Giedré Grigelioniené

3.3k total citations
57 papers, 1.3k citations indexed

About

Giedré Grigelioniené is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Giedré Grigelioniené has authored 57 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Genetics, 36 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Giedré Grigelioniené's work include Connective tissue disorders research (20 papers), Congenital heart defects research (7 papers) and Ubiquitin and proteasome pathways (6 papers). Giedré Grigelioniené is often cited by papers focused on Connective tissue disorders research (20 papers), Congenital heart defects research (7 papers) and Ubiquitin and proteasome pathways (6 papers). Giedré Grigelioniené collaborates with scholars based in Sweden, United States and Japan. Giedré Grigelioniené's co-authors include Eva Åström, Andreas Kindmark, B. Malmgren, Katarina Lindahl, Lars Hagenäs, Östen Ljunggren, Carl‐Johan Rubin, Gen Nishimura, Lars Sävendahl and J Wróblewski and has published in prestigious journals such as Nature Medicine, Nature Genetics and PLoS ONE.

In The Last Decade

Giedré Grigelioniené

54 papers receiving 1.2k citations

Peers

Countries citing papers authored by Giedré Grigelioniené

Since Specialization

Citations

This map shows the geographic impact of Giedré Grigelioniené's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Giedré Grigelioniené with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Giedré Grigelioniené more than expected).

Fields of papers citing papers by Giedré Grigelioniené

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Giedré Grigelioniené. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Giedré Grigelioniené. The network helps show where Giedré Grigelioniené may publish in the future.

Co-authorship network of co-authors of Giedré Grigelioniené

This figure shows the co-authorship network connecting the top 25 collaborators of Giedré Grigelioniené. A scholar is included among the top collaborators of Giedré Grigelioniené based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Giedré Grigelioniené. Giedré Grigelioniené is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genome sequencing in a cohort of 32 fetuses with genetic skeletal disorders 2025 ·European Journal of Human Genetics ·(unknown), Anna Hammarsjö, (unknown), (unknown), Peter Conner, Nikos Papadogiannakis, (unknown), Laura Orellana, Malin Kvarnung, Helena Malmgren, Kristina Lagerstedt‐Robinson, Ann Nordgren, Anna Lindstrand, Gen Nishimura, Giedré Grigelioniené	1
2	Genotypic and Phenotypic Characterization of Seven Individuals With Predicted Bone Morphogenetic Protein 2 ( BMP2 ) Haploinsufficiency 2025 ·Clinical Genetics ·(unknown), Anna Hammarsjö, Anna Lindstrand, Ann Nordgren, Giedré Grigelioniené, Maritta Hellström Pigg	0
3	Structural Variants in COL1A1 and COL1A2 in Osteogenesis Imperfecta 2024 ·American Journal of Medical Genetics Part A ·(unknown), Diana Swolin‐Eide, Anna Hammarsjö, (unknown), (unknown), (unknown), Jesper Eisfeldt, Anna Lindstrand, Ann Nordgren, Eva Åström, Giedré Grigelioniené	1
4	Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome 2023 ·Frontiers in Genetics ·(unknown), (unknown), Maria Pettersson, Dora Dias‐Santagata, Daniel Nilsson, Anna Hammarsjö, Anna Lindstrand, (unknown), Janey L. Wiggs, David S. Walton, Paula Goldenberg, Jesper Eisfeldt, Angela E. Lin, Ralph S. Lachman, Gen Nishimura, Giedré Grigelioniené	5
5	Skeletal Dysplasia Families: A Stepwise Approach to Diagnosis 2023 ·Radiographics ·Atsuhiko Handa, Giedré Grigelioniené, Gen Nishimura	11
6	Expanding the phenotype of Seckel syndrome associated with biallelic loss‐of‐function variants in CEP63 2023 ·American Journal of Medical Genetics Part A ·(unknown), Maria Pettersson, Anna Lindstrand, Giedré Grigelioniené	1
7	Compound heterozygous variants in RAB34 in a rare skeletal ciliopathy syndrome 2023 ·Clinical Genetics ·(unknown), (unknown), Anna Hammarsjö, Ritsuko K. Pooh, Osamu Shimokawa, Shiro Ikegawa, Giedré Grigelioniené, Gen Nishimura, Takahiro Yamada	2
8	A hypomorphic variant in the translocase of the outer mitochondrial membrane complex subunit TOMM7 causes short stature and developmental delay 2022 ·Human Genetics and Genomics Advances ·(unknown), (unknown), (unknown), Maria Shvedova, Yutaro Mihara, Jun Akiba, Wen Zhou, Anna Hammarsjö, Gen Nishimura, Shuichi Yatsuga, Giedré Grigelioniené, Tatsuya Kobayashi	12
9	Case Report: Inversion of LMX1B - A Novel Cause of Nail-Patella Syndrome in a Swedish Family and a Longtime Follow-Up 2022 ·Frontiers in Endocrinology ·(unknown), Eva Horemuzova, (unknown), Ann Nordgren, Giedré Grigelioniené, Anna Hammarsjö	1
10	Gain-of-function mutation of microRNA-140 in human skeletal dysplasia 2019 ·Nature Medicine ·Giedré Grigelioniené, Hiroshi Suzuki, Fulya Taylan, Fatemeh Mirzamohammadi, Zvi Borochowitz, Ugur M. Ayturk, Shay Tzur, Eva Horemuzova, Anna Lindstrand, Mary Ann Weis, (unknown), Anna Hammarsjö, Elin Marsk, Ann Nordgren, Magnus Nordenskjöld, David W. Eyre, Matthew L. Warman, Gen Nishimura, Phillip A. Sharp, Tatsuya Kobayashi	70
11	Alu-Alu mediated intragenic duplications in IFT81 and MATN3 are associated with skeletal dysplasias 2018 ·Human Mutation ·Maria Pettersson, Raquel Vaz, Anna Hammarsjö, Jesper Eisfeldt, Claudia M.B. Carvalho, Wolfgang Hofmeister, Emma Tham, Eva Horemuzova, (unknown), Gen Nishimura, (unknown), Ann Nordgren, Daniel Nilsson, Giedré Grigelioniené, Anna Lindstrand	11
12	Growth in achondroplasia: Development of height, weight, head circumference, and body mass index in a European cohort 2018 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Niels Thomas Hertel, Giedré Grigelioniené, Outi Mäkitie, Klaus Mohnike, Lars Hagenäs	49
13	Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta – A retrospective cohort study 2017 ·PLoS ONE ·(unknown), Göran Dahllöf, Katarina Lindahl, Andreas Kindmark, Giedré Grigelioniené, Eva Åström, B. Malmgren	63
14	Autosomal recessive brachyolmia: early radiological findings 2016 ·Skeletal Radiology ·Atsuhiko Handa, Emma Tham, Zheng Wang, Eva Horemuzova, Giedré Grigelioniené	4
15	Short Stature in KBG Syndrome: First Responses to Growth Hormone Treatment 2015 ·Hormone Research in Paediatrics ·(unknown), Charlotte W. Ockeloen, Lars Sävendahl, Dominique Beckers, Koenraad Devriendt, Tjitske Kleefstra, Carine Carels, Giedré Grigelioniené, Ann Nordgren, Inge François, Francis de Zegher, Kristina Casteels	24
16	Extending the phenotype of lethal skeletal dysplasia type al Gazali 2011 ·American Journal of Medical Genetics Part A ·Giedré Grigelioniené, Nikos Papadogiannakis, Peter Conner, (unknown), Masanori Nishikawa, Masahiro Nakayama	0
17	Clinical and molecular characterization of duplications encompassing the human SHOX gene reveal a variable effect on stature 2009 ·American Journal of Medical Genetics Part A ·N. Simon Thomas, John F. Harvey, David J. Bunyan, Julia Rankin, Giedré Grigelioniené, Damien L. Bruno, Tiong Yang Tan, Susan Tomkins, Robert Hastings	43
18	Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus 2007 ·BMC Genomics ·(unknown), Patrick G. Buckley, Giedré Grigelioniené, Arkadiusz Piotrowski, Anders R. Hellström, Kiran K. Mantripragada, (unknown), Tiit Mathiesen, Jan P. Dumanski	60
19	Analysis of short stature homeobox-containing gene ( SHOX ) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity 2001 ·Human Genetics ·Giedré Grigelioniené, Jacqueline Schoumans, (unknown), Sten A. Ivarsson, (unknown), (unknown), (unknown), (unknown), Anne Grethe Myhre, Otto Westphal, Nils Östen Nilsson, Maria Elfving, Ian O. Ellis, Britt‐Marie Anderlid, Ingegerd Fransson, Isabel Tapia‐Páez, Magnus Nordenskj�ld, (unknown), Jan P. Dumanski	38
20	Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia 2000 ·Human Genetics ·Giedré Grigelioniené, O. Eklöf, Sten A. Ivarsson, Otto Westphal, (unknown), Darek Kedra, Jan P. Dumanski, Lars Hagenäs	30

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