M. Litt

2.4k total citations · 1 hit paper
16 papers, 1.6k citations indexed

About

M. Litt is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, M. Litt has authored 16 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in M. Litt's work include DNA Repair Mechanisms (4 papers), RNA regulation and disease (3 papers) and RNA modifications and cancer (3 papers). M. Litt is often cited by papers focused on DNA Repair Mechanisms (4 papers), RNA regulation and disease (3 papers) and RNA modifications and cancer (3 papers). M. Litt collaborates with scholars based in United States, United Kingdom and South Africa. M. Litt's co-authors include J.A. Luty, R.E. Magenis, Olivier Civelli, Qun‐Yong Zhou, D.L. Browne, Leland Allen, David K. Grandy, Michael R. Condon, Markku Kurkinen and Robert R. Sheehy and has published in prestigious journals such as Nucleic Acids Research, Human Molecular Genetics and Journal of Investigative Dermatology.

In The Last Decade

M. Litt

15 papers receiving 1.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene.

1989 1.4k citations M. Litt, J.A. Luty PubMed profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
M. Litt United States	9	827	758	527	99	98	16	1.6k
J.A. Luty United States	7	895 1.1×	782 1.0×	546 1.0×	90 0.9×	69 0.7×	8	1.6k
Joyce Miller United States	9	768 0.9×	865 1.1×	707 1.3×	90 0.9×	80 0.8×	10	1.7k
Joan C. Menninger United States	22	778 0.9×	958 1.3×	238 0.5×	94 0.9×	105 1.1×	27	1.6k
Janet Ziegle United States	17	894 1.1×	588 0.8×	380 0.7×	59 0.6×	87 0.9×	28	1.6k
John W. Fondon United States	16	557 0.7×	1.1k 1.5×	281 0.5×	103 1.0×	170 1.7×	19	1.7k
Martin Goodson United Kingdom	7	831 1.0×	1.5k 1.9×	424 0.8×	72 0.7×	65 0.7×	10	2.0k
Fernando Pardo-Manuel de Villena United States	21	1.1k 1.3×	922 1.2×	320 0.6×	73 0.7×	87 0.9×	37	1.8k
Iris L. Gonzalez United States	23	372 0.4×	1.7k 2.2×	313 0.6×	68 0.7×	107 1.1×	37	2.2k
Cornelia Schmidt Germany	21	459 0.6×	657 0.9×	173 0.3×	80 0.8×	50 0.5×	42	1.2k
Robert A. Rollins United States	16	394 0.5×	1.3k 1.7×	264 0.5×	90 0.9×	33 0.3×	21	1.7k

Countries citing papers authored by M. Litt

Since Specialization

Citations

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

Fields of papers citing papers by M. Litt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Litt

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

All Works

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16 of 16 papers shown

Taylor, Todd D., Susan J. Hayflick, M. Litt, et al.. (1998). Confirmation of Linkage of Clouston Syndrome (Hidrotic Ectodermal Dysplasia) to 13q11-q12.1 with Evidence for Multiple Independent Mutations. Journal of Investigative Dermatology. 111(1). 83–85. 14 indexed citations

Hayflick, Susan J., Todd D. Taylor, Wendy McKinnon, et al.. (1996). Clouston Syndrome (Hidrotic Ectodermal Dysplasia) Is Not Linked to Keratin Gene Clusters on Chromosomes 12 and 17. Journal of Investigative Dermatology. 107(1). 11–14. 6 indexed citations

Litt, M. & D.L. Browne. (1994). Characterization of (CA)_n Microsatellite Repeats from Large‐Insert Clones. Current Protocols in Human Genetics. 0(1). Unit 2.4–Unit 2.4. 2 indexed citations

Browne, D.L., Veronica van Heyningen, Wendy A. Bickmore, & M. Litt. (1993). Dinucleotide repeat polymorphism at the D11S995 locus. Human Molecular Genetics. 2(8). 1332–1332.

Jensen, Steven, Rosemarie Plaetke, John Holik, et al.. (1993). Linkage Analysis of Schizophrenia: The D1 Dopamine Receptor Gene and Several Flanking DNA Markers. Human Heredity. 43(1). 58–62. 12 indexed citations

Browne, D.L., et al.. (1993). Tetranucleotide repeat polymorphism at the D11S488 locus. Human Molecular Genetics. 2(1). 89–89. 14 indexed citations

Browne, D.L., et al.. (1993). Dinucleotide repeat polymorphism at the KCNA5 locus. Human Molecular Genetics. 2(9). 1512–1512. 8 indexed citations

Gelernter, Joel, A.J. Pakstis, David K. Grandy, et al.. (1992). Linkage map of eight human chromosome 11q markers, including DRD2, spanning 60 cM. Cytogenetic and Genome Research. 60(1). 26–28. 6 indexed citations

Browne, D.L., J. Zonana, & M. Litt. (1991). Dinucleotide repeat polymorphism at the PGK1 locus. Nucleic Acids Research. 19(7). 1721–1721. 10 indexed citations

10.

Maslen, Cheryl L., et al.. (1991). A BamHI polymorphism at the fibrillin (FBN) locus. Nucleic Acids Research. 19(15). 4309–4309. 4 indexed citations

11.

Grandy, David K., Qun‐Yong Zhou, Leland Allen, et al.. (1990). A human D1 dopamine receptor gene is located on chromosome 5 at q35.1 and identifies an EcoRI RFLP.. PubMed. 47(5). 828–34. 55 indexed citations

12.

Litt, M. & J.A. Luty. (1989). A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene.. PubMed. 44(3). 397–401. 1385 indexed citations breakdown →

13.

Litt, M.. (1989). Localization of a human brain sodium channel gene (SCN2A) to chromosome 2. Genomics. 5(2). 204–208. 30 indexed citations

14.

Boyd, C. D., Inder Gadi, M. Litt, et al.. (1988). The genes coding for human pro alpha 1(IV) collagen and pro alpha 2(IV) collagen are both located at the end of the long arm of chromosome 13.. PubMed. 42(2). 309–14. 33 indexed citations

15.

Litt, M., G.A.P. Bruns, Robert R. Sheehy, & R.E. Magenis. (1986). A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37.. PubMed. 38(3). 288–96. 9 indexed citations

16.

Litt, M., Robert R. Sheehy, G.A.P. Bruns, & R.E. Magenis. (1986). A polymorphic locus on the long arm of chromosome 20 defined by two probes from a single cosmid. Human Genetics. 73(4). 340–345. 4 indexed citations

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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