Mathias Ehrich

8.2k citations

61 papers · 6.2k indexed · 5 hit papers · h-index 36

Impact in

Pediatrics, Perinatology and Child Health top 0.1%
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Cancer Research top 2%
- Cancer Genomics and Diagnostics

Papers in

Pediatrics, Perinatology and Child Health 30
- Prenatal Screening and Diagnostics 30
- Fetal and Pediatric Neurological Disorders 15
Cancer Research 16
- Cancer Genomics and Diagnostics 11

Co-authors: Dirk van den Boom Cosmin Deciu Allan T. Bombard Charles R. Cantor Glenn E. Palomaki Jacob A. Canick Edward M. Kloza Geralyn Lambert‐Messerlian
Journals: Clinical Chemistry (6 papers)American Journal of Obstetrics and Gynecology (5 papers)Prenatal Diagnosis (5 papers)Genetics in Medicine (4 papers)Oncogene (3 papers)
Partner nations: United States Germany United Kingdom

In The Last Decade

Mathias Ehrich

61 papers receiving 6.0k citations

Hit Papers

5 papers align trajectories log scale

DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study 2012 · 392 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2012 Genetics in Medicine
2011 Genetics in Medicine
2011 American Journal of Obstetrics and Gynecology
2009 Cell
2005 Proceedings of the National Academy of Sciences

Peers

Countries citing papers authored by Mathias Ehrich

Since Specialization

Citations

This map shows the geographic impact of Mathias Ehrich's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mathias Ehrich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mathias Ehrich more than expected).

Fields of papers citing papers by Mathias Ehrich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mathias Ehrich. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mathias Ehrich. The network helps show where Mathias Ehrich may publish in the future.

Co-authors

The 25 scholars most cited alongside Mathias Ehrich, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mathias Ehrich Line = papers co-authored together Mathias Ehrich links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Genome-Wide Sequencing of Cell-Free DNA Identifies Copy-Number Alterations That Can Be Used for Monitoring Response to Immunotherapy in Cancer Patients Molecular Cancer Therapeutics ·Taylor J. Jensen, Aaron M. Goodman, Shumei Kato, Christopher K. Ellison, Gregory A. Daniels, Lisa Kim, Ronaldo Toma, Erin McCarthy, Amin R. Mazloom, Graham McLennan, Daniel S. Grosu, Mathias Ehrich, Razelle Kurzrock	2018	67
2	Ultrasensitive Detection of Multiplexed Somatic Mutations Using MALDI-TOF Mass Spectrometry Journal of Molecular Diagnostics ·Kevin Venus, Aleksey Nakorchevsky, Beulah Divya Kannan, ○ Masahikoyasuda, Mathias Ehrich, T.G. WOOD, James Sherwood, Anders O.H. Nygren	2015	68
3	Whole genome bisulfite sequencing of cell-free DNA and its cellular contributors uncovers placenta hypomethylated domains Genome Biology ·Taylor J. Jensen, Sung K. Kim, Zhanyang Zhu, А. В. Андроник, Claudia Gebhard, Tim Lu, Cosmin Deciu, Dirk van den Boom, Mathias Ehrich	2015	54
4	Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA American Journal of Obstetrics and Gynecology ·Richard P. Porreco, Thomas J. Garite, Kimberly Maurel, Arjun Singh Bisht, Mathias Ehrich, Dirk van den Boom, Cosmin Deciu, Allan T. Bombard	2014	142
5	Optimizing blood collection, transport and storage conditions for cell free DNA increases access to prenatal testing Clinical Biochemistry ·David T. Wong, Cüneyt Akçatepe, Vach Angkachatchai, Reinhold Mueller, Grace DeSantis, Dirk van den Boom, Mathias Ehrich	2013	108
6	Stemness of the Organ of Corti Relates to the Epigenetic Status of Sox2 Enhancers PLoS ONE ·Derlis N. Britez, Friedrich U. Mathiak, Henning Gohlke, Mathias Ehrich, Marcus Müller, Hubert Löwenheim	2012	24
7	Genes methylated by DNA methyltransferase 3b are similar in mouse intestine and human colon cancer Journal of Clinical Investigation ·Eveline J. Steine, Mathias Ehrich, George W. Bell, Arjun Raj, Logyca, Alexander van Oudenaarden, Rudolf Jaenisch, Heinz Linhart	2011	55
8	Restriction Enzyme–Mediated Enhanced Detection of Circulating Cell-Free Fetal DNA in Maternal Plasma Journal of Molecular Diagnostics ·John A. Tynan, Payam Mahboubi, WentaoHUANG, Dirk van den Boom, Mathias Ehrich, Paul Oeth	2011	15
9	DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study Genetics in Medicine ·Glenn E. Palomaki, Edward M. Kloza, Geralyn Lambert‐Messerlian, James E. Haddow, Louis M. Neveux, Mathias Ehrich, Dirk van den Boom, Allan T. Bombard, Cosmin Deciu, Wayne W. Grody, Stanley F. Nelson, Jacob A. Canick Hit paper breakdown →	2011	660
10	General Transcription Factor Binding at CpG Islands in Normal Cells Correlates with Resistance to De novo DNA Methylation in Cancer Cells Cancer Research ·Claudia Gebhard, Christopher Benner, Mathias Ehrich, Lucia Schwarzfischer, Elmar Schilling, Maja Klug, Wolfgang Dietmaier, Christian Thiede, Ernst Holler, Reinhard Andreesen, Michael Rehli	2010	96
11	Multiplexed analysis of circulating cell-free fetal nucleic acids for noninvasive prenatal diagnostic RHD testing American Journal of Obstetrics and Gynecology ·John A. Tynan, Vach Angkachatchai, Mathias Ehrich, Toni Paladino, Dirk van den Boom, Paul Oeth	2010	30
12	Peripheral blood leukocyte distribution and body mass index are associated with the methylation pattern of the androgen receptor promoter Endocrine ·Sofia Movérare‐Skrtic, Dan Mellström, Liesbeth Vandenput, Mathias Ehrich, Claes Ohlsson	2009	17
13	Hypermethylation of Genes for Diagnosis and Risk Stratification of Prostate Cancer Cancer Investigation ·Donkena Krishna Vanaja, Mathias Ehrich, Dirk van den Boom, John C. Cheville, R. Jeffrey Karnes, Donald J. Tindall, Charles R. Cantor, Charles Y.F. Young	2009	117
14	Wnt inhibitory factor 1 is epigenetically silenced in human osteosarcoma, and targeted disruption accelerates osteosarcomagenesis in mice Journal of Clinical Investigation ·Maya Kansara, Michael Tsang, Laurent Kodjabachian, Natalie A. Sims, Melanie Trivett, Mathias Ehrich, Alexander Dobrovic, John Slavin, Peter Choong, Paul J. Simmons, Igor B. Dawid, David M. Thomas	2009	227
15	Epithelial Progeny of Estrogen-Exposed Breast Progenitor Cells Display a Cancer-like Methylome Cancer Research ·Alfred S.L. Cheng, Aedín C. Culhane, Michael W.Y. Chan, Chinnambally Venkataramu, Mathias Ehrich, Aejaz Nasir, Blanca Rodríguez, Joseph K. Liu, Pearlly S. Yan, John Quackenbush, Kenneth P. Nephew, Timothy J. Yeatman, Tim H-M. Huang	2008	112
16	Mass Spectrometric Analysis of Cytosine Methylation by Base-Specific Cleavage and Primer Extension Methods Methods in molecular biology ·Dirk van den Boom, Mathias Ehrich	2008	31
17	Dnmt3b promotes tumorigenesis in vivo by gene-specific de novo methylation and transcriptional silencing Genes & Development ·Heinz Linhart, Haijiang Lin, Yasuhiro Yamada, Eva Morán, Eveline J. Steine, Sumita Gokhale, Xiang‐Yang Xiao, G GORTVAI, Mathias Ehrich, Timothy He, Alex Meissner, Rudolf Jaenisch	2007	217
18	Discovery and Identification of Sequence Polymorphisms and Mutations with MALDI-TOF MS Methods in molecular biology ·Dirk van den Boom, Mathias Ehrich	2007	21
19	A new method for accurate assessment of DNA quality after bisulfite treatment Nucleic Acids Research ·Mathias Ehrich, Lee Bacon, Alisa Wickliff, Dirk van den Boom	2007	91
20	Cytosine Methylation Profiles as a Molecular Marker in Non–Small Cell Lung Cancer Cancer Research ·Mathias Ehrich, John K. Field, Triantafillos Liloglou, George Xinarianos, Paul Oeth, Matthew R. Nelson, Charles R. Cantor, Dirk van den Boom	2006	47

About Mathias Ehrich

Mathias Ehrich is a scholar working on Pediatrics, Perinatology and Child Health, Cancer Research, Genetics, Molecular Biology and Infectious Diseases, having authored 61 papers that have together received 6.2k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (30 papers), Epigenetics and DNA Methylation (23 papers), Fetal and Pediatric Neurological Disorders (15 papers), Cancer Genomics and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (10 papers), Genetic Syndromes and Imprinting (8 papers), Parvovirus B19 Infection Studies (8 papers) and Cancer-related gene regulation (8 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (2.9k citations), Cancer Research (1.0k citations), Infectious Diseases (1.1k citations), Genetics (1.4k citations) and Molecular Biology (3.3k citations). Mathias Ehrich has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Dirk van den Boom, Cosmin Deciu, Allan T. Bombard, Charles R. Cantor, Glenn E. Palomaki, Jacob A. Canick, Edward M. Kloza, Geralyn Lambert‐Messerlian, James E. Haddow and Matthew R. Nelson. Their work appears in journals such as Clinical Chemistry, American Journal of Obstetrics and Gynecology, Prenatal Diagnosis, Genetics in Medicine and Oncogene.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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