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European Journal of Human Genetics : EJHG|March 15, 2013
Intragenic deletions of the IGF1 receptor gene in five individuals with psychiatric phenotypes and developmental delayJens Witsch, Przemyslaw Szafranski, Chun-An Chen, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 28, 2022
Diagnostic test accuracy of magnetic resonance imaging and pelvic floor ultrasound for diagnosis of levator ani muscle avulsionI M A Van Gruting, A Stankiewicz, K W M Van Delft, et al.
International Journal for Parasitology|June 26, 2008
The effect of corticosteroid treatment on local immune responses, intake and performance in lambs infected with Teladorsagia circumcinctaA W Greer, J F Huntley, A Mackellar, et al.
Molecular Genetics & Genomic Medicine|September 20, 2022
High-level gonosomal mosaicism for a pathogenic non-coding CNV deletion of the lung-specific FOXF1 enhancer in an unaffected mother of an infant with ACDMPVEsra Yıldız Bölükbaşı, Justyna A Karolak, Przemyslaw Szafranski, et al.
Cancer|November 18, 2009
Antimullerian hormone and inhibin B are hormone measures of ovarian function in late reproductive-aged breast cancer survivorsH Irene Su, Mary D Sammel, Jamie Green, et al.
Plos One|June 15, 2018
PIK3CA copy number aberration and activation of the PI3K-AKT-mTOR pathway in varied disease states of penile cancerAnthony Adimonye, Elzbieta Stankiewicz, Susannah La-Touche, et al.
Molecular Biology Reports|September 16, 2010
Polymorphisms in 5'-flanking regions of genes encoding adiponectin, leptin, and resistin are not associated with obesity of Polish children and adolescentsJakub Cieslak, Anna Skorczyk, Monika Stachowiak, et al.
Nucleic Acids Research|February 1, 1979
Comparison of rat liver and Walker 256 carcinosarcoma tRNAsB A Roe, A F Stankiewicz, H L Rizi, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|March 23, 2017
Pregnancy at Advanced Maternal Age Affects Behavior and Hippocampal Gene Expression in Mouse OffspringSilvestre Sampino, Adrian Mateusz Stankiewicz, Federica Zacchini, et al.
Clinical Genetics|June 21, 2025
Highly Variable Expressivity of a CNV Deletion Involving TBX4 in Three Deceased Siblings With Lung Developmental Disorder and Their Mildly Affected Mother and GrandfatherPrzemyslaw Szafranski, Tomasz Gambin, Michal Kadlof, et al.
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