Mark Lipson

13.8k total citations · 1 hit paper
62 papers, 2.4k citations indexed

About

Mark Lipson is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Mark Lipson has authored 62 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 21 papers in Molecular Biology and 13 papers in Clinical Biochemistry. Recurrent topics in Mark Lipson's work include Forensic and Genetic Research (15 papers), Metabolism and Genetic Disorders (13 papers) and Forensic Anthropology and Bioarchaeology Studies (7 papers). Mark Lipson is often cited by papers focused on Forensic and Genetic Research (15 papers), Metabolism and Genetic Disorders (13 papers) and Forensic Anthropology and Bioarchaeology Studies (7 papers). Mark Lipson collaborates with scholars based in United States, Canada and Germany. Mark Lipson's co-authors include David Reich, Bonnie Berger, Po‐Ru Loh, Priya Moorjani, Nick Patterson, Joseph K. Pickrell, Nick Patterson, Mark Stoneking, Kumarasamy Thangaraj and Brigitte Pakendorf and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Mark Lipson

61 papers receiving 2.3k 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.

Inferring Admixture Histories of Human Populations Using Linkage Disequilibrium

2013 272 citations Po‐Ru Loh, Mark Lipson et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mark Lipson United States	26	1.2k	906	475	216	203	62	2.4k
Marja‐Liisa Savontaus Finland	25	973 0.8×	1.4k 1.5×	482 1.0×	237 1.1×	125 0.6×	53	2.6k
Maria João Prata Portugal	27	1.3k 1.1×	837 0.9×	94 0.2×	353 1.6×	151 0.7×	119	2.4k
Kirsi Huoponen Finland	27	919 0.8×	2.2k 2.4×	938 2.0×	255 1.2×	121 0.6×	49	3.4k
Päivi Lahermo Finland	26	1.3k 1.1×	1.1k 1.2×	73 0.2×	243 1.1×	97 0.5×	32	2.5k
Doron M. Behar Israel	25	1.9k 1.6×	1.0k 1.1×	133 0.3×	723 3.3×	160 0.8×	62	3.2k
Qing‐Peng Kong China	36	1.6k 1.3×	2.3k 2.5×	426 0.9×	548 2.5×	31 0.2×	111	3.8k
Martin Brandon United States	9	897 0.7×	2.4k 2.7×	732 1.5×	134 0.6×	55 0.3×	9	3.1k
S.S. Papiha United Kingdom	22	1.7k 1.4×	728 0.8×	73 0.2×	517 2.4×	47 0.2×	117	2.7k
Shay Tzur Israel	23	812 0.7×	738 0.8×	64 0.1×	178 0.8×	41 0.2×	44	2.2k
Ronald J. Trent Australia	32	1.1k 0.9×	1.4k 1.5×	42 0.1×	54 0.3×	138 0.7×	162	4.8k

Countries citing papers authored by Mark Lipson

Since Specialization

Citations

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

Fields of papers citing papers by Mark Lipson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Lipson

This figure shows the co-authorship network connecting the top 25 collaborators of Mark Lipson. A scholar is included among the top collaborators of Mark Lipson 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 Mark Lipson. Mark Lipson 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

Lipson, Mark, Harald Ringbauer, Giulio Lucarini, et al.. (2025). High continuity of forager ancestry in the Neolithic period of the eastern Maghreb. Nature. 641(8064). 925–931. 1 indexed citations

Bachmann, André S., Surender Rajasekaran, Jeremy W. Prokop, et al.. (2021). Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome. American Journal of Medical Genetics Part A. 185(11). 3485–3493. 12 indexed citations

Lipson, Mark, Mary E. Prendergast, Isabelle Ribot, Carles Lalueza‐Fox, & David Reich. (2019). Ancient Human DNA from Shum Laka (Cameroon) in the Context of African Population History. 1 indexed citations

Lipson, Mark & David Reich. (2016). A working model of the deep relationships of diverse modern human genetic lineages outside of Africa. Molecular Biology and Evolution. 34(4). msw293–msw293. 38 indexed citations

Lipson, Mark, Po‐Ru Loh, Sriram Sankararaman, et al.. (2015). Calibrating the Human Mutation Rate via Ancestral Recombination Density in Diploid Genomes. PLoS Genetics. 11(11). e1005550–e1005550. 41 indexed citations

Meyer, Pablo, Thomas Cokelaer, Deepak Chandran, et al.. (2014). Network topology and parameter estimation: from experimental design methods to gene regulatory network kinetics using a community based approach. BMC Systems Biology. 8(1). 13–13. 44 indexed citations

Lipson, Mark, Po‐Ru Loh, Nick Patterson, et al.. (2014). Reconstructing Austronesian population history in Island Southeast Asia. Nature Communications. 5(1). 4689–4689. 117 indexed citations

Lipson, Mark, Po‐Ru Loh, A. Levin, et al.. (2013). Efficient Moment-Based Inference of Admixture Parameters and Sources of Gene Flow. Molecular Biology and Evolution. 30(8). 1788–1802. 75 indexed citations

Moorjani, Priya, Kumarasamy Thangaraj, Nick Patterson, et al.. (2013). Genetic Evidence for Recent Population Mixture in India. The American Journal of Human Genetics. 93(3). 422–438. 180 indexed citations

10.

Loh, Po‐Ru, Mark Lipson, Nick Patterson, et al.. (2012). Inference of Admixture Parameters in Human Populations Using Weighted Linkage Disequilibrium. arXiv (Cornell University). 2 indexed citations

11.

Arnold, Georgianne L., Denise Salazar, Julie Neidich, et al.. (2012). Outcome of infants diagnosed with 3-methyl-crotonyl-CoA-carboxylase deficiency by newborn screening. Molecular Genetics and Metabolism. 106(4). 439–441. 18 indexed citations

12.

Wiszniewska, Joanna, Mark Lipson, David R. Witt, et al.. (2011). Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysis. Journal of Human Genetics. 56(12). 834–839. 16 indexed citations

13.

Trefz, Friedrich K., Barbara K. Burton, Nicola Longo, et al.. (2009). Efficacy of Sapropterin Dihydrochloride in Increasing Phenylalanine Tolerance in Children with Phenylketonuria: A Phase III, Randomized, Double-Blind, Placebo-Controlled Study. The Journal of Pediatrics. 154(5). 700–707.e1. 156 indexed citations

14.

Dimmock, David, Carlo Dionisi‐Vici, Rosalba Carrozzo, et al.. (2008). Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase. Human Mutation. 29(2). 330–331. 123 indexed citations

15.

Lipson, Mark. (2005). Common neonatal syndromes. Seminars in Fetal and Neonatal Medicine. 10(3). 221–231. 4 indexed citations

16.

Lipson, Mark, et al.. (1999). Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiency. Prenatal Diagnosis. 19(4). 383–385. 7 indexed citations

17.

Paznekas, William A., Michael L. Cunningham, Timothy D. Howard, et al.. (1998). Genetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR Mutations. The American Journal of Human Genetics. 62(6). 1370–1380. 160 indexed citations

18.

Spritz, Richard A., Seung‐Taek Lee, Kazuyoshi Fukai, et al.. (1997). Novel mutations of theP gene in type II oculocutaneous albinism (OCA2). Human Mutation. 10(2). 175–177. 16 indexed citations

19.

Fujimoto, Atsuko, Judith Allanson, Carol A. Crowe, Mark Lipson, & Virginia P. Johnson. (1992). Natural history of mosaic trisomy 14 syndrome. American Journal of Medical Genetics. 44(2). 189–196. 37 indexed citations

20.

Fujimoto, Atsuko, Mark Lipson, Ronald V. Lacro, et al.. (1987). New autosomal dominant branchio‐oculo‐facial syndrome. American Journal of Medical Genetics. 27(4). 943–951. 56 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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