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Hire Dr. Anuj M.

United States

Tutor and editor specializing in (Molecular) Biology and (Molecular) Genetics

Profile Summary

As a Ph.D. in Molecular Medical Genetics (with two post-doctoral fellowships) and current contract tutor, I have experience and interests in research, teaching, and general scientific communication regarding general and molecular genetics, molecular biology, and, especially, the molecular pathology of inherited genetic diseases and cancers.

Subject Matter Expertise

• ☆ Animal Genetics
• ☆ Molecular Biology
• ☆ Genetics
• ☆ Phylogenetics
• ☆ Medical Genetics
• ☆ Molecular Pathology
• ☆ Rare Diseases

Services

• Writing
• Consulting
• Data & AI
• Product Development

Work Experience

Contract Tutor (in Biology)

WyzAnt Tutoring Services

February 2013 - Present

Freelance Editor

Cactus Communications Private Limited

May 2014 - November 2014

Postdoctoral Research Scholar / Research Investigator

University of Iowa Roy J and Lucille A Carver College of Medicine

July 2009 - July 2011

Postdoctoral Research Fellow

Cincinnati Children's Hospital Medical Center

February 2006 - December 2008

Education

Ph.D. (Molecular & Medical Genetics)

Oregon Health and Science University

September 1998 - June 2006

B.Sc. (Biology)

Brown University

September 1994 - May 1998

Certifications

• Certification details not provided.

Publications

JOURNAL ARTICLE

Anuj Mankad, Gabriel de la Garza, Jack Robert Schleiffarth, Martine Dunnwald, Jason L. Weirather, Gregory Bonde, Stephen Butcher, Tamer A. Mansour, Youssef A. Kousa, Cindy F. Fukazawa, et al.(2013). Interferon Regulatory Factor 6 Promotes Differentiation of the Periderm by Activating Expression of Grainyhead-Like 3 . Journal of Investigative Dermatology. 133. (1). p. 68--77. Elsevier {BV}

A. Mankad(2006). Natural gene therapy in monozygotic twins with Fanconi anemia . Blood. 107. (8). p. 3084--3090. American Society of Hematology

Anuj Mankad, Maria Pia Cosma, Stefano Pepe, Giancarlo Parenti, Carmine Settembre, Ida Annunziata, Richard Wade-Martins, Carmela Di Domenico, Paola Di Natale, Barbara Cox, et al.(2004). Molecular and functional analysis {ofSUMF}1 mutations in multiple sulfatase deficiency . Human Mutation. 23. (6). p. 576--581. Wiley-Blackwell

M. O'Connor(2001). Mutagenesis of the peptidyltransferase center of 23S {rRNA}: the invariant U2449 is dispensable . Nucleic Acids Research. 29. (3). p. 710--715. Oxford University Press ({OUP})