Mark Lipson

13.8k citations

62 papers · 2.4k indexed · 1 hit paper · h-index 26

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Genetics top 1%
- Forensic and Genetic Research
- Genetic diversity and population structure
- Craniofacial Disorders and Treatments
- Genetic Associations and Epidemiology

Papers in ⓘ

Clinical Biochemistry 13
- Metabolism and Genetic Disorders 13
Genetics 30
- Forensic and Genetic Research 15
- Connective tissue disorders research 5

Co-authors: David Reich (16 shared papers)Bonnie Berger (12 shared papers)Po‐Ru Loh (12 shared papers)Priya Moorjani (6 shared papers)Nick Patterson (7 shared papers)Joseph K. Pickrell (5 shared papers)Nick Patterson (4 shared papers)Mark Stoneking (4 shared papers)
Journals: The Journal of Pediatrics (3 papers)The American Journal of Human Genetics (3 papers)Molecular Genetics and Metabolism (3 papers)Human Mutation (3 papers)Radiology (2 papers)
Partner nations: United States Canada Germany

In The Last Decade

Mark Lipson

61 papers receiving 2.3k citations

Hit Papers

align trajectories log scale

Inferring Admixture Histories of Human Populations Using Linkage Disequilibrium 2013 · 272 citations

Peers

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-authors

The 25 scholars most cited alongside Mark Lipson, 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 Mark Lipson Line = papers co-authored together Mark Lipson 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 62 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Inferring Admixture Histories of Human Populations Using Linkage Disequilibrium Genetics ·Po‐Ru Loh, Mark Lipson, Nick Patterson, Priya Moorjani, Joseph K. Pickrell, David Reich, Bonnie Berger Hit paper breakdown →	2013	272
2	Genetic Evidence for Recent Population Mixture in India The American Journal of Human Genetics ·Priya Moorjani, Kumarasamy Thangaraj, Nick Patterson, Mark Lipson, Po‐Ru Loh, Periyasamy Govindaraj, Bonnie Berger, David Reich, Lalji Singh	2013	180
3	Genetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR Mutations The American Journal of Human Genetics ·William A. Paznekas, Michael L. Cunningham, Timothy D. Howard, Bruce R. Korf, Mark Lipson, Art Grix, Murray Feingold, Rosalie Goldberg, Zvi Borochowitz, Kirk Aleck, John B. Mulliken, Mingfei Yin, Ethylin Wang Jabs	1998	160
4	Ancient west Eurasian ancestry in southern and eastern Africa Proceedings of the National Academy of Sciences ·Joseph K. Pickrell, Nick Patterson, Po‐Ru Loh, Mark Lipson, Bonnie Berger, Mark Stoneking, Brigitte Pakendorf, David Reich	2014	160
5	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 ·Friedrich K. Trefz, Barbara K. Burton, Nicola Longo, Mercedes Martinez-Pardo Casanova, Daniel Gruskin, Alex Dorenbaum, Emil Kakkis, Eric Crombez, Dorothy K. Grange, Paul Harmatz, Mark Lipson, Andrzej Milanowski, Linda M. Randolph, Jerry Vockley, Chester B. Whitley, Jon A. Wolff, Judith D. Bebchuk, Heidi Christ‐Schmidt, Julia B. Hennermann	2009	156
6	Diverse Mutations in the Gene for Cartilage Oligomeric Matrix Protein in the Pseudoachondroplasia–Multiple Epiphyseal Dysplasia Disease Spectrum The American Journal of Human Genetics ·Michael D. Briggs, Geert Mortier, William G. Cole, Lily King, Steven S. Golik, Jacky Bonaventure, Lieve Nuytinck, Anne De Paepe, Jules G. Leroy, Leslie G. Biesecker, Mark Lipson, William R. Wilcox, Ralph S. Lachman, David L. Rimoin, Robert G. Knowlton, Daniel H. Cohn	1998	136
7	Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase Human Mutation ·David Dimmock, Q. Zhang, Carlo Dionisi‐Vici, Rosalba Carrozzo, Joseph T.C. Shieh, L-Y Tang, Cavatina K. Truong, Eric Schmitt, Mara Sifry-Platt, S. Lucioli, Filippo M. Santorelli, (unknown), Maria Angeles Rodríguez, Klaas J. Wierenga, Gregory M. Enns, Nicola Longo, Mark Lipson, Hilary Vallance, W. J. Craigen, Fernando Scaglia, L-J. C. Wong	2008	123
8	Reconstructing Austronesian population history in Island Southeast Asia Nature Communications ·Mark Lipson, Po‐Ru Loh, Nick Patterson, Priya Moorjani, Ying‐Chin Ko, Mark Stoneking, Bonnie Berger, David Reich	2014	117
9	Efficient Moment-Based Inference of Admixture Parameters and Sources of Gene Flow Molecular Biology and Evolution ·Mark Lipson, Po‐Ru Loh, A. Levin, David Reich, Nick Patterson, Bonnie Berger	2013	75
10	New autosomal dominant branchio‐oculo‐facial syndrome American Journal of Medical Genetics ·Atsuko Fujimoto, Mark Lipson, Ronald V. Lacro, Nancy W. Shinno, William D. Boelter, Kenneth L. Jones, Miriam G. Wilson, John M. Opitz, James F. Reynolds	1987	56
11	Reconstructing Roma History from Genome-Wide Data PLoS ONE ·Priya Moorjani, Nick Patterson, Po‐Ru Loh, Mark Lipson, Péter Kisfali, Béla Melegh, Michael Bonin, Ľudevít Kádaši, Olaf Rieß, Bonnie Berger, David Reich	2013	46
12	Maple syrup urine disease: Further evidence that newborn screening may fail to identify variant forms Molecular Genetics and Metabolism ·R.L. Puckett, Fred Lorey, Piero Rinaldo, Mark Lipson, Dietrich Matern, Mary Sowa, Stuart S. Levine, Richard Chang, R. Y. Wang, José E. Abdenur	2009	45
13	Network topology and parameter estimation: from experimental design methods to gene regulatory network kinetics using a community based approach BMC Systems Biology ·Pablo Meyer, Thomas Cokelaer, Deepak Chandran, Kyung Kim, Po‐Ru Loh, George Tucker, Mark Lipson, Bonnie Berger, Clemens Kreutz, Andreas Raue, Bernhard Steiert, Jens Timmer, Erhan Bilal, Herbert M. Sauro, Gustavo Stolovitzky, Julio Sáez-Rodríguez	2014	44
14	Calibrating the Human Mutation Rate via Ancestral Recombination Density in Diploid Genomes PLoS Genetics ·Mark Lipson, Po‐Ru Loh, Sriram Sankararaman, Nick Patterson, Bonnie Berger, David Reich	2015	41
15	Affinity of Cystathionine β-Synthase for Pyridoxal 5′-Phosphate in Cultured Cells Journal of Clinical Investigation ·Mark Lipson, Jan P. Kraus, León E. Rosenberg	1980	40
16	A working model of the deep relationships of diverse modern human genetic lineages outside of Africa Molecular Biology and Evolution ·Mark Lipson, David Reich	2016	38
17	Natural history of mosaic trisomy 14 syndrome American Journal of Medical Genetics ·Atsuko Fujimoto, Judith Allanson, Carol A. Crowe, Mark Lipson, Virginia P. Johnson	1992	37
18	Ultrasonographic Evaluation of Juxtadiaphragmatic Masses in Children Radiology ·Hooshang Kangarloo, Richard Sukov, W. Frederick Sample, Mark Lipson, Lorraine Smith	1977	34
19	Pharmacokinetics of Sapropterin in Patients with Phenylketonuria Clinical Pharmacokinetics ·François Feillet, L. Clarke, Concetta Meli, Mark Lipson, Andrew A. M. Morris, Paul Harmatz, Diane R. Mould, Bruce Green, Alex Dorenbaum, Marcello Giovannini, Erik D. Foehr	2008	33
20	Clinical and Biochemical Variation and Family Studies in the Multiple Acyl-CoA Dehydrogenation Disorders Pediatric Research ·William J. Rhead, Jon A. Wolff, Mark Lipson, Peggy Falace, Nirmala S. Desai, Kathie Fritchman, Anne Moon, Lawrence Sweetman	1987	33

About Mark Lipson

Mark Lipson is a scholar working on Clinical Biochemistry, Genetics, Archeology, Paleontology and Biochemistry, having authored 62 papers that have together received 2.4k indexed citations. Recurring topics across this work include Forensic and Genetic Research (15 papers), Metabolism and Genetic Disorders (13 papers), Forensic Anthropology and Bioarchaeology Studies (7 papers), Mitochondrial Function and Pathology (6 papers), Biochemical and Molecular Research (5 papers), Connective tissue disorders research (5 papers), Archaeology and ancient environmental studies (4 papers) and Pleistocene-Era Hominins and Archaeology (4 papers). The work is most often cited by research in Clinical Biochemistry (475 citations), Genetics (1.2k citations), Archeology (216 citations), Paleontology (111 citations) and Rheumatology (203 citations). Mark Lipson has collaborated with scholars based in United States, Canada and Germany. Frequent 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. Their work appears in journals such as The Journal of Pediatrics, The American Journal of Human Genetics, Molecular Genetics and Metabolism, Human Mutation and Radiology.

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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