Publications by authors named "Jennifer Sanmann"

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A ValMet polymorphism is associated with weaker somatosensory cortical activity in individuals with cerebral palsy.
Michael Trevarrow, Jennifer N Sanmann, Tony W Wilson, Max J Kurz

Heliyon· September 2022

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Val66Met Polymorphism Is Associated with Altered Motor-Related Oscillatory Activity in Youth with Cerebral Palsy.
Michael P Trevarrow, Hannah Bergwell, Jennifer Sanmann, Tony W Wilson, Max J Kurz

Brain Sci· March 2022

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Frequency, variations, and prognostic implications of chromosome 14q32 deletions in chronic lymphocytic leukemia.
Rachel A Harris, Jadd M Stevens, Diane L Pickering, Pamela A Althof, Lynette M Smith, Jennifer N Sanmann

Leuk Res· November 2021

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A novel MYC-non-IG fusion in refractory diffuse large B-cell lymphoma.
Cheng Wang, Pamela A Althof, Chengfeng Bi, Weiwei Zhang, Alyssa C Bouska, Jennifer N Sanmann

Br J Haematol· June 2021

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Vascular dissection in women with Turner syndrome.
Anji T Yetman, Karl Stessy M Bisselou, Jennifer N Sanmann, Renee J Katz, Catherine J Steingraeber

Int J Cardiol· February 2021

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The QT Interval in Patients With the Turner Syndrome.
Noah J Harrahill, Anji T Yetman, David A Danford, Lois J Starr, Jennifer N Sanmann

Am J Cardiol· February 2021

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Additional comments regarding IGH studies in multiple myeloma.
Scott C Smith, Pamela A Althof, Bhavana J Dave, Jennifer N Sanmann

Genes Chromosomes Cancer· January 2021

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High-risk cytogenetics in multiple myeloma: Further scrutiny of deletions within the IGH gene region enhances risk stratification.
Scott C Smith, Pamela A Althof, Bhavana J Dave, Jennifer N Sanmann

Genes Chromosomes Cancer· October 2020

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The recurrent TUBB3 Gly98Ser substitution is the first described to inconsistently result in CFEOM3.
Scott C Smith, Ann Haskins Olney, Angela Beavers, Joanna Spaulding, Marilu Nelson, Jennifer N Sanmann

Am J Med Genet A· September 2020

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MECOM rearrangement involving the MYC locus: Two additional patients with the rare translocation, t(3;8)(q26.2;q24), and molecular review.
Scott C Smith, Tareq Z S Qdaisat, Pamela A Althof, Bhavana J Dave, Jennifer N Sanmann

Leuk Res· August 2020

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First report of de novo 12q14.2-q23.3 duplication: patient with multiple congenital anomalies, neurodevelopmental delay, and a connective tissue disorder-like phenotype including cutis laxa.
Rohan Khazanchi, Anji T Yetman, Jennifer N Sanmann, Lois J Starr

Clin Dysmorphol· July 2020

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Valve-Sparing Root and Total Arch Replacement for Cutis Laxa Aortopathy.
Anji T Yetman, James Hammel, Jennifer N Sanmann, Lois J Starr

World J Pediatr Congenit Heart Surg· May 2019

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Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar.
Erin R Riggs, Tristan Nelson, Andrew Merz, Todd Ackley, Brian Bunke, Jennifer N Sanmann

Hum Mutat· November 2018

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Lymphomas with pseudo-double-hit BCL6-MYC translocations due to t(3;8)(q27;q24) are associated with a germinal center immunophenotype, extranodal involvement, and frequent BCL2 translocations.
Steven M Johnson, Jayadev Manikkam Umakanthan, Ji Yuan, Yuri Fedoriw, R Gregory Bociek, Jennifer N Sanmann

Hum Pathol· October 2018

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Clinical and Echocardiographic Prevalence and Detection of Congenital and Acquired Cardiac Abnormalities in Girls and Women with the Turner Syndrome.
Anji T Yetman, Lois Starr, Jennifer Sanmann, Megan Wilde, Mary Murray

Am J Cardiol· July 2018

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Bariatric Implant-Associated Anaplastic Large-Cell Lymphoma.
Jayadev Manikkam Umakanthan, Corrigan L McBride, Timothy Greiner, Ji Yuan, Jennifer Sanmann

J Oncol Pract· December 2017

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Mammary analog secretory carcinoma, low-grade salivary duct carcinoma, and mimickers: a comparative study.
Todd M Stevens, Andra O Kovalovsky, Claudia Velosa, Qiuying Shi, Qian Dai, Jennifer N Sanmann

Mod Pathol· February 2017

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ALK-positive Large B-cell Lymphoma: A Clinicopathologic Study of 26 Cases With Review of Additional 108 Cases in the Literature.
Zenggang Pan, Shimin Hu, Min Li, Yi Zhou, Young S Kim, Jennifer N Sanmann

Am J Surg Pathol· January 2017

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The first patient with tandem duplication of 6q14q16: Molecular and phenotypic characterization.
Jennifer N Sanmann, Kari A Casas, Jen Bevilacqua, Danielle L Bishay, Tanner Clark

Am J Med Genet A· September 2016

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Karyotypic abnormalities associated with Epstein-Barr virus status in classical Hodgkin lymphoma.
Nathan D Montgomery, Wilborn B Coward, Steven Johnson, Ji Yuan, Margaret L Gulley, Jennifer N Sanmann

Cancer Genet· September 2016

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Myhre syndrome: Clinical features and restrictive cardiopulmonary complications.
Lois J Starr, Dorothy K Grange, Jeffrey W Delaney, Anji T Yetman, James M Hammel, Jennifer N Sanmann

Am J Med Genet A· December 2015

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A formalin-free method for stabilizing cells for nucleic acid amplification, hybridization and next-generation sequencing.
Jianbing Qin, Jennifer N Sanmann, Jeff S Kittrell, Pamela A Althof, Erin E Kaspar

BMC Res Notes· December 2015

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Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarray.
Jennifer N Sanmann, Diane L Pickering, Denae M Golden, Jadd M Stevens, Thomas E Hempel

Genet Med· November 2015

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Mammary analog secretory carcinoma, low-grade salivary duct carcinoma, and mimickers: a comparative study.
Todd M Stevens, Andra O Kovalovsky, Claudia Velosa, Qiuying Shi, Qian Dai, Jennifer N Sanmann

Mod Pathol· August 2015

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In Memoriam: Warren G. Sanger, PhD (October 6, 1945-February 5, 2015).
Jennifer N Sanmann, Loris McGavran, Shivanand R Patil

Cancer Genet· April 2015

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