D. Boom

发表

A strategy for rapid and efficient DNA sequencing by mass spectrometry

C. Cantor, R. Cotter, Cassandra L. Smith, 1996, Nature Biotechnology.

Direct detection of synthetic and biologically generated double-stranded DNA by MALDI-TOF MS

H. Köster, A. Braun, D. Boom, 1997 .

Circulating cell free DNA testing: are some test failures informative?

G. Lambert-Messerlian, J. Haddow, G. Palomaki, 2015, Prenatal diagnosis.

Sequence Analysis of Nucleic Acids by Mass Spectrometry

H. Köster, D. Fu, D. Boom, 2000 .

Mass Spectrometric DNA Diagnostics

H. Köster, D. Boom, C. Jurinke, 1998 .

Comment on “Clinical application of massively parallel sequencing‐based prenatal non‐invasive fetal trisomy test for trisomies 21 and 18 in 11 105 pregnancies with mixed risk factors”

C. Cantor, C. Deciu, D. Boom, 2013, Prenatal diagnosis.

DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study

S. Nelson, W. Grody, J. Canick, 2011, Genetics in Medicine.

Response to Palomaki and Haddow

D. Grosu, M. Ehrich, D. Boom, 2016 .

Maternal plasma DNA testing for aneuploidy in pregnancies achieved by assisted reproductive technologies

G. Lambert-Messerlian, G. Palomaki, L. Wilkins-Haug, 2013, Genetics in Medicine.

MALDI-TOF MS: a platform technology for genetic discovery

M. Nelson, C. Cantor, R. Roth, 2004 .

MALDI-TOF mass spectrometry

Paul Oeth, D. Boom, P. Oeth, 2004, Molecular biotechnology.

Downregulation of RUNX3 and TES by hypermethylation in glioblastoma

D. Louis, C. Nutt, A. Deimling, 2007, Oncogene.

Oct4-Induced Pluripotency in Adult Neural Stem Cells

Marcos J. Araúzo-Bravo, David Ruau, Martin Zenke, 2009, Cell.

The C/EBPδ tumor suppressor is silenced by hypermethylation in acute myeloid leukemia

W. Hofmann, S. Koschmieder, W. Berdel, 2007 .

Chapter 3 Comparative Sequence Analysis by MALDI-TOF Mass Spectrometry – Utilizing the Known to Discover the New

F. Hillenkamp, M. Ehrich, D. Boom, 2007 .

Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts

John Tynan, Paul Oeth, Cosmin Deciu, 2015, Prenatal diagnosis.

Comparative genome sequencing of Escherichia coli allows observation of bacterial evolution on a laboratory timescale

Anu Raghunathan, Christiane Honisch, Bernhard Ø Palsson, 2006, Nature Genetics.

Maldi-Tof Ms: Applications in Genomics

C. Cantor, M. Ehrich, D. Boom, 2005 .

Single nucleotide polymorphism analyses by MALDI-TOF MS

C. Cantor, K. Abel, A. Braun, 2003 .

DNA sequencing of maternal plasma to identify Down syndrome and other trisomies in multiple gestations

Cosmin Deciu, J. Canick, G. Lambert-Messerlian, 2012, Prenatal diagnosis.

Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell‐free DNA from maternal plasma

W. Meschino, J. Canick, G. Palomaki, 2013, Prenatal diagnosis.

Application of risk score analysis to low‐coverage whole genome sequencing data for the noninvasive detection of trisomy 21, trisomy 18, and trisomy 13

T. Burcham, G. Hannum, M. Ehrich, 2016, Prenatal diagnosis.

MALDI‐MS of Nucleic Acids and Practical Implementations in Genomics and Genetics

D. Boom, S. Berkenkamp, 2007 .

Multiplexed Analysis of Circulating Cell-Free Fetal Nucleic Acids for Noninvasive Prenatal Diagnostic RHD Testing

M. Ehrich, D. Boom, P. Oeth, 2011 .

Small Cell Lung Cancer − Cytosine Methylation Profiles as a Molecular Marker in Non

M. Nelson, C. Cantor, T. Liloglou, 2006 .

myeloid leukemia tumor suppressor is silenced by hypermethylation in acute Δ The C/EBP

W. Hofmann, W. Berdel, C. Müller-Tidow, 2013 .

Automated genotyping using the DNA MassArray technology.

C. Cantor, D. van den Boom, H. Köster, 2001, Methods in molecular biology.

Differential Sequencing by Mass Spectrometry

D. Boom, C. Jurinke, C. Honisch, 2004 .

Analysis of Nucleic Acids by Mass Spectrometry

F. Hillenkamp, D. Boom, 2005 .