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35 publications found

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Group #1

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Obesity rather than neoadjuvant chemotherapy predicts steatohepatitis in patients with colorectal metastasis[1]Matthew Bower, [2]Chris Wunderlich, [3]Russell Brown, [4]Charles R. Scoggins, [5]Kelly M. McMasters, [6]Robert C G Martin [Full author list]The American Journal of Surgery [missing]DOI: 10.1016/J.AMJSURG.2012.07.034 [ORCID]
PubMed: 23388422 [ORCID]
obesity [missing]; steatohepatitis [missing]2013-02-04
The lower incidence of melanoma in women may be related to increased preventative behaviors[1]Nathaniel P Reuter, [2]Matthew Bower, [3]Charles R. Scoggins, [4]Robert C G Martin, [5]Kelly M. McMasters, [6]Anees B Chagpar [Full author list]The American Journal of Surgery [missing]DOI: 10.1016/J.AMJSURG.2010.06.007 [ORCID]
PubMed: 21146018 [ORCID]
2010-12-01
Hepatectomy is superior to thermal ablation for patients with a solitary colorectal liver metastasis[1]Suzanne Claire Schiffman, [2]Matthew Bower, [3]Russell E Brown, [4]Robert C G Martin, [5]Kelly M. McMasters, [6]Charles R. Scoggins [Full author list]Journal of Gastrointestinal Surgery [missing]DOI: 10.1007/S11605-010-1339-Z [ORCID]
PubMed: 20859701 [ORCID]
hepatectomy [missing]2010-09-22
Role of esophageal stents in the nutrition support of patients with esophageal malignancy[1]Matthew Bower, [2]Whitney Jones, [3]Ben Vessels, [4]Charles R. Scoggins, [5]Robert C G Martin [Full author list]Nutrition in Clinical Practice [missing]DOI: 10.1177/0884533610368710 [ORCID]
PubMed: 20581317 [ORCID]
2010-06-01
Surgical downstaging and neo-adjuvant therapy in metastatic colorectal carcinoma with irinotecan drug-eluting beads: a multi-institutional study[1]Matthew Bower, [2]Tiffany Metzger, [3]Ken Robbins, [4]Dana Tomalty, [5]Vlatimil Válek, [6]Jean Boudný, [7]Tomas Andrasina, [8]Cliff Tatum, [9]Robert C G Martin [Full author list]Hepato Pancreato Biliary [missing]DOI: 10.1111/J.1477-2574.2009.00117.X [ORCID]
PubMed: 20495642 [ORCID]
irinotecan [missing]; metastatic colorectal carcinoma [missing]2010-02-01
Nutritional support with endoluminal stenting during neoadjuvant therapy for esophageal malignancy[1]Matthew Bower, [2]Whitney Jones, [3]Ben Vessels, [4]Charles R. Scoggins, [5]Robert C G Martin [Full author list]Annals of Surgical Oncology [missing]DOI: 10.1245/S10434-009-0630-2 [ORCID]
PubMed: 19636630 [ORCID]
2009-07-28
Sentinel lymphadenectomy for cutaneous melanoma: who, what, and why[1]Matthew Bower, [2]Charles R. Scoggins [Full author list]Journal of the Kentucky Medical Association [missing]PubMed: 19678500 [ORCID]
lymphadenectomy [missing]2009-07-01

Group #2

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification[1]Sandy Chan Hsu, [2]Renee L. Sears, [3]Roberta R Lemos, [4]Beatriz Quintáns, [5]Alden Huang, [6]Elizabeth Spiteri, [7]Lisette Nevarez, [8]Catherine Mamah, [9]Mayana Zatz, [10]Kerrie D Pierce, ..., [12]John C Adair, [13]Jon E Berner, [14]Matthew Bower, [15]Henry Brodaty, [16]Olga Carmona, ... [Full author list]Neurogenetics [missing]DOI: 10.1007/S10048-012-0349-2 [ORCID]
PubMed: 23334463 [ORCID]
2013-01-20
Clinical and pathologic evidence of corticobasal degeneration and progressive supranuclear palsy in familial tauopathy[1]Paul Tuite, [2]H Brent Clark, [3]Catherine Bergeron, [4]Matthew Bower, [5]Peter Henry St George-Hyslop, [6]Vesselina Mateva, [7]John Anderson, [8]David S Knopman [Full author list]Archives of Neurology [missing]DOI: 10.1001/ARCHNEUR.62.9.1453 [ORCID]
PubMed: 16157754 [ORCID]
progressive supranuclear palsy [missing]; tauopathy [missing]2005-09-01

Group #3

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Next generation sequencing for clinical diagnostics: Five year experience of an academic laboratory[1]Paige Hartman, [2]Kenneth Beckman, [3]Kevin A. T. Silverstein, [4]Sophia Yohe, [5]Matthew Schomaker, [6]Christine Henzler, [7]Getiria Onsongo, [8]Ham Ching Lam, [9]Sarah Munro, [10]Jerry Daniel, ..., [23]Venugopal Thayanithy, [24]Andrew Nelson, [25]Matthew Bower, [26]Bharat Thyagarajan [Full author list]Molecular Genetics and Metabolism Reports [missing]DOI: 10.1016/J.YMGMR.2019.100464 [ORCID]
PubMed: 30891420 [ORCID]
2019-03-01
CNV-RF Is a Random Forest-Based Copy Number Variation Detection Method Using Next-Generation Sequencing[1]Getiria Onsongo, [2]Linda B Baughn, [3]Matthew Bower, [4]Christine Henzler, [5]Matthew Schomaker, [6]Kevin A T Silverstein, [7]Bharat Thyagarajan [Full author list]The Journal of Molecular Diagnostics [missing]DOI: 10.1016/J.JMOLDX.2016.07.001 [ORCID]
PubMed: 27597741 [ORCID]
random forest [missing]2016-09-02
65: Incidental Genetic Findings and Patient Preferences Regarding Return of Results in a Population of Patients With Unexplained Ataxia Undergoing Next-Generation Sequencing[1]Katie Wiens, [2]Matthew Bower, [3]Khalaf Bushara, [4]Bharat Thyagarajan [Full author list]American Journal of Clinical Pathology [missing]DOI: 10.1093/AJCP/143.SUPPL1.038 [ORCID]
2015-05-01
Clinical validation of targeted next-generation sequencing for inherited disorders[1]Sophia Yohe, [2]Adam Hauge, [3]Kari Bunjer, [4]Teresa Kemmer, [5]Matthew Bower, [6]Matthew Schomaker, [7]Getiria Onsongo, [8]Jon Wilson, [9]Jesse Erdmann, [10]Yi Zhou, [11]Archana Deshpande, [12]Michael D Spears, [13]Kenneth Beckman, [14]Kevin A T Silverstein, [15]Bharat Thyagarajan [Full author list]Archives of Pathology & Laboratory Medicine [missing]DOI: 10.5858/ARPA.2013-0625-OA [ORCID]
PubMed: 25611102 [ORCID]
2015-02-01
Implementation of Cloud based next generation sequencing data analysis in a clinical laboratory[1]Getiria Onsongo, [2]Jesse Erdmann, [3]Michael D Spears, [4]John Chilton, [5]Kenneth B Beckman, [6]Adam Hauge, [7]Sophia Yohe, [8]Matthew Schomaker, [9]Matthew Bower, [10]Kevin A T Silverstein, [11]Bharat Thyagarajan [Full author list]BMC Research Notes [missing]DOI: 10.1186/1756-0500-7-314 [ORCID]
PubMed: 24885806 [ORCID]
data analysis [missing]2014-05-23
CLIA-certified next-generation sequencing analysis in the cloud[1]Ying Zhang, [2]Jesse Erdmann, [3]John Chilton, [4]Getiria Onsongo, [5]Matthew Bower, [6]Kenny Beckman, [7]Bharat Thyagarajan, [8]Kevin Silverstein, [9]Anne-Francoise Lamblin [Full author list]BMC Proceedings [missing]DOI: 10.1186/1753-6561-6-S6-P54 [ORCID]
2012-10-01
A novel polymorphism in the FMR1 gene: implications for clinical testing of fragile X syndrome.[1]Bharat Thyagarajan, [2]Matthew Bower, [3]Michael Berger, [4]Sidney Jones, [5]Michelle Dolan, [6]Xinjing Wang [Full author list]Archives of Pathology & Laboratory Medicine [missing]PubMed: 18181681 [ORCID]
fragile X syndrome [missing]2008-01-01

Group #4

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnostics[1]Dimitre R. Simeonov, [2]Xinjing Wang, [3]Chen Wang, [4]Yuri Sergeev, [5]Monika Dolinska, [6]Matthew Bower, [7]Roxanne Fischer, [8]David Winer, [9]Genia Dubrovsky, [10]Joan Z. Balog, [11]Marjan Huizing, [12]Rachel Hart, [13]Wadih M. Zein, [14]William A. Gahl, [15]Brian P. Brooks, [16]David R. Adams [Full author list]Human Mutation [missing]DOI: 10.1002/HUMU.22315 [ORCID]
PubMed: 23504663 [ORCID]
oculocutaneous albinism [missing]2013-06-01
Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database[1]Matthew Bower, [2]Rémi Salomon, [3]Judith Allanson, [4]Corinne Antignac, [5]Francesco Benedicenti, [6]Elisa Benetti, [7]Gil Binenbaum, [8]Uffe Birk Jensen, [9]Pierre Cochat, [10]Stephane DeCramer, ... [Full author list]Human Mutation [missing]DOI: 10.1002/HUMU.22020 [ORCID]
PubMed: 22213154 [ORCID]
database [missing]; renal coloboma syndrome [missing]2012-01-31
Clinical utility gene card for: renal coloboma (Papillorenal) syndrome[1]Matthew Bower, [2]Michael Eccles, [3]Laurence Heidet, [4]Lisa A Schimmenti [Full author list]European Journal of Human Genetics [missing]DOI: 10.1038/EJHG.2011.16 [ORCID]
PubMed: 21326282 [ORCID]
2011-02-16

Group #5

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spot[1]Charlotte A Brown, [2]Juergen Scharner, [3]Kevin Felice, [4]Matthew N Meriggioli, [5]Mark Tarnopolsky, [6]Matthew Bower, [7]Peter S Zammit, [8]Jerry R Mendell, [9]Juliet A Ellis [Full author list]Journal of Human Genetics [missing]DOI: 10.1038/JHG.2011.65 [ORCID]
PubMed: 21697856 [ORCID]
Emery-Dreifuss muscular dystrophy [missing]2011-06-23
Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations[1]Juergen Scharner, [2]Charlotte A Brown, [3]Matthew Bower, [4]Susan T. Iannaccone, [5]Ismail A Khatri, [6]Diana Escolar, [7]Erynn Gordon, [8]Kevin Felice, [9]Carol A Crowe, [10]Carla Grosmann, [11]Matthew N Meriggioli, [12]Alexander Asamoah, [13]Ora Gordon, [14]Viola F Gnocchi, [15]Juliet A Ellis, [16]Jerry R Mendell, [17]Peter S Zammit [Full author list]Human Mutation [missing]DOI: 10.1002/HUMU.21361 [ORCID]
PubMed: 20848652 [ORCID]
Emery-Dreifuss muscular dystrophy [missing]2011-01-25

Group #6

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Ethical and Professional Challenges Encountered by Laboratory Genetic Counselors.[1]Daniel Groepper, [2]Patricia McCarthy Veach, [3]Bonnie S LeRoy, [4]Matthew Bower [Full author list]Journal of Genetic Counseling [missing]DOI: 10.1007/S10897-014-9787-3 [ORCID]
PubMed: 25398381 [ORCID]
2014-11-16
Prenatal chromosomal microarray analysis: a survey of prenatal genetic counselors' experiences and attitudes[1]Marina Mikhaelian, [2]Patricia McCarthy Veach, [3]Ian MacFarlane, [4]Bonnie S LeRoy, [5]Matthew Bower [Full author list]Prenatal Diagnosis [missing]DOI: 10.1002/PD.4071 [ORCID]
PubMed: 23450520 [ORCID]
2013-03-01

Misc

Matched potential author: Matthew M Bower - author of 6 items
TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Case Report: Early-Onset Behavioral Variant Frontotemporal Dementia in Patient With Retrotransposed Full-Length Transcript of Matrin-3 Variant 5[1]Madelyn Castro, [2]Nisha Venkateswaran, [3]Samuel T Peters, [4]David R Deyle, [5]Matthew Bower, [6]Michael D Koob, [7]Bradley F Boeve, [8]Keith Vossel [Full author list]Frontiers in Neurology [missing]DOI: 10.3389/FNEUR.2020.600468 [ORCID]
PubMed: 33408686 [ORCID]
frontotemporal dementia [missing]2020-12-21
Early Initiation of Oral Antihypertensives Reduces Intensive Care Unit Stay and Hospital Cost for Patients with Hypertensive Intracerebral Hemorrhage[1]Zhu Zhu, [2]Matthew Bower, [3]Sara Stern-Nezer, [4]Steven Atallah, [5]Dana Stradling, [6]Leonid Groysman, [7]Cyrus K Dastur, [8]Yama Akbari, [9]Wengui Yu [Full author list]Neurocritical Care [missing]DOI: 10.1007/S12028-020-00951-1 [ORCID]
PubMed: 32253732 [ORCID]
intensive care unit [missing]2020-04-06Matthew M Bower (Q83521301; 6 items)
A homozygous frameshift variant in the KRT5 gene is compatible with life and results in severe recessive epidermolysis bullosa simplex[1]Rebecca K Tryon, [2]Jakub Tolar, [3]Sarah M Preusser, [4]Megan J Riddle, [5]Douglas R Keene, [6]Matthew Bower, [7]Bharat Thyagarajan, [8]Christen L Ebens [Full author list]JAAD case reports [missing]DOI: 10.1016/J.JDCR.2019.03.025 [ORCID]
PubMed: 31312705 [ORCID]
epidermolysis bullosa simplex [missing]; homozygosity [missing]2019-06-26
Mosaicism of the UDP-Galactose transporter SLC35A2 in a female causing a congenital disorder of glycosylation: a case report[1]Kristen Westenfield, [2]Kyriakie Sarafoglou, [3]Laura C Speltz, [4]Elizabeth I Pierpont, [5]Joan Steyermark, [6]David R Nascene, [7]Matthew Bower, [8]Mary Ella Pierpont [Full author list]BMC Medical Genetics [missing]DOI: 10.1186/S12881-018-0617-6 [ORCID]
PubMed: 29907092 [ORCID]
congenital disorder [missing]; glycosylation [missing]; congenital disorder of glycosylation [missing]; congenital disorder [missing]2018-06-15
Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies[1]Claire G Salter, [2]Danique Beijer, [3]Holly Hardy, [4]Katy E S Barwick, [5]Matthew Bower, [6]Ines Mademan, [7]Peter De Jonghe, [8]Tine Deconinck, [9]Mark A Russell, [10]Meriel M McEntagart, [11]Barry A Chioza, [12]Randy D Blakely, [13]John K Chilton, [14]Jan De Bleecker, [15]Jonathan Baets, [16]Emma L Baple, [17]David Walk, [18]Andrew H Crosby [Full author list]Neurology. Genetics [missing]DOI: 10.1212/NXG.0000000000000222 [ORCID]
PubMed: 29582019 [ORCID]
2018-03-23
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy[1]Yanyan Peng, [2]Deepali N Shinde, [3]C Alexander Valencia, [4]Jun-Song Mo, [5]Jill Rosenfeld, [6]Megan Truitt Cho, [7]Adam Chamberlin, [8]Zhuo Li, [9]Jie Liu, [10]Baoheng Gui, ..., [18]Solange Gril, [19]Shuk Ching Chong, [20]Matthew Bower, [21]Kristin G Monaghan, [22]Rebecca Willaert, ... [Full author list]Human Molecular Genetics [missing]DOI: 10.1093/HMG/DDX377 [ORCID]
PubMed: 29040572 [ORCID]
2017-12-01
Genetic Testing for Deaf and Hard of Hearing Individuals: Genetic Counseling[1]Lisa A. Schimmenti, [2]Joan Steyermark, [3]Matthew Bower [Full author list]Current genetic medicine reports [missing]DOI: 10.1007/S40142-016-0089-Y [ORCID]
2016-04-01
Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry[1]Khalaf Bushara, [2]Matthew Bower, [3]Jilin Liu, [4]Karen N McFarland, [5]Ivette Landrian, [6]Diane Hutter, [7]Hélio A G Teive, [8]Astrid Rasmussen, [9]Connie J Mulligan, [10]Tetsuo Ashizawa [Full author list]PLOS One [missing]DOI: 10.1371/JOURNAL.PONE.0081342 [ORCID]
PubMed: 24278426 [ORCID]
spinocerebellar ataxia type 10 [missing]2013-11-20
Detection of PAX2 deletions and duplications using multiplex ligation-dependent probe amplification[1]Amy B Karger, [2]Jon D Wilson, [3]Matthew Bower, [4]Lisa A Schimmenti, [5]Bharat Thyagarajan [Full author list]Genetic Testing and Molecular Biomarkers [missing]DOI: 10.1089/GTMB.2013.0176 [ORCID]
PubMed: 23756089 [ORCID]
2013-06-11
Irreversible electroporation of the pancreas: definitive local therapy without systemic effects[1]Matthew Bower, [2]Leslie Sherwood, [3]Yan Li, [4]Robert Martin [Full author list]Journal of Surgical Oncology [missing]DOI: 10.1002/JSO.21899 [ORCID]
PubMed: 21360714 [ORCID]
pancreas [missing]; electroporation [missing]2011-02-28
A comparison of disinfection by-products found in chlorinated and chloraminated drinking waters in Scotland[1]Emma H. Goslan, [2]Stuart W Krasner, [3]Matthew Bower, [4]Sophie A Rocks, [5]Philip Holmes, [6]Leonard S Levy, [7]Simon A Parsons [Full author list]Water Research [missing]DOI: 10.1016/J.WATRES.2009.07.029 [ORCID]
PubMed: 19665750 [ORCID]
disinfection [missing]2009-07-26
Role of the geneticist in testing and counseling for inherited thrombophilia[1]Laura M Reich, [2]Matthew Bower, [3]Nigel S Key [Full author list]Genetics in Medicine [missing]DOI: 10.1097/01.GIM.0000067987.77803.D0 [ORCID]
PubMed: 12792420 [ORCID]
thrombophilia [missing]2003-05-01

Potential author items

NameDescriptionAuthored itemsIdentifiersEmployer(s)
Matt Bowereducation researcher30ORCID: 0000-0002-4161-5816
Macquarie University [missing]
Matthew M Bowerresearcher6ORCID: 0000-0002-2753-8201
UC Irvine Health [missing]
Johns Hopkins Medicine [missing]
University of California, Irvine [missing]
Indiana University [missing]
Matthew BowerBritish musician0ISNI: 0000000465567972
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