Personal information

Other IDs

Loop profile: 562722
Scopus Author ID: 56784386200
Scopus Author ID: 57203005023

Keywords

Genomic disorders; Hereditary kidney disease; Clinical genetics

Countries

Poland

Activities

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Employment (1)

Medical University of Gdansk: Gdańsk, PL

2015-12-03 to present | Associate Professor (Department of Biology and Medical Genetics, Clinical Genetics Unit)
Employment
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz

Professional activities (3)

Interational Pediatric Nephrology Association: Prague, CZ

2020-01-01 to present
Membership
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz

European Society for Paediatric Nephrology: Essen, DE

2020-01-01 to present | regular member
Membership
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz

Polish Society of Human Genetics: Bydgoszcz, PL

2010-09 to present
Membership
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz

Works (50 of 60)

Items per page:
Page 1 of 2

Genetic testing in the diagnosis of chronic kidney disease: Recommendations for clinical practice

Nephrology Dialysis Transplantation
2022 | Journal article
DOI: 10.1093/ndt/gfab218
EID:

2-s2.0-85127302685

Part of ISSN: 14602385 09310509
Contributors: Knoers, N.; Antignac, C.; Bergmann, C.; Dahan, K.; Giglio, S.; Heidet, L.; Lipska-Ziȩtkiewicz, B.S.; Noris, M.; Remuzzi, G.; Vargas-Poussou, R. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Genotype–phenotype correlations for COL4A3–COL4A5 variants resulting in Gly substitutions in Alport syndrome

Scientific Reports
2022 | Journal article
DOI: 10.1038/s41598-022-06525-9
EID:

2-s2.0-85124777121

Part of ISSN: 20452322
Contributors: Gibson, J.T.; Huang, M.; Shenelli Croos Dabrera, M.; Shukla, K.; Rothe, H.; Hilbert, P.; Deltas, C.; Storey, H.; Lipska-Ziętkiewicz, B.S.; Chan, M.M.Y. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Guidelines for Genetic Testing and Management of Alport Syndrome

Clinical Journal of the American Society of Nephrology
2022 | Journal article
DOI: 10.2215/CJN.04230321
EID:

2-s2.0-85123287024

Part of ISSN: 1555905X 15559041
Contributors: Savige, J.; Lipska-Zietkiewicz, B.S.; Watson, E.; Hertz, J.M.; Deltas, C.; Mari, F.; Hilbert, P.; Plevova, P.; Byers, P.; Cerkauskaite, A. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Later Response to Corticosteroids in Adults With Primary Focal Segmental Glomerular Sclerosis Is Associated With Favorable Outcomes

Kidney International Reports
2022 | Journal article
DOI: 10.1016/j.ekir.2021.10.016
EID:

2-s2.0-85119654214

Part of ISSN: 24680249
Contributors: Rood, I.M.; Bavinck, A.; Lipska-Ziętkiewicz, B.S.; Lugtenberg, D.; Schaefer, F.; Deegens, J.K.J.; Wetzels, J.F.M.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Multicenter study on the genetics of glomerular diseases among southeast and south Asians: Deciphering Diversities - Renal Asian Genetics Network (DRAGoN)

Clinical Genetics
2022 | Journal article
DOI: 10.1111/cge.14116
EID:

2-s2.0-85124743211

Part of ISSN: 13990004 00099163
Contributors: Lu, L.; Yap, Y.-C.; Nguyen, D.Q.; Chan, Y.-H.; Ng, J.-L.; Zhang, Y.-C.; Chan, C.-Y.; Than, M.; Liu, I.D.; Asim, S. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.

Kidney international
2022-04-26 | Journal article
DOI: 10.1016/j.kint.2022.02.040
PMID: 35483523
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz

Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.

Kidney international
2022-04-20 | Journal article
DOI: 10.1016/j.kint.2022.03.019
PMID: 35460632
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz

The 2019 and 2021 International Workshops on Alport Syndrome.

European journal of human genetics : EJHG
2022-03-09 | Journal article
DOI: 10.1038/s41431-022-01075-0
PMID: 35260866
PMC: PMC8904161
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz
grade
Preferred source (of 2)‎

Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

European Journal of Human Genetics
2021 | Journal article
DOI: 10.1038/s41431-021-00858-1
EID:

2-s2.0-85104672127

Part of ISSN: 14765438 10184813
Contributors: Savige, J.; Storey, H.; Watson, E.; Hertz, J.M.; Deltas, C.; Renieri, A.; Mari, F.; Hilbert, P.; Plevova, P.; Byers, P. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Five-Year Follow-Up and Successful Kidney Transplantation in a Girl with a Severe Phenotype of Pierson Syndrome

Nephron
2021 | Journal article
DOI: 10.1159/000516247
EID:

2-s2.0-85107683695

Part of ISSN: 22353186 16608151
Contributors: Sobieszczańska-Droździel, A.; Grenda, R.; Lipska-Ziȩtkiewicz, B.S.; Korolczuk, A.; Jarmużek, W.; Sikora, P.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Genetic Basis of Nephrotic Syndrome

Pediatric Nephrology
2021 | Book chapter
DOI: 10.1007/978-3-642-27843-3_90-1
Part of ISBN: 9783642278433
Part of ISBN: 9783642278433
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz

Immune Dysregulation in Patients With Chromosome 18q Deletions—Searching for Putative Loci for Autoimmunity and Immunodeficiency

Frontiers in Immunology
2021 | Journal article
DOI: 10.3389/fimmu.2021.742834
EID:

2-s2.0-85120490562

Part of ISSN: 16643224
Contributors: Hogendorf, A.; Zieliński, M.; Constantinou, M.; Śmigiel, R.; Wierzba, J.; Wyka, K.; Wędrychowicz, A.; Jakubiuk-Tomaszuk, A.; Budzynska, E.; Piotrowicz, M. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group

Nature Reviews Nephrology
2021 | Journal article
DOI: 10.1038/s41581-020-00384-1
EID:

2-s2.0-85099979604

Part of ISSN: 1759507X 17595061
Contributors: Boyer, O.; Schaefer, F.; Haffner, D.; Bockenhauer, D.; Hölttä, T.; Bérody, S.; Webb, H.; Heselden, M.; Lipska-Zie˛tkiewicz, B.S.; Ozaltin, F. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlife

Kidney International
2021 | Journal article
DOI: 10.1016/j.kint.2020.10.040
EID:

2-s2.0-85102116996

Part of ISSN: 15231755 00852538
Contributors: Żurowska, A.M.; Bielska, O.; Daca-Roszak, P.; Jankowski, M.; Szczepańska, M.; Roszkowska-Bjanid, D.; Kuźma-Mroczkowska, E.; Pańczyk-Tomaszewska, M.; Moczulska, A.; Drożdż, D. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Non-syndromic inherited retinal diseases in Poland: Genes, mutations, and phenotypes

Molecular vision
2021 | Journal article
EID:

2-s2.0-85112696508

Part of ISSN: 10900535
Contributors: Tracewska, A.M.; Kocyła-Karczmarewicz, B.; Rafalska, A.; Murawska, J.; Jakubaszko-Jabłónska, J.; Rydzanicz, M.; Stawiński, P.; Ciara, E.; Lipska-Ziętkiewicz, B.S.; Khan, M.I. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Publisher Correction: Management of congenital nephrotic syndrome: consensus recommendations of the ERKNet-ESPN Working Group (Nature Reviews Nephrology, (2021), 17, 4, (277-289), 10.1038/s41581-020-00384-1)

Nature Reviews Nephrology
2021 | Journal article
DOI: 10.1038/s41581-021-00431-5
EID:

2-s2.0-85105140768

Part of ISSN: 1759507X 17595061
Contributors: Boyer, O.; Schaefer, F.; Haffner, D.; Bockenhauer, D.; Hölttä, T.; Bérody, S.; Webb, H.; Heselden, M.; Lipska-Ziętkiewicz, B.S.; Ozaltin, F. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Wide fontanels, delayed speech development and hoarse voice as useful signs in the diagnosis of kbg syndrome: A clinical description of 23 cases with pathogenic variants involving the ankrd11 gene or submicroscopic chromosomal rearrangements of 16q24.3

Genes
2021 | Journal article
DOI: 10.3390/genes12081257
EID:

2-s2.0-85113293086

Part of ISSN: 20734425
Contributors: Kutkowska‐kaźmierczak, A.; Boczar, M.; Kalka, E.; Castañeda, J.; Klapecki, J.; Pietrzyk, A.; Barczyk, A.; Malinowska, O.; Landowska, A.; Gambin, T. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Bilateral Ovarian Germ Cell Tumor in a 46,XX Female with Nijmegen Breakage Syndrome and hypergonadotropic hypogonadism.

Journal of clinical research in pediatric endocrinology
2021-09-21 | Journal article
DOI: 10.4274/jcrpe.galenos.2021.2021.0151
PMID: 34544220
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz

Dysgerminoma with a Somatic Exon 17 <i>KIT</i> Mutation and SHH Pathway Activation in a Girl with Turner Syndrome

Diagnostics
2020-12 | Journal article | Author
DOI: 10.3390/diagnostics10121067
Contributors: Ada Gawrychowska; ewa izycka-swieszewska; Beata S. Lipska-Ziętkiewicz; Dominika Kuleszo; Joanna Bautembach-Minkowska; Marcin Łosin; Joanna Stefanowicz
Source: check_circle
Multidisciplinary Digital Publishing Institute
grade
Preferred source (of 2)‎

Broad phenotypic spectrum of germline 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia

Genes, Chromosomes and Cancer
2020-11-02 | Journal article
DOI: 10.1002/gcc.22914
Part of ISSN: 1045-2257
Part of ISSN: 1098-2264
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz
grade
Preferred source (of 2)‎

Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet–ESPN inherited glomerulopathy working group

European Journal of Human Genetics
2020-05-28 | Journal article
DOI: 10.1038/s41431-020-0642-8
Part of ISSN: 1018-4813
Part of ISSN: 1476-5438
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz
grade
Preferred source (of 2)‎

WT1 Disorder

GeneReviews
2020-04-30 | Book chapter
PMID: 32352694
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz

Hedgehog signalling network gene status analysis in paediatric intracranial germ cell tumours

Folia Neuropathologica
2019 | Journal article
DOI: 10.5114/fn.2019.88451
Part of ISSN: 1641-4640
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz
grade
Preferred source (of 2)‎

NUP Nephropathy: When Defective Pores Cause Leaky Glomeruli

American Journal of Kidney Diseases
2019 | Journal article
DOI: 10.1053/j.ajkd.2019.01.015
EID:

2-s2.0-85062633672
Contributors: Lipska-Ziętkiewicz, B.S.; Schaefer, F.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

CoQ10-related sustained remission of proteinuria in a child with COQ6 glomerulopathy—a case report

Pediatric Nephrology
2018 | Journal article
DOI: 10.1007/s00467-018-4083-3
EID:

2-s2.0-85053543344
Contributors: Stańczyk, M.; Bałasz-Chmielewska, I.; Lipska-Ziętkiewicz, B.; Tkaczyk, M.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Exploring the clinical and genetic spectrum of steroid resistant nephrotic syndrome: The podonet registry

Frontiers in Pediatrics
2018 | Journal article
DOI: 10.3389/fped.2018.00200
EID:

2-s2.0-85052903011
Contributors: Trautmann, A.; Lipska-Ziȩtkiewicz, B.S.; Schaefer, F.; Csaicsich, D.; Azocar, M.; Quiroz, L.; Higuita, L.M.S.; Dušek, J.; Ranchin, B.; Fischbach, M. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Application of high-resolution genomic profiling in the differential diagnosis of liposarcoma

Molecular Cytogenetics
2017 | Journal article
DOI: 10.1186/s13039-017-0309-5
EID:

2-s2.0-85015215655
Contributors: Koczkowska, M.; Lipska-Ziętkiewicz, B.S.; Iliszko, M.; Ryś, J.; Miettinen, M.; Lasota, J.; Biernat, W.; Harazin-Lechowska, A.; Kruczak, A.; Limon, J.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Comparative genomic analysis of intracranial germ cell tumors – the preliminary study focused on Sonic Hedgehog signaling pathway

Współczesna Onkologia
2017 | Journal article
DOI: 10.5114/wo.2017.72390
Part of ISSN: 1428-2526
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz
grade
Preferred source (of 2)‎

Dent disease in Poland: what we have learned so far?

International Urology and Nephrology
2017 | Journal article
DOI: 10.1007/s11255-017-1676-x
EID:

2-s2.0-85027513378
Contributors: Zaniew, M.; Mizerska-Wasiak, M.; Załuska-Leśniewska, I.; Adamczyk, P.; Kiliś-Pstrusińska, K.; Haliński, A.; Zawadzki, J.; Lipska-Ziętkiewicz, B.S.; Pawlaczyk, K.; Sikora, P. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome

Journal of Applied Genetics
2017 | Journal article
DOI: 10.1007/s13353-016-0366-1
EID:

2-s2.0-84987623855
Contributors: Koczkowska, M.; Wierzba, J.; Śmigiel, R.; Sąsiadek, M.; Cabała, M.; Ślężak, R.; Iliszko, M.; Kardaś, I.; Limon, J.; Lipska-Ziętkiewicz, B.S.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Karyotype analysis in 5 210 individuals with a history of reproductive failure,Analiza KariotypÓw 5 210 pacjentÓw z wywiadem obci??onym niepowodzeniami rozrodu

Annales Academiae Medicae Gedanensis
2017 | Journal article
EID:

2-s2.0-85050181846

Part of ISSN: 03034135
Contributors: Gintowt-Chakour, A.; Sza?ecka, K.; Ku?niacka, A.; Zukowska, H.; Kuziemska, E.; Zdzitowiecka, M.; Karda?, I.; Iliszko, M.; Limon, J.; Lipska-Zi?tkiewicz, B.S.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Long-term outcome of steroid-resistant nephrotic syndrome in children

Journal of the American Society of Nephrology
2017 | Journal article
DOI: 10.1681/ASN.2016101121
EID:

2-s2.0-85030457670
Contributors: Trautmann, A.; Schnaidt, S.; Lipska-Ziȩtkiewicz, B.S.; Bodria, M.; Ozaltin, F.; Emma, F.; Anarat, A.; Melk, A.; Azocar, M.; Oh, J. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia

PLoS ONE
2017 | Journal article
DOI: 10.1371/journal.pone.0180926
EID:

2-s2.0-85027219757
Contributors: Lipska-Ziętkiewicz, B.S.; Gellermann, J.; Boyer, O.; Gribouval, O.; Ziętkiewicz, S.; Kari, J.A.; Shalaby, M.A.; Ozaltin, F.; Dusek, J.; Melk, A. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS

Journal of the American Society of Nephrology
2016 | Journal article
DOI: 10.1681/ASN.2014121240
EID:

2-s2.0-84954451992
Contributors: Korkmaz, E.; Lipska-Ziętkiewicz, B.S.; Boyer, O.; Gribouval, O.; Fourrage, C.; Tabatabaei, M.; Schnaidt, S.; Gucer, S.; Kaymaz, F.; Arici, M. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Chromosome 18q deletion syndrome with autoimmune diabetes mellitus: Putative genomic loci for autoimmunity and immunodeficiency

Pediatric Diabetes
2016 | Journal article
DOI: 10.1111/pedi.12235
EID:

2-s2.0-84970925808
Contributors: Hogendorf, A.; Lipska-Zietkiewicz, B.S.; Szadkowska, A.; Borowiec, M.; Koczkowska, M.; Trzonkowski, P.; Drozdz, I.; Wyka, K.; Limon, J.; Mlynarski, W.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Co-incidence of Turner syndrome and Duchenne muscular dystrophy - an important problem for the clinician

Developmental period medicine
2016 | Journal article
EID:

2-s2.0-85028594764
Contributors: Kaczorowska, E.; Zimowski, J.; Cichoń-Kotek, M.; Mrozińska, A.; Purzycka, J.; Wierzba, J.; Limon, J.; Lipska-Ziętkiewicz, B.S.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Erratum: Glomerulopathy in patients with distal duplication of chromosome 6p (BMC Nephrology (2016) 17 (43))

BMC Nephrology
2016 | Journal article
DOI: 10.1186/s12882-016-0255-1
EID:

2-s2.0-84969612599
Contributors: Jankauskiene, A.; Koczkowska, M.; Bjerre, A.; Bernaciak, J.; Schaefer, F.; Lipska-Zietkiewicz, B.S.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Glomerulopathy in patients with distal duplication of chromosome 6p

BMC Nephrology
2016 | Journal article
DOI: 10.1186/s12882-016-0246-2
EID:

2-s2.0-84963975958
Contributors: Jankauskiene, A.; Koczkowska, M.; Bjerre, A.; Bernaciak, J.; Schaefer, F.; Lipska-Ziȩtkiewicz, B.S.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

The algorithm for Alzheimer risk assessment based on APOE promoter polymorphisms

Alzheimer's Research and Therapy
2016 | Journal article
DOI: 10.1186/s13195-016-0187-9
EID:

2-s2.0-84971299225
Contributors: Limon-Sztencel, A.; Lipska-Ziȩtkiewicz, B.S.; Chmara, M.; Wasag, B.; Bidzan, L.; Godlewska, B.R.; Limon, J.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.

Clinical journal of the American Society of Nephrology : CJASN
2015-01 | Journal article
DOI: 10.2215/cjn.06260614
PMID: 25635037
PMC: PMC4386250
Contributors: Trautmann A; Bodria M; Ozaltin F; Gheisari A; Melk A; Azocar M; Anarat A; Caliskan S; Emma F; Gellermann J et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Europe PubMed Central
grade
Preferred source (of 2)‎

Genotype-phenotype associations in WT1 glomerulopathy

Kidney International
2014 | Journal article
DOI: 10.1038/ki.2013.519
EID:

2-s2.0-84899907617
Contributors: Lipska, B.S.; Ranchin, B.; Iatropoulos, P.; Gellermann, J.; Melk, A.; Ozaltin, F.; Caridi, G.; Seeman, T.; Tory, K.; Jankauskiene, A. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Mild phenotype of a large partial 13q trisomy

Clinical Dysmorphology
2014 | Journal article
DOI: 10.1097/MCD.0000000000000052
EID:

2-s2.0-84906838033
Contributors: Krygier, M.; Lipska-Zietkiewicz, B.S.; Koczkowska, M.; Wierzba, J.; Limon, J.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

NPHS2 mutations in steroid-resistant nephrotic syndrome: A mutation update and the associated phenotypic spectrum

Human Mutation
2014 | Journal article
DOI: 10.1002/humu.22485
EID:

2-s2.0-84891958291
Contributors: Bouchireb, K.; Boyer, O.; Gribouval, O.; Nevo, F.; Huynh-Cong, E.; Morinière, V.; Campait, R.; Ars, E.; Brackman, D.; Dantal, J. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Proliferation index revisited in neuroblastic tumors

Folia Neuropathologica
2014 | Journal article
DOI: 10.5114/fn.2014.45565
EID:

2-s2.0-84929615933
Contributors: Izycka-͆wieszewska, E.; Stefania Lipska-Ziętkiewicz, B.; Adamkiewicz-Drozyńska, E.; Grajkowska, W.; Hermann, B.; Bień, E.; Limon, J.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Erratum to: Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome (J Appl Genet., (2012), 10.1007/s13353-012-0126-9)

Journal of Applied Genetics
2013 | Journal article
DOI: 10.1007/s13353-013-0138-0
EID:

2-s2.0-84876057563
Contributors: Kuzniacka, A.; Wierzba, J.; Ratajska, M.; Lipska, B.S.; Koczkowska, M.; Malinowska, M.; Limon, J.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Genetic screening in adolescents with steroid-resistant nephrotic syndrome

Kidney International
2013 | Journal article
DOI: 10.1038/ki.2013.93
EID:

2-s2.0-84879689746
Contributors: Lipska, B.S.; Iatropoulos, P.; Maranta, R.; Caridi, G.; Ozaltin, F.; Anarat, A.; Balat, A.; Gellermann, J.; Trautmann, A.; Erdogan, O. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome

Pediatric Nephrology
2013 | Journal article
DOI: 10.1007/s00467-012-2379-2
EID:

2-s2.0-84880572908
Contributors: Kerti, A.; Csohány, R.; Szabó, A.; Árkossy, O.; Sallay, P.; Moriniére, V.; Vega-Warner, V.; Nyíro, G.; Lakatos, O.; Szabó, T. et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

On the significance of germline cytogenetic rearrangements at MYCN locus in neuroblastoma

Molecular Cytogenetics
2013 | Journal article
DOI: 10.1186/1755-8166-6-43
EID:

2-s2.0-84885444887
Contributors: Lipska, B.S.; Koczkowska, M.; Wierzba, J.; Ploszynska, A.; Iliszko, M.; Izycka-Swieszewska, E.; Adamkiewicz-Drozynska, E.; Limon, J.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Primary leiomyosarcoma of the mesentery in two sisters: Clinical and molecular characteristics

Polish Journal of Pathology
2013 | Journal article
DOI: 10.5114/PJP.2013.34605
EID:

2-s2.0-84876972704
Contributors: Koczkowska, M.; Lipska, B.S.; Grzeszewska, J.; Limon, J.; Biernat, W.; Jassem, J.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Scopus - Elsevier

Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population.

Journal of applied genetics
2013-05 | Journal article
DOI: 10.1007/s13353-013-0147-z
PMID: 23645318
PMC: PMC3721000
Contributors: Lipska BS; Balasz-Chmielewska I; Morzuch L; Wasielewski K; Vetter D; Borzecka H; Drozdz D; Firszt-Adamczyk A; Gacka E; Jarmolinski T et al.
Source: Self-asserted source
Beata S. Lipska-Ziętkiewicz via Europe PubMed Central
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Peer review (98 reviews for 24 publications/grants)

Review activity for American journal of kidney diseases : (1)
Review activity for American journal of medical genetics. (1)
Review activity for Annals of human genetics. (3)
Review activity for BMC medical genetics (7)
Review activity for BMC nephrology (6)
Review activity for Clinical case reports. (1)
Review activity for Clinical genetics (3)
Review activity for Clinical journal of the American Society of Nephrology. (3)
Review activity for Clinical kidney journal. (1)
Review activity for European journal of human genetics (2)
Review activity for F1000Research. (2)
Review activity for Human genomics (1)
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Review activity for Journal of the American Society of Nephrology : (1)
Review activity for Kidney international reports. (5)
Review activity for Molecular genetics and genomics. (1)
Review activity for Molecular genetics and genomics. (2)
Review activity for Nephrology, dialysis, transplantation. (9)
Review activity for Nephron journals. (18)
Review activity for Pediatric blood & cancer. (1)
Review activity for Pediatric nephrology. (2)
Review activity for Pediatric nephrology. (23)
Review activity for Pediatric research. (1)
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