Thomas Scholl

5.2k citations

46 papers · 2.5k indexed · 1 hit paper · h-index 20

Impact in

Genetics top 2%
- BRCA gene mutations in cancer
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
Cancer Research top 5%
- Cancer Genomics and Diagnostics

Papers in

Genetics 14
- BRCA gene mutations in cancer 10
- Genomic variations and chromosomal abnormalities 8
Gastroenterology 2

Co-authors: Brian E. Ward Amie M. Deffenbaugh Jack L. Strominger S. Mahanta Julia Reid Viatcheslav R. Akmaev Brant C. Hendrickson Dmitry Pruss
Journals: Proceedings of the National Academy of Sciences (3 papers)Archiv der Pharmazie (2 papers)Cancer Research (2 papers)Molecular Genetics and Metabolism (2 papers)Journal of Clinical Oncology (2 papers)
Partner nations: United States Germany United Kingdom

In The Last Decade

Thomas Scholl

46 papers receiving 2.5k citations

Hit Papers

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Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens 2011 · 457 citations

Peers

Countries citing papers authored by Thomas Scholl

Since Specialization

Citations

This map shows the geographic impact of Thomas Scholl'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 Thomas Scholl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Scholl more than expected).

Fields of papers citing papers by Thomas Scholl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas Scholl. 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 Thomas Scholl. The network helps show where Thomas Scholl may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Thomas Scholl, 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 Thomas Scholl Line = papers co-authored together Thomas Scholl links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A GC-Wave Correction Algorithm that Improves the Analytical Performance of aCGH Journal of Molecular Diagnostics ·Angela Leo, A. M. Walker, Matthew S. Lebo, Brant C. Hendrickson, Thomas Scholl, Viatcheslav R. Akmaev	2012	6
2	Late angiotensin II receptor blockade in progressive rat mesangioproliferative glomerulonephritis: new insights into mechanisms The Journal of Pathology ·Luigi Villa, Peter Boor, Andrzej Konieczny, Uta Kunter, O. Pidkuiko, Bernd Denecke, Lin Gan, Matthias A. Neusser, Clemens D. Cohen, Frank Eitner, Thomas Scholl, Tammo Ostendorf, Jürgen Floege	2012	11
3	Development of a Pompe disease CRIM assay for blood samples Molecular Genetics and Metabolism ·Joan Keutzer, Zhaohui Wang, Patricia M. Okamoto, Thomas Scholl	2011	2
4	BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast‐ovarian cancer Cancer ·Michael J. Hall, Julia Reid, Lynn Anne Burbidge, Dmitry Pruss, Amie M. Deffenbaugh, Cynthia Frye, Richard Wenstrup, Brian E. Ward, Thomas Scholl, Walter W. Noll	2009	275
5	Genetic heterozygosity and pseudodeficiency in the Pompe disease newborn screening pilot program Molecular Genetics and Metabolism ·Tavernier T., Yin‐Hsiu Chien, Robert J. Pomponio, Joan Keutzer, Ni‐Chung Lee, Viatcheslav R. Akmaev, Thomas Scholl, Wuh‐Liang Hwu	2009	77
6	Multiple Rare Nonsynonymous Variants in the Adenomatous Polyposis Coli Gene Predispose to Colorectal Adenomas Cancer Research ·Jared B. Baylis, Anthony R. Dallosso, Kristilyn Eliason, Brant C. Hendrickson, Natalie Jones, Freya Ponteur, James Colley, Valentina Moskvina, Cynthia Frye, Julian R. Sampson, Richard Wenstrup, Thomas Scholl, Jeremy P. Cheadle	2008	68
7	Prediction of MLH1 and MSH2 Mutations in Lynch Syndrome JAMA ·Judith Balmañà, David H. Stockwell, Ewout W. Steyerberg, Elena M. Stoffel, Amie M. Deffenbaugh, Julia Reid, Brian E. Ward, Thomas Scholl, Brant C. Hendrickson, John Tazelaar, Lynn Anne Burbidge, Sapna Syngal	2006	135
8	Single nucleotide polymorphisms in clinical genetic testing: the characterization of the clinical significance of genetic variants and their application in clinical research for BRCA1 Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Thaddeus Judkins, Brant C. Hendrickson, Amie M. Deffenbaugh, Thomas Scholl	2005	17
9	A Multi-Exonic BRCA1 Deletion Identified in Multiple Families through Single Nucleotide Polymorphism Haplotype Pair Analysis and Gene Amplification with Widely Dispersed Primer Sets Journal of Molecular Diagnostics ·Benjamin D. Ward, Brant C. Hendrickson, Thaddeus Judkins, Amie M. Deffenbaugh, Benoît Leclair, Brian E. Ward, Thomas Scholl	2005	8
10	Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families Genes Chromosomes and Cancer ·Brant C. Hendrickson, Thaddeus Judkins, Benjamin D. Ward, Kristilyn Eliason, Patrycja Ewelina Romanowska, Lynn Anne Burbidge, A Mascaut, Benoît Leclair, Brian E. Ward, Thomas Scholl	2005	43
11	A Biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A→C is a mutation Journal of Human Genetics ·Ida Pind, David R. Nielsen, Brant C. Hendrickson, Michael T. Pyne, Lauren Scheuer, Brian E. Ward, Arthur R. Brothman, Thomas Scholl	2003	13
12	Shared Genetic Susceptibility to Breast Cancer, Brain Tumors, and Fanconi Anemia JNCI Journal of the National Cancer Institute ·Kenneth Offit, Orna Levran, Brendan Mullaney, Kandice Mah, Khédoudja Nafa, Sat Dev Batish, Roberta A. Diotti, A B Vaidya, Amie M. Deffenbaugh, Thomas Scholl, V. Proud, Mark E. Robson, Larry Norton, Nathan A. Ellis, Helmut Hanenberg, Arleen D. Auerbach	2003	122
13	A zinc finger protein that represses transcription of the human MHC class II gene, DPA The Journal of Immunology ·Thomas Scholl, José Luis Priego Fernández del Campo, S. Mahanta, Jack L. Strominger	1996	39
14	Cooperativity between the J and S elements of class II major histocompatibility complex genes as enhancers in normal and class II-negative patient and mutant B cell lines. The Journal of Experimental Medicine ·Mitsuru Sugawara, Thomas Scholl, S. Mahanta, Paul Ponath, J L Strominger	1995	6
15	A Factor That Regulates the Class II Major Histocompatibility Complex Gene DPA Is a Member of a Subfamily of Zinc Finger Proteins That Includes a Drosophila Developmental Control Protein Molecular and Cellular Biology ·Minoru Sugawara, Thomas Scholl, Paul Ponath, Jack L. Strominger	1994	18
16	Hypomethylation of MHC class II Eb gene is associated with expression Immunogenetics ·Thomas Scholl, Sri Khairiani, Barry Jones	1992	4
17	2-[(2-Pyridylmethyl)sulfinyl]-1H-thieno[3,4-d]imidazoles. A novel class of gastric H+/K+-ATPase inhibitors Journal of Medicinal Chemistry ·د وائل السید العبد خلیفة, Andreas W. Herling, Hans J. Lang, Liliana Montoya Vélez, 梁伟波, Hildegard Nimmesgern, Thomas Scholl, M. Bickel, H. Metzger	1992	19
18	Gastric Acid Inhibitory Profile of Saviprazole (HOE 731) Compared to Omeprazole Pharmacology ·Andreas W. Herling, Thomas Scholl, Martin Bickel, 陈晶莹, Liliana Montoya Vélez, د وائل السید العبد خلیفة, 梁伟波	1991	4
19	The inhibitory effect of HOE 731 in isolated rabbit gastric glands Biochemical Pharmacology ·Andreas W. Herling, Αγάθη Βρεττού, 陈晶莹, Liliana Montoya Vélez, د وائل السید العبد خلیفة, Thomas Scholl, 梁伟波	1990	2
20	Virus-specific cellular blastogenesis and interleukin-2 production in swine after recovery from African swine fever American Journal of Veterinary Research ·Thomas Scholl, Joan K. Lunney, Charles A. Mebus, 香川聖子, Carlos Martins	1989	24

About Thomas Scholl

Thomas Scholl is a scholar working on Genetics, Gastroenterology, Molecular Biology, Pharmaceutical Science and Immunology, having authored 46 papers that have together received 2.5k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Genomic variations and chromosomal abnormalities (8 papers), CRISPR and Genetic Engineering (7 papers), Immune Cell Function and Interaction (5 papers), T-cell and B-cell Immunology (5 papers), RNA and protein synthesis mechanisms (4 papers), Genetic factors in colorectal cancer (4 papers) and Synthesis and Properties of Aromatic Compounds (3 papers). The work is most often cited by research in Genetics (457 citations), Genetics (1.0k citations), Cancer Research (371 citations), Pathology and Forensic Medicine (318 citations) and Molecular Biology (1.1k citations). Thomas Scholl has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Brian E. Ward, Amie M. Deffenbaugh, Jack L. Strominger, S. Mahanta, Julia Reid, Viatcheslav R. Akmaev, Brant C. Hendrickson, Dmitry Pruss, Kerry L. Flynn and Narasimhan Nagan. Their work appears in journals such as Proceedings of the National Academy of Sciences, Archiv der Pharmazie, Cancer Research, Molecular Genetics and Metabolism and Journal of Clinical Oncology.

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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