Christin Collins

1.1k total citations
13 papers, 425 citations indexed

About

Christin Collins is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Christin Collins has authored 13 papers receiving a total of 425 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Epidemiology. Recurrent topics in Christin Collins's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Christin Collins is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Christin Collins collaborates with scholars based in United States, Italy and Netherlands. Christin Collins's co-authors include Madhuri Hegde, Alice Tanner, Lora Jh Bean, Cristina da Silva, Alessandra Ferlini, Jin‐Xiong She, Francesca Gualandi, Arunkanth Ankala, Richard McIndoe and Sarah Eckenrode and has published in prestigious journals such as Hepatology, Annals of Neurology and Annals of the New York Academy of Sciences.

In The Last Decade

Christin Collins

13 papers receiving 416 citations

Peers

Countries citing papers authored by Christin Collins

Since Specialization

Citations

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

Fields of papers citing papers by Christin Collins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christin Collins

This figure shows the co-authorship network connecting the top 25 collaborators of Christin Collins. A scholar is included among the top collaborators of Christin Collins 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 Christin Collins. Christin Collins is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	eP355: Repeat expansion disorders screening by genome sequencing: Strategy and stumbling blocks 2022 ·Genetics in Medicine ·(unknown), Abhinav Mathur, Ruby Liu, Christin Collins, Lora Jh Bean, Madhuri Hegde	1
2	Genetic basis of oculopharyngeal muscular dystrophy: detection of alanine repeats in PABPN1 gene by next generation sequencing 2021 ·Molecular Genetics and Metabolism ·Babi Ramesh Reddy Nallamilli, (unknown), Akanchha Kesari, Yang Wang, Christin Collins, Ruby Liu, (unknown), Abhinav Mathur, Lora Jh Bean, Madhuri Hegde	1
3	The role of clinical response to treatment in determining pathogenicity of genomic variants 2020 ·Genetics in Medicine ·Joseph Shen, Saskia B. Wortmann, Lonneke de Boer, Leo A. J. Kluijtmans, Marleen C.D.G. Huigen, Johannes Koch, (unknown), Christin Collins, Robin van der Lee, Clara van Karnebeek, Madhuri Hegde	10
4	15. A validation study of copy number variant (CNVs) detection to replace constitutional microarray from low resolution whole genome sequencing data 2018 ·Cancer Genetics ·Alka Chaubey, C. Alexander Valencia, Zeqiang Ma, Gerard P. Irzyk, (unknown), (unknown), Yang Wang, Alice Tanner, Christin Collins, Madhuri Hegde	1
5	Atypical presentation of neuronal ceroid lipofuscinosis type 8 in a sibling pair and review of the eye findings and neurological features 2016 ·American Journal of Ophthalmology Case Reports ·Rossana Sanchez Russo, Jiong Yan, Sarah Richards, Gary W. Mierau, Eric P. Wartchow, Christin Collins, Suma P. Shankar	5
6	Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis 2014 ·Molecular Autism ·Sek Won Kong, Mustafa Şahin, Christin Collins, Mary H. Wertz, Malcolm Campbell, (unknown), Dilja Krueger‐Burg, Mark F. Bear, Louis M. Kunkel, Isaac S. Kohane	15
7	A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield 2014 ·Annals of Neurology ·Arunkanth Ankala, Cristina da Silva, Francesca Gualandi, Alessandra Ferlini, Lora Jh Bean, Christin Collins, Alice Tanner, Madhuri Hegde	123
8	Molecular diagnostic testing for congenital disorders of glycosylation (CDG): Detection rate for single gene testing and next generation sequencing panel testing 2013 ·Molecular Genetics and Metabolism ·Melanie A. Jones, Devin Rhodenizer, Cristina da Silva, (unknown), Lisa M. Keong, Lora Jh Bean, Bradford Coffee, Christin Collins, Alice Tanner, Miao He, Madhuri Hegde	28
9	Comparative RNA editing in autistic and neurotypical cerebella 2012 ·Molecular Psychiatry ·Alal Eran, Jin Billy Li, (unknown), Jillian McCarthy, Fedik Rahimov, Christin Collins, Kyriacos Markianos, David Margulies, Emery N. Brown, Sarah E. Calvo, Isaac S. Kohane, Louis M. Kunkel	56
10	MCT8 Deficiency 2012 ·Journal of Child Neurology ·Davide Tonduti, Adeline Vanderver, Angela Berardinelli, Johanna Schmidt, Christin Collins, Francesca Novara, (unknown), (unknown), Fabio Triulzi, Janice Brunstrom-Hernandez, Orsetta Zuffardi, Umberto Balottin, Simona Orcesi	42
11	Lack of correlation between the levels of soluble cytotoxic T-lymphocyte associated antigen-4 (CTLA-4) and the CT-60 genotypes 2005 ·PubMed ·Sharad Purohit, Robert H. Podolsky, Christin Collins, Weipeng Zheng, Desmond Schatz, Andy Muir, Diane Hopkins, Yihua Huang, Jin‐Xiong She	50
12	Molecular Pathways Altered by Insulin B9‐23 Immunization 2004 ·Annals of the New York Academy of Sciences ·Sarah Eckenrode, Qingguo Ruan, Christin Collins, Ping Yang, Richard McIndoe, Andrew Muir, Jin‐Xiong She	7
13	Gene Expression Associated With Interferon Alfa Antiviral Activity in An Hcv Replicon Cell Line 2003 ·Hepatology ·Haizhen Zhu, Hongshan Zhao, Christin Collins, Sarah Eckenrode, (unknown), Richard McIndoe, James M. Crawford, David R. Nelson, Jin‐Xiong She, Chen Liu	86

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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