FS Collins

6.7k citations

50 papers · 2.2k indexed · 1 hit paper · h-index 25

Impact in

Hematology top 2%
- Acute Myeloid Leukemia Research
Genetics top 2%
- Hemoglobinopathies and Related Disorders

Papers in ⓘ

Hematology 17
- Acute Myeloid Leukemia Research 8
- Iron Metabolism and Disorders 5
Genetics 15
- Hemoglobinopathies and Related Disorders 13

Co-authors: A K Hajra (5 shared papers)Cisca Wijmenga (1 shared paper)David R. Engelke (1 shared paper)Susan A. Tarlé (3 shared papers)Thomas J. Sferra (1 shared paper)James Koh (1 shared paper)S M Weissman (2 shared papers)Todd A. Gray (2 shared papers)
Journals: Blood (16 papers)Nucleic Acids Research (3 papers)The American Journal of Human Genetics (2 papers)Journal of Biological Chemistry (2 papers)Proceedings of the National Academy of Sciences (2 papers)
Partner nations: United States Netherlands United Kingdom

In The Last Decade

FS Collins

49 papers receiving 2.1k citations

Hit Papers

align trajectories log scale

Cystic fibrosis: molecular biology and therapeutic implications 1992 · 638 citations

Peers

Countries citing papers authored by FS Collins

Since Specialization

Citations

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

Fields of papers citing papers by FS Collins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Cystic fibrosis: molecular biology and therapeutic implications Science ·FS Collins Hit paper breakdown →	1992	638
2	Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia [see comments] Blood ·PP Liu, A K Hajra, Cisca Wijmenga, FS Collins	1995	170
3	Phylogenetic footprinting reveals a nuclear protein which binds to silencer sequences in the human gamma and epsilon globin genes. Molecular and Cellular Biology ·Deborah L. Gumucio, Heidi Heilstedt-Williamson, Todd A. Gray, Susan A. Tarlé, David Shelton, Danilo A. Tagle, J L Slightom, M Goodman, FS Collins	1992	149
4	Direct sequencing of enzymatically amplified human genomic DNA. Proceedings of the National Academy of Sciences ·David R. Engelke, Patricia A. Hoener, FS Collins	1988	114
5	Menin Molecular Interactions: Insights into Normal Functions and Tumorigenesis Hormone and Metabolic Research ·Sunita Agarwal, P. A. Kennedy, Peter C. Scacheri, Elizabeth A. Novotny, A. B. Hickman, Aniello Cerrato, Terri Rice, J. Bernadette Moore, Somanhalli Girish Rao, Yuanyuan Ji, César Mateo, S. K. Libutti, Brian Oliver, Settara C. Chandrasekharappa, A. Lee Burns, FS Collins, Spiegel Am, Stephen J. Marx	2005	96
6	Characterization of the cystic fibrosis transmembrane conductance regulator promoter region. Chromatin context and tissue-specificity Journal of Biological Chemistry ·James Koh, Thomas J. Sferra, FS Collins	1993	76
7	Molecular characterization of 16p deletions associated with inversion 16 defines the critical fusion for leukemogenesis Blood ·Paula Marlton, David F. Claxton, P Liu, EH Estey, Miloslav Beran, Michelle M. LeBeau, JR Testa, FS Collins, JD Rowley, MJ Siciliano	1995	74
8	Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21. PubMed ·Diane E. Merry, J G Lesko, Donna M. Sosnoski, Richard A. Lewis, Mark Lubinsky, Barbara J. Trask, Ger van den Engh, FS Collins, Robert L. Nussbaum	1989	65
9	Analysis of the neurofibromatosis type 1 (NF1) GAP-related domain by site-directed mutagenesis. PubMed ·David H. Gutmann, Mark S. Boguski, Douglas A. Marchuk, Michael Wigler, FS Collins, Roymarie Ballester	1993	49
10	Interaction of Sp1 with the human gamma globin promoter: binding and transactivation of normal and mutant promoters Blood ·DL Gumucio, KL Rood, KL Blanchard-McQuate, TA Gray, AM Saulino, FS Collins	1991	48
11	The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focus. The American Journal of Human Genetics ·FS Collins, Ponder Ba, Seizinger Br, Epstein Cj	1989	44
12	Human fetal globin DNA sequences suggest novel conversion event Nucleic Acids Research ·Christian J. Stoeckert, FS Collins, S M Weissman	1984	43
13	Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron. The EMBO Journal ·James E. Metherall, FS Collins, J. Pan, S M Weissman, BG Forget	1986	40
14	Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population Blood ·FS Collins, CD Boehm, PG Waber, CJ Jr Stoeckert, S Weissman, BG Forget, HH Jr Kazazian	1984	38
15	The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobases Blood ·FS Collins, JL Cole, WK Lockwood, MC Iannuzzi	1987	38
16	Two frameshift mutations in the cystic fibrosis gene. PubMed ·M C Iannuzzi, Robert C. Stern, FS Collins, Catherine Tom Hon, Noriko Hidaka, Theresa V. Strong, Lore Becker, Mitchell L. Drumm, Marga Belle White, Bernard Gerrard	1991	38
17	Differential phylogenetic footprinting as a means to identify base changes responsible for recruitment of the anthropoid gamma gene to a fetal expression pattern. Journal of Biological Chemistry ·Deborah L. Gumucio, David Shelton, KL Blanchard-McQuate, Todd A. Gray, Susan A. Tarlé, Heidi Heilstedt-Williamson, J L Slightom, FS Collins, M. Goodman	1994	38
18	Interaction of Sp1 with the human gamma globin promoter: binding and transactivation of normal and mutant promoters Blood ·DL Gumucio, KL Rood, KL Blanchard-McQuate, TA Gray, AM Saulino, FS Collins	1991	37
19	Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks Blood ·PG Waber, MA Bender, RE Gelinas, C. Kattamis, A Karaklis, K. Sofroniadou, G. Stamatoyannopoulos, FS Collins, BG Forget, HH Jr Kazazian	1986	34
20	Identification of yeast artificial chromosomes containing the inversion 16 p-arm breakpoint associated with acute myelomonocytic leukemia Blood ·P Liu, David F. Claxton, Paula Marlton, A K Hajra, Julio C. Siciliano, Matthew L. Freedman, SC Chandrasekharappa, Kohsuke Yanagisawa, RL Stallings, FS Collins	1993	30

About FS Collins

FS Collins is a scholar working on Hematology, Genetics, Neurology, Molecular Biology and Genetics, having authored 50 papers that have together received 2.2k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (13 papers), Acute Myeloid Leukemia Research (8 papers), Iron Metabolism and Disorders (5 papers), Advanced biosensing and bioanalysis techniques (5 papers), Neurofibromatosis and Schwannoma Cases (5 papers), DNA and Nucleic Acid Chemistry (5 papers), RNA modifications and cancer (4 papers) and Cystic Fibrosis Research Advances (4 papers). The work is most often cited by research in Hematology (405 citations), Genetics (372 citations), Pulmonary and Respiratory Medicine (619 citations), Molecular Biology (1.1k citations) and Genetics (349 citations). FS Collins has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include A K Hajra, Cisca Wijmenga, David R. Engelke, Susan A. Tarlé, Thomas J. Sferra, James Koh, S M Weissman, Todd A. Gray, Deborah L. Gumucio and J L Slightom. Their work appears in journals such as Blood, Nucleic Acids Research, The American Journal of Human Genetics, Journal of Biological Chemistry and Proceedings of the National Academy of Sciences.

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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