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Genetics

D-Index
88
Citations
29426
World Ranking
1168
National Ranking
562

Molecular Biology

D-Index
88
Citations
29426
World Ranking
780
National Ranking
414

Overview

Richard L. Maas is affiliated with Brigham and Women's Hospital in the United States. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, with significant contributions also in Medicine. The scientist's work engages extensively with subfields such as Molecular Biology, Genetics, Cell Biology, Epidemiology, and Physiology.

The primary research topics covered by Maas include:

  • Cleft Lip and Palate Research
  • Craniofacial Disorders and Treatments
  • Cellular transport and secretion
  • Metabolism and Genetic Disorders
  • Cancer-related gene regulation
  • Autophagy in Disease and Therapy
  • Genomics and Rare Diseases

Maas's recent published papers demonstrate ongoing activity in genetic medicine and developmental biology. Selected publications include:

  • FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research, 2020, Development
  • An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids, 2020, Genetics in Medicine
  • Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science, 2020, Genetics in Medicine
  • SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia, 2023, Brain
  • Imaging Mass Spectrometry Reveals Tumor Metabolic Heterogeneity, 2020, iScience

Among frequent collaborators are Elizabeth L. Fieg, Rebecca C. Spillmann, Joel B. Krier, Michael F. Wangler, and Allyn McConkie-Rosell. The number of coauthored publications range from 9 to 11 with these colleagues, indicating established research partnerships.

The venues where Maas has commonly published include Genetics in Medicine, bioRxiv (Cold Spring Harbor Laboratory), EMBO Molecular Medicine, Proceedings of the National Academy of Sciences, and Blood. Genetics in Medicine is the most frequent, with five publications attributed to Maas.

Best Publications

  • Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

    Ichiro Satokata;Richard Maas

  • Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation.

    Ichiro Satokata;Liang Ma;Hayato Ohshima;Marianna Bei

  • Sonic hedgehog regulates growth and morphogenesis of the tooth

    Hélène R. Dassule;Paula Lewis;Marianna Bei;Richard Maas

  • PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects

    Thomas M Glaser;L. Jepeal;J. G. Edwards;S. R. Young

  • Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene.

    Tom Glaser;David S. Walton;Richard L. Maas

  • Endogenous biosynthesis of prostacyclin and thromboxane and platelet function during chronic administration of aspirin in man.

    G A FitzGerald;J A Oates;J Hawiger;R L Maas

  • Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia.

    Xu Px;Adams J;Peters H;Brown Mc

  • Eya protein phosphatase activity regulates Six1–Dach–Eya transcriptional effects in mammalian organogenesis

    Xue Li;Kenneth A. Oghi;Jie Zhang;Anna Krones

  • Sexually dimorphic sterility phenotypes in Hoxa10-deficient mice.

    Ichiro Satokata;Gail Benson;Richard Maas

  • Mechanisms of reduced fertility in Hoxa-10 mutant mice: uterine homeosis and loss of maternal Hoxa-10 expression

    Gail V. Benson;Hyunjung Lim;B. C. Paria;Ichiro Satokata

  • Crystal structure of the human Pax6 paired domain-DNA complex reveals specific roles for the linker region and carboxy-terminal subdomain in DNA binding.

    H. E. Xu;M. A. Rould;Wenqing Xu;J. A. Epstein

  • Msx1 controls inductive signaling in mammalian tooth morphogenesis

    YiPing Chen;Marianna Bei;Ian Woo;Ichiro Satokata

  • FGFs and BMP4 induce both Msx1-independent and Msx1-dependent signaling pathways in early tooth development

    Marianna Bei;Richard Maas

  • Quantifying cell-generated mechanical forces within living embryonic tissues

    Otger Campàs;Tadanori Mammoto;Sean Hasso;Ralph A Sperling

  • Pax3 modulates expression of the c-Met receptor during limb muscle development.

    Jonathan A. Epstein;David N. Shapiro;Jane Cheng;Paula Y. P. Lam

  • Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing.

    Jonathan A. Epstein;Thomas M Glaser;Jiexing Cai;Lisa Jepeal

  • Identification of a Pax paired domain recognition sequence and evidence for DNA-dependent conformational changes.

    Jonathan Epstein;Jiexing Cai;Thomas M Glaser;Lisa Jepeal

  • BMP7 acts in murine lens placode development.

    Stefan Wawersik;Patricia Purcell;Michael Rauchman;Andrew T. Dudley

  • Hoxa-10 regulates uterine stromal cell responsiveness to progesterone during implantation and decidualization in the mouse.

    Hyunjung Lim;Liang Ma;Wen-ge Ma;Richard L. Maas

  • Mouse Eya homologues of the Drosophila eyes absent gene require Pax6 for expression in lens and nasal placode

    Pin-Xian Xu;Ian Woo;Helen Her;David R. Beier

Frequent Co-Authors

Cynthia C. Morton
Cynthia C. Morton Brigham and Women's Hospital
Christopher A. Walsh
Christopher A. Walsh Howard Hughes Medical Institute
Joseph Loscalzo
Joseph Loscalzo Harvard Medical School
Calum A. MacRae
Calum A. MacRae Brigham and Women's Hospital
David A. Sweetser
David A. Sweetser Harvard University
Michael F. Wangler
Michael F. Wangler Baylor College of Medicine
Seema R. Lalani
Seema R. Lalani Baylor College of Medicine
Janet S. Sinsheimer
Janet S. Sinsheimer University of California, Los Angeles
Jill A. Rosenfeld
Jill A. Rosenfeld Baylor College of Medicine
Hane Lee
Hane Lee University of California, Los Angeles

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