Maciej Geremek

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 10

Top Topics

Contrast Enhanced Ultrasound

Dna Methylation

Low Birth Weight

Top Venues

Ginekologia polska

Genetics in medicine : official journal of the American College of Medical Genetics

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Marta Smyk, Maciej Geremek, Kamila Ziemkiewicz, Tomasz Gambin, Anna Kutkowska-Kaźmierczak, Katarzyna Kowalczyk, Izabela Plaskota, Barbara Wiśniowiecka-Kowalnik, Magdalena Bartnik-Głaska, Magdalena Niemiec, Dominika Grad, Małgorzata Piotrowicz, Dorota Gieruszczak-Białek, Aleksandra Pietrzyk, Terrence Blaine Crowley, Victoria Giunta, Daniel E McGinn, Elaine H Zackai, Oanh Tran, Beverly S Emanuel, Donna M McDonald-McGinn, Beata A Nowakowska
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome. Genes 14 (3) (2023)
Marta Smyk, Maciej Geremek, Kamila Ziemkiewicz, Tomasz Gambin, Anna Kutkowska-Kaźmierczak, Katarzyna Kowalczyk, Izabela Plaskota, Barbara Wiśniowiecka-Kowalnik, Magdalena Bartnik-Głaska, Magdalena Niemiec, Dominika Grad, Małgorzata Piotrowicz, Dorota Gieruszczak-Białek, Aleksandra Pietrzyk, Terrence Blaine Crowley, Victoria Giunta, Daniel E McGinn, Elaine H Zackai, Oanh Tran, Beverly S Emanuel, Donna M McDonald-McGinn, Beata A Nowakowska
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome. Genes 14 (3) (2023)
Marta Smyk, Maciej Geremek, Kamila Ziemkiewicz, Tomasz Gambin, Anna Kutkowska-Kaźmierczak, Katarzyna Kowalczyk, Izabela Plaskota, Barbara Wiśniowiecka-Kowalnik, Magdalena Bartnik-Głaska, Magdalena Niemiec, Dominika Grad, Małgorzata Piotrowicz, Dorota Gieruszczak-Białek, Aleksandra Pietrzyk, Terrence Blaine Crowley, Victoria Giunta, Daniel E McGinn, Elaine H Zackai, Oanh Tran, Beverly S Emanuel, Donna M McDonald-McGinn, Beata A Nowakowska
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome. Genes 14 (3) (2023)
Katarzyna Kowalczyk, Magdalena Bartnik-Głaska, Marta Smyk, Izabela Plaskota, Joanna Bernaciak, Marta Kędzior, Barbara Wiśniowiecka-Kowalnik, Marta Deperas, Justyna Domaradzka, Alicja Łuszczek, Daria Dutkiewicz, Agata Kozar, Dominika Grad, Magdalena Niemiec, Kamila Ziemkiewicz, Róża Magdziak, Natalia Braun-Walicka, Artur Barczyk, Maciej Geremek, Jennifer Castañeda, Anna Kutkowska-Kaźmierczak, Paweł Własienko, Krystyna Jakubów-Durska, Marzena Debska, Anna M Kucinska-Chahwan, Szymon Kozłowski, Boyana Mikulska, Tadeusz Issat, Tomasz Roszkowski, Agnieszka Nawara-Baran, Agata Runge, Anna Jakubiuk-Tomaszuk, Anna Kruczek, Ewa Kostyk, Grzegorz Pietras, Janusz Limon, Jerzy Zwoliński, Karolina Ochman, Tomasz Szajner, Malgorzata Swiatkowska-Freud, Mirosław Wielgoś, Maria Sąsiadek, Ewa Obersztyn, Beata Anna Nowakowska
Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies. Genes 13 (4) (2022)
Anna M Kucinska-Chahwan, Maciej Geremek, Tomasz Roszkowski, Julia Bijok, Diana Massalska, Michal Ciebiera, Hildeberto Correia, Iris Pereira-Caetano, Ana Barreta, Ewa Obersztyn, Anna Kutkowska-Kaźmierczak, Paweł Własienko, Malgorzata Krajewska-Walasek, Piotr Węgrzyn, Lech Dudarewicz, Waldemar Krzeszowski, Magda Rybak-Krzyszkowska, Beata Nowakowska
Implementation of Exome Sequencing in Prenatal Diagnosis and Impact on Genetic Counseling: The Polish Experience. Genes 13 (5) (2022)
Maciej Geremek, Krzysztof Szklanny
Deep Learning-Based Analysis of Face Images as a Screening Tool for Genetic Syndromes. Sensors (Basel, Switzerland) 21 (19) (2021)
Anna M Kucinska-Chahwan, Tomasz Roszkowski, Maciej Geremek, Magdalena A Paczkowska, Michal Ciebiera, Julia Bijok, Diana Massalska, Grzegorz Panek, Krzysztof Siemion, Sebastian Kwiatkowski
Prenatal diagnosis of glutaric acidemia type 2 with the use of exome sequencing - an up-to-date review and new case report. Ginekologia polska 92 (1) (2021)
Katarzyna Kowalczyk, Magdalena Bartnik-Głaska, Marta Smyk, Izabela Plaskota, Joanna Bernaciak, Marta Kędzior, Barbara Wiśniowiecka-Kowalnik, Krystyna Jakubów-Durska, Natalia Braun-Walicka, Artur Barczyk, Maciej Geremek, Jennifer Castañeda, Anna Kutkowska-Kaźmierczak, Paweł Własienko, Marzena Debska, Anna Kucińska-Chahwan, Tomasz Roszkowski, Szymon Kozłowski, Boyana Mikulska, Tadeusz Issat, Ewa Obersztyn, Beata Anna Nowakowska
Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities. Genes 12 (12) (2021)
Marta Unolt, Molka Kammoun, Sebastian Kwiatkowski, Gail E Graham, Terrence Blaine Crowley, Matthew S Hestand, Wolfram Demaerel, Maciej Geremek, Beverly S Emanuel, Elaine H Zackai, Joris R Vermeesch, Donna M McDonald-McGinn
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition. Genetics in medicine : official journal of the American College of Medical Genetics 22 (2) (2019)
Maciej Geremek, Lech Dudarewicz, Ewa Obersztyn, Magdalena Paczkowska, Marta Smyk, Katarzyna Sobecka, Beata Nowakowska
Null variants in AGRN cause lethal fetal akinesia deformation sequence. Clinical genetics 97 (4) (2019)