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Genetics

D-Index
88
Citations
31337
World Ranking
1159
National Ranking
556

Medicine

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89
Citations
31841
World Ranking
12606
National Ranking
6446

Overview

Matthew L. Warman is affiliated with Boston Children's Hospital in the United States. Their research spans multiple areas within biochemistry, genetics, molecular biology, and medicine, contributing significantly to the understanding of skeletal biology and related disorders.

The scientist's main fields of study include:

  • Biochemistry, Genetics and Molecular Biology
  • Medicine

Within these fields, their subfields of focus are:

  • Molecular Biology
  • Genetics
  • Orthopedics and Sports Medicine
  • Immunology
  • Oncology

The primary topics covered in their work involve:

  • Connective tissue disorders research
  • Wnt/β-catenin signaling in development and cancer
  • Vascular Anomalies and Treatments
  • Bone health and osteoporosis research
  • Osteoarthritis Treatment and Mechanisms
  • Immunodeficiency and Autoimmune Disorders
  • Bone health and treatments

Among the recent scholarly publications of Matthew L. Warman are:

  • Nosology of genetic skeletal disorders: 2023 revision, 2023, American Journal of Medical Genetics Part A
  • An osteocalcin-deficient mouse strain without endocrine abnormalities, 2020, PLoS Genetics
  • Single-Cell RNA Sequencing of Calvarial and Long-Bone Endocortical Cells, 2020, Journal of Bone and Mineral Research
  • Unique and non-redundant function of csf1r paralogues in regulation and evolution of post-embryonic development of the zebrafish, 2020, Development
  • Sensitive detection of Cre-mediated recombination using droplet digital PCR reveals Tg(BGLAP-Cre) and Tg(DMP1-Cre) are active in multiple non-skeletal tissues, 2020, Bone

Matthew L. Warman frequently publishes in journals such as:

  • Bone
  • PLoS Genetics
  • Journal of Bone and Mineral Research
  • Development
  • PLoS ONE

Collaborations have been established with several researchers who appear frequently alongside Warman in publications. These co-authors include:

  • Alexander G. Robling
  • Ugur M. Ayturk
  • Steven Hann
  • Kyung-Eun Lim
  • Bart O. Williams

Best Publications

  • LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development

    Y. Q. Gong;R. B. Slee;N. Fukai;G. Rawadi

  • Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT)

    G.E. Truett;P. Heeger;R.L. Mynatt;A.A. Truett

  • Vascular Dysmorphogenesis Caused by an Activating Mutation in the Receptor Tyrosine Kinase TIE2

    Miikka Vikkula;Laurence M Boon;Kermit L.Carraway;Jennifer T Calvert

  • A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

    Ethylin Wang Jabs;Ulrich Müller;Xiang Li;Liang Ma

  • Nosology and classification of genetic skeletal disorders : 2010 revision

    Matthew L. Warman;Valerie Cormier-Daire;Christine Hall;Deborah Krakow;Deborah Krakow

  • The secreted glycoprotein lubricin protects cartilage surfaces and inhibits synovial cell overgrowth

    David K. Rhee;Jose Marcelino;MacArthur Baker;Yaoqin Gong

  • Six Novel Missense Mutations in the LDL Receptor-Related Protein 5 (LRP5) Gene in Different Conditions with an Increased Bone Density

    Liesbeth Van Wesenbeeck;Erna Cleiren;Jeppe Gram;Rodney K. Beals

  • Nosology and classification of genetic skeletal disorders: 2015 revision

    Luisa Bonafe;Valerie Cormier-Daire;Christine Hall;Ralph Lachman

  • Lrp5-independent activation of Wnt signaling by lithium chloride increases bone formation and bone mass in mice.

    Philippe Clément-Lacroix;Minrong Ai;Frederic Morvan;Sergio Roman-Roman

  • Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome

    Kyle C. Kurek;Valerie L. Luks;Ugur M. Ayturk;Ugur M. Ayturk;Ahmad I. Alomari

  • Lymphatic and Other Vascular Malformative/Overgrowth Disorders Are Caused by Somatic Mutations in PIK3CA

    Valerie L. Luks;Nolan Kamitaki;Matthew P. Vivero;Wibke Uller

  • Nosology and classification of genetic skeletal disorders: 2019 revision.

    Geert R Mortier;Daniel H Cohn;Valerie Cormier-Daire;Christine Hall

  • Lrp5 functions in bone to regulate bone mass

    Yajun Cui;Paul J Niziolek;Paul J Niziolek;Bryan T MacDonald;Cassandra R Zylstra

  • The Wnt co-receptor LRP5 is essential for skeletal mechanotransduction but not for the anabolic bone response to parathyroid hormone treatment.

    Kimihiko Sawakami;Alexander G. Robling;Minrong Ai;Nathaniel D. Pitner

  • Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

    Miikka Vikkula;Edwin C.M Madman;Vincent C.H Lui;Natalia I Zhidkova

  • Improving the DNA specificity and applicability of base editing through protein engineering and protein delivery.

    Holly A. Rees;Holly A. Rees;Holly A. Rees;Alexis C. Komor;Alexis C. Komor;Alexis C. Komor;Wei-Hsi Yeh;Joana Caetano-Lopes;Joana Caetano-Lopes

  • Decreased BMD and limb deformities in mice carrying mutations in both Lrp5 and Lrp6.

    Sheri L Holmen;Troy A Giambernardi;Cassandra R Zylstra;Bree D Buckner-Berghuis

  • A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesis

    Y Li;D.A Lacerda;M.L Warman;D.R Beier

  • Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux

    Cynthia F. Bartels;Hülya Bükülmez;Hülya Bükülmez;Pius Padayatti;David K. Rhee

  • Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis.

    Yaoqin Gong;Deborah Krakow;Deborah Krakow;Jose Marcelino;Douglas Wilkin

Frequent Co-Authors

John B. Mulliken
John B. Mulliken Boston Children's Hospital
Björn Olsen
Björn Olsen Harvard University
Stefan Mundlos
Stefan Mundlos Max Planck Society
Daniel H. Cohn
Daniel H. Cohn University of California, Los Angeles
Bart O. Williams
Bart O. Williams Van Andel Institute
David L. Rimoin
David L. Rimoin Cedars-Sinai Medical Center
Miikka Vikkula
Miikka Vikkula Université Catholique de Louvain
Yaoqin Gong
Yaoqin Gong Shandong University
Deborah Krakow
Deborah Krakow University of California, Los Angeles
Harry P. W. Kozakewich
Harry P. W. Kozakewich Boston Children's Hospital

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