Cederquist, Anna Łuchniak, Max A. Tischfield, (unknown), Yuyu Song, Manoj P. Menezes, Wai‐Man Chan, Caroline Andrews, Sheena Chew, Robyn V. Jamieson, Lavier Gomes, Maree Flaherty, P. Ellen Grant, Mohan L. Gupta, Elizabeth C. Engle	95
13	HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1 Mice 2012 ·The American Journal of Human Genetics ·Bryn D. Webb, Sherin Shaaban, Harald Gaspar, Luis F. Cunha, Christian Schubert, Ke Hao, Caroline D. Robson, Wai‐Man Chan, Caroline Andrews, Sarah MacKinnon, Darren T. Oystreck, David G. Hunter, Anthony J. Iacovelli, Xiaoqian Ye, (unknown), Elizabeth C. Engle, Ethylin Wang Jabs	53
14	HOXA1 mutations are not a common cause of Möbius syndrome 2010 ·Journal of American Association for Pediatric Ophthalmology and Strabismus ·Jessica K. Rankin, Caroline Andrews, Wai‐Man Chan, Elizabeth C. Engle	10
15	CHN1 mutations are not a common cause of sporadic Duane's retraction syndrome 2009 ·American Journal of Medical Genetics Part A ·Noriko Miyake, Caroline Andrews, (unknown), Wei He, Wai‐Man Chan, Elizabeth C. Engle	22
16	Magnetic resonance imaging of the endophenotype of a novel familial Möbius-like syndrome 2008 ·Journal of American Association for Pediatric Ophthalmology and Strabismus ·(unknown), Caroline Andrews, Wai‐Man Chan, Elizabeth C. Engle, Joseph L. Demer	12
17	Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features 2005 ·Blood Cells Molecules and Diseases ·Ronald L. Sham, Pradyumna D. Phatak, Carol West, Pauline Lee, Caroline Andrews, Ernest Beutler	93
18	Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development 2005 ·Nature Genetics ·Max A. Tischfield, Thomas M. Bosley, Mustafa A. Salih, Ibrahim A. Alorainy, Emin Cumhur Şener, Michael Nester, Darren T. Oystreck, Wai‐Man Chan, Caroline Andrews, Robert P. Erickson, Elizabeth C. Engle	206
19	Evidence for a Dual Mechanism for IL-10 Suppression of TNF-α Production That Does Not Involve Inhibition of p38 Mitogen-Activated Protein Kinase or NF-κB in Primary Human Macrophages 2002 ·The Journal of Immunology ·A Denys, Irina A. Udalova, Clive Smith, Lynn Williams, Cathleen J. Ciesielski, Jamie I. D. Campbell, Caroline Andrews, (unknown), Brian M. J. Foxwell	116
20	Duane Radial Ray Syndrome (Okihiro Syndrome) Maps to 20q13 and Results from Mutations in SALL4, a New Member of the SAL Family 2002 ·The American Journal of Human Genetics ·Raidah Albaradie, Koki Yamada, Cynthia St. Hilaire, Wai‐Man Chan, Caroline Andrews, Nathalie McIntosh, Motoi Nakano, (unknown), William R. Raymond, (unknown), Michael M. Okihiro, Elizabeth C. Engle	225

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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