Works by LIPSON, MARK

Results: 23

Revisiting ancient DNA insights into the human history of the Pacific Islands.

Published in:

2019

By:

SPRIGGS, MATTHEW;
VALENTIN, FREDERIQUE;
BEDFORD, STUART;
PINHASI, RON;
SKOGLUND, PONTUS;
REICH, DAVID;
LIPSON, MARK

Publication type:

Letter to the Editor

Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysis.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 12, p. 834, doi. 10.1038/jhg.2011.112

By:

Douglas, Ganka V;
Wiszniewska, Joanna;
Lipson, Mark H;
Witt, David R;
McDowell, Taryn;
Sifry-Platt, Mara;
Hirano, Michio;
Craigen, William J;
Wong, Lee-Jun C

Publication type:

Article

South-to-north migration preceded the advent of intensive farming in the Maya region.

Published in:

Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29158-y

By:

Kennett, Douglas J.;
Lipson, Mark;
Prufer, Keith M.;
Mora-Marín, David;
George, Richard J.;
Rohland, Nadin;
Robinson, Mark;
Trask, Willa R.;
Edgar, Heather H. J.;
Hill, Ethan C.;
Ray, Erin E.;
Lynch, Paige;
Moes, Emily;
O'Donnell, Lexi;
Harper, Thomas K.;
Kate, Emily J.;
Ramos, Josue;
Morris, John;
Gutierrez, Said M.;
Ryan, Timothy M.

Publication type:

Article

Social stratification without genetic differentiation at the site of Kulubnarti in Christian Period Nubia.

Published in:

Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-27356-8

By:

Sirak, Kendra A.;
Fernandes, Daniel M.;
Lipson, Mark;
Mallick, Swapan;
Mah, Matthew;
Olalde, Iñigo;
Ringbauer, Harald;
Rohland, Nadin;
Hadden, Carla S.;
Harney, Éadaoin;
Adamski, Nicole;
Bernardos, Rebecca;
Broomandkhoshbacht, Nasreen;
Callan, Kimberly;
Ferry, Matthew;
Lawson, Ann Marie;
Michel, Megan;
Oppenheimer, Jonas;
Stewardson, Kristin;
Zalzala, Fatma

Publication type:

Article

Rethinking the Vision for Environmental Research in US Agriculture.

Published in:

BioScience, 2004, v. 54, n. 1, p. 61, doi. 10.1641/0006-3568(2004)054[0061:RTVFER]2.0.CO;2

By:

Robertson, G. Philip;
Broome, Janet C.;
Chornesky, Elizabeth A.;
Frankenberger, Jane R.;
Johnson, Paul;
Lipson, Mark;
Miranowski, John A.;
Owens, Elizabeth D.;
Pimentel, David;
Thrupp, Lori Ann

Publication type:

Article

Calibrating the Human Mutation Rate via Ancestral Recombination Density in Diploid Genomes.

Published in:

PLoS Genetics, 2015, v. 11, n. 10, p. 1, doi. 10.1371/journal.pgen.1005550

By:

Lipson, Mark;
Loh, Po-Ru;
Sankararaman, Sriram;
Patterson, Nick;
Berger, Bonnie;
Reich, David

Publication type:

Article

A Working Model of the Deep Relationships of Diverse Modern Human Genetic Lineages Outside of Africa.

Published in:

Molecular Biology & Evolution, 2017, v. 34, n. 4, p. 889, doi. 10.1093/molbev/msw293

By:

Lipson, Mark;
Reich, David

Publication type:

Article

Efficient Moment-Based Inference of Admixture Parameters and Sources of Gene Flow.

Published in:

Molecular Biology & Evolution, 2013, v. 30, n. 8, p. 1788, doi. 10.1093/molbev/mst099

By:

Lipson, Mark;
Loh, Po-Ru;
Levin, Alex;
Reich, David;
Patterson, Nick;
Berger, Bonnie

Publication type:

Article

Interactions between earliest Linearbandkeramik farmers and central European hunter gatherers at the dawn of European Neolithization.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-56029-2

By:

Nikitin, Alexey G.;
Stadler, Peter;
Kotova, Nadezhda;
Teschler-Nicola, Maria;
Price, T. Douglas;
Hoover, Jessica;
Kennett, Douglas J.;
Lazaridis, Iosif;
Rohland, Nadin;
Lipson, Mark;
Reich, David

Publication type:

Article

Pharmacokinetics of Sapropterin in Patients with Phenylketonuria.

Published in:

Clinical Pharmacokinetics, 2008, v. 47, n. 12, p. 817, doi. 10.2165/0003088-200847120-00006

By:

Feillet, François;
Clarke, Lorne;
Meli, Concetta;
Lipson, Mark;
Morris, Andrew A.;
Harmatz, Paul;
Mouldi, Diane R.;
Green, Bruce;
Dorenbaum, Alex;
Giovannim, Marcello;
Foehr, Erik

Publication type:

Article

No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.

Published in:

Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0271-4

By:

Schlögel, Matthieu J.;
Mendola, Antonella;
Fastré, Elodie;
Vasudevan, Pradeep;
Devriendt, Koen;
de Ravel, Thomy J. L.;
Van Esch, Hilde;
Casteels, Ingele;
Arroyo Carrera, Ignacio;
Cristofoli, Francesca;
Fieggen, Karen;
Jones, Katheryn;
Lipson, Mark;
Balikova, Irina;
Singer, Ami;
Soller, Maria;
Villanueva, María Mercedes;
Revencu, Nicole;
Boon, Laurence M.;
Brouillard, Pascal

Publication type:

Article

No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.

Published in:

Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 52, doi. 10.1186/s13023-015-0271-4

By:

Schlögel, Matthieu J;
Mendola, Antonella;
Fastré, Elodie;
Vasudevan, Pradeep;
Devriendt, Koen;
de Ravel, Thomy JL;
Van Esch, Hilde;
Casteels, Ingele;
Carrera, Ignacio Arroyo;
Cristofoli, Francesca;
Fieggen, Karen;
Jones, Katheryn;
Lipson, Mark;
Balikova, Irina;
Singer, Ami;
Soller, Maria;
Villanueva, María Mercedes;
Revencu, Nicole;
Boon, Laurence M;
Brouillard, Pascal

Publication type:

Article

No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.

Published in:

2015

By:

Schlögel, Matthieu J;
Mendola, Antonella;
Fastré, Elodie;
Vasudevan, Pradeep;
Devriendt, Koen;
de Ravel, Thomy Jl;
Van Esch, Hilde;
Casteels, Ingele;
Arroyo Carrera, Ignacio;
Cristofoli, Francesca;
Fieggen, Karen;
Jones, Katheryn;
Lipson, Mark;
Balikova, Irina;
Singer, Ami;
Soller, Maria;
Mercedes Villanueva, María;
Revencu, Nicole;
Boon, Laurence M;
Brouillard, Pascal

Publication type:

journal article

Network topology and parameter estimation: from experimental design methods to gene regulatory network kinetics using a community based approach.

Published in:

BMC Systems Biology, 2014, v. 8, n. 1, p. 1, doi. 10.1186/1752-0509-8-13

By:

Meyer, Pablo;
Cokelaer, Thomas;
Chandran, Deepak;
Kyung Hyuk Kim;
Po-Ru Loh;
Tucker, George;
Lipson, Mark;
Berger, Bonnie;
Kreutz, Clemens;
Raue, Andreas;
Steiert, Bernhard;
Timmer, Jens;
Bilal, Erhan;
Sauro, Herbert M.;
Stolovitzky, Gustavo;
Saez-Rodriguez, Julio

Publication type:

Article

Novel mutations of the P gene in type II oculocutaneous albinism (OCA2).

Published in:

Human Mutation, 1997, v. 10, n. 2, p. 175, doi. 10.1002/(SICI)1098-1004(1997)10:2<175::AID-HUMU12>3.0.CO;2-X

By:

Spritz, Richard A.;
Lee, Seung-Taek;
Fukai, Kazuyoshi;
Brondum-Nielsen, Karen;
Chitayat, David;
Lipson, Mark H.;
Musarella, Maria A.;
Rosenmann, Ada;
Weleber, Richard G.

Publication type:

Article

Reconstructing Austronesian population history in Island Southeast Asia.

Published in:

Nature Communications, 2014, v. 5, n. 8, p. 4689, doi. 10.1038/ncomms5689

By:

Lipson, Mark;
Loh, Po-Ru;
Patterson, Nick;
Moorjani, Priya;
Ko, Ying-Chin;
Stoneking, Mark;
Berger, Bonnie;
Reich, David

Publication type:

Article

Applying f<sub>4</sub>‐statistics and admixture graphs: Theory and examples.

Published in:

Molecular Ecology Resources, 2020, v. 20, n. 6, p. 1658, doi. 10.1111/1755-0998.13230

By:

Lipson, Mark

Publication type:

Article

Ruvalcaba-Myhre-Smith Syndrome.

Published in:

Pediatric Dermatology, 1988, v. 5, n. 1, p. 28, doi. 10.1111/j.1525-1470.1988.tb00880.x

By:

Gretzula, Joseph C.;
Helvia, Oscar;
Schachner, Lawrence S.;
DiLiberti, John H.;
Ruvalcaba, R. H. A.;
Schimschock, James R.;
Welber, Richard G.;
Halal, Fahed;
Lipson, Mark H.;
Blumberg, Bruce;
Webeer, Paul J.

Publication type:

Article

Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2021, v. 185, n. 11, p. 3485, doi. 10.1002/ajmg.a.62473

By:

VanSickle, Elizabeth A.;
Michael, Julianne;
Bachmann, André S.;
Rajasekaran, Surender;
Prokop, Jeremy W.;
Kuzniecky, Ruben;
Hofstede, Floris C.;
Steindl, Katharina;
Rauch, Anita;
Lipson, Mark H.;
Bupp, Caleb P.

Publication type:

Article

Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiency.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 4, p. 383, doi. 10.1002/(SICI)1097-0223(199904)19:4<383::AID-PD544>3.0.CO;2-S

By:

Brookhyser, Karen M.;
Lipson, Mark H.;
Moser, Ann B.;
Moser, Hugo W.;
Lachman, Ralph S.;
Rimoin, David L.

Publication type:

Article

Reconstructing Roma History from Genome-Wide Data.

Published in:

PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058633

By:

Moorjani, Priya;
Patterson, Nick;
Loh, Po-Ru;
Lipson, Mark;
Kisfali, Péter;
Melegh, Bela I.;
Bonin, Michael;
Kádaši, Ľudevít;
Rieß, Olaf;
Berger, Bonnie;
Reich, David;
Melegh, Béla

Publication type:

Article

Practice and attitudes regarding double gloving among staff surgeons and surgical trainees.

Published in:

2018

By:

Lipson, Mark E.;
Deardon, Rob;
Switzer, Noah J.;
de Gara, Chris;
Ball, Chad G.;
Grondin, Sean C.

Publication type:

journal article

Inferring Admixture Histories of Human Populations Using Linkage Disequilibrium.

Published in:

Genetics, 2013, v. 193, n. 4, p. 1233, doi. 10.1534/genetics.112.147330

By:

Loh, Po-Ru;
Lipson, Mark;
Patterson, Nick;
Moorjani, Priya;
Pickrell, Joseph K.;
Reich, David;
Berger, Bonnie

Publication type:

Article