S. J. Hayflick

523 total citations
8 papers, 175 citations indexed

About

S. J. Hayflick is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, S. J. Hayflick has authored 8 papers receiving a total of 175 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Neurology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in S. J. Hayflick's work include Neurological diseases and metabolism (5 papers), Porphyrin Metabolism and Disorders (3 papers) and Hereditary Neurological Disorders (3 papers). S. J. Hayflick is often cited by papers focused on Neurological diseases and metabolism (5 papers), Porphyrin Metabolism and Disorders (3 papers) and Hereditary Neurological Disorders (3 papers). S. J. Hayflick collaborates with scholars based in United States, Netherlands and Italy. S. J. Hayflick's co-authors include Jane Gitschier, Kenneth N. Rosenbaum, Richard M. Pauli, Deborah A. Meyers, Theodore E. Whitmore, Susan J. Kirkpatrick, Donald W. Day, Ethylin Wang Jabs, Cathleen A. Coss and Rosalie Goldberg and has published in prestigious journals such as Journal of Clinical Investigation, Neurology and Journal of the Neurological Sciences.

In The Last Decade

S. J. Hayflick

7 papers receiving 172 citations

Peers

Countries citing papers authored by S. J. Hayflick

Since Specialization

Citations

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

Fields of papers citing papers by S. J. Hayflick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. J. Hayflick. 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 S. J. Hayflick. The network helps show where S. J. Hayflick may publish in the future.

Co-authorship network of co-authors of S. J. Hayflick

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

All Works

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8 of 8 papers shown

#	Work	Indexed citations
1	Coenzyme A protects against ferroptosis via CoAlation of mitochondrial thioredoxin reductase 2025 ·Journal of Clinical Investigation ·Chao‐Chieh Lin, Yi-Tzu Lin, (unknown), (unknown), (unknown), Denise Dunn, Taylor H. Nguyen, (unknown), (unknown), Lalitha Guruprasad, Erik J. Soderblom, Guofang Zhang, Chen‐Yong Lin, Valeriy Filonenko, Suh Young Jeong, Scott Floyd, S. J. Hayflick, Ivan Gout, Jen‐Tsan Chi	0
2	Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) - an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation 2013 ·Neuropediatrics ·(unknown), Ody C.M. Sibon, S. J. Hayflick, Tomasz Kmieć, Barbara Garavaglia, Valeria Tiranti, Boriana Büchner, Tobias B. Haack, Holger Prokisch, Thomas Meitinger, Thomas Klopstock	1
3	Spontaneous Murine Neuroaxonal Dystrophy: a Model of Infantile Neuroaxonal Dystrophy 2006 ·Journal of Comparative Pathology ·Donna M. Bouley, Jennifer J. McIntire, Brent T. Harris, Ravi Tolwani, Glen Otto, Rosemarie H. DeKruyff, S. J. Hayflick	17
4	A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect 2005 ·Neurogenetics ·Patrick Rump, (unknown), (unknown), P.M. Grootscholten, Johanna M. Fock, S. J. Hayflick, (unknown), Yvonne J. Vos, A. J. van Essen	14
5	Pantothenate kinase-associated neurodegeneration (formerly Hallervorden–Spatz Syndrome) 2003 ·Journal of the Neurological Sciences ·S. J. Hayflick	26
6	HARP syndrome is allelic with pantothenate kinase–associated neurodegeneration 2002 ·Neurology ·(unknown), (unknown), Jane Gitschier, (unknown), S. J. Hayflick	61
7	Fetal demise with Smith-Lemli-Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7-dehydrocholesterol ?7-reductase activity in chorionic villi 2000 ·Prenatal Diagnosis ·Leesa M. Linck, S. J. Hayflick, Don S. Lin, K.P. Battaile, (unknown), T. Burlingame, K. Michael Gibson, Maki Honda, Akira Honda, G Salen, G S Tint, W E Connor, Robert D. Steiner	28
8	Chromosomal deletion 4p15.32→p14 in a treacher collins syndrome patient: Exclusion of the disease locus from and mapping of anonymous DNA sequences to this region 1991 ·Genomics ·Ethylin Wang Jabs, Cathleen A. Coss, S. J. Hayflick, Theodore E. Whitmore, Richard M. Pauli, Susan J. Kirkpatrick, Deborah A. Meyers, Rosalie Goldberg, Donald W. Day, Kenneth N. Rosenbaum	28

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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