Ellika Sahlin

775 total citations
13 papers, 193 citations indexed

About

Ellika Sahlin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Ellika Sahlin has authored 13 papers receiving a total of 193 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 4 papers in Molecular Biology. Recurrent topics in Ellika Sahlin's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Ellika Sahlin is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Ellika Sahlin collaborates with scholars based in Sweden and United Kingdom. Ellika Sahlin's co-authors include Erik Iwarsson, Magnus Nordenskjöld, Peter Gustavsson, Agne Liedén, Nikos Papadogiannakis, Josephine Wincent, Susanne Georgsson, Malin Kvarnung, Elisabeth Syk Lundberg and Karin Pettersson and has published in prestigious journals such as PLoS ONE, Genomics and Ultrasound in Obstetrics and Gynecology.

In The Last Decade

Ellika Sahlin

13 papers receiving 188 citations

Peers

Countries citing papers authored by Ellika Sahlin

Since Specialization

Citations

This map shows the geographic impact of Ellika Sahlin'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 Ellika Sahlin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ellika Sahlin more than expected).

Fields of papers citing papers by Ellika Sahlin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ellika Sahlin. 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 Ellika Sahlin. The network helps show where Ellika Sahlin may publish in the future.

Co-authorship network of co-authors of Ellika Sahlin

This figure shows the co-authorship network connecting the top 25 collaborators of Ellika Sahlin. A scholar is included among the top collaborators of Ellika Sahlin 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 Ellika Sahlin. Ellika Sahlin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Whole‐genome sequencing in prenatally detected congenital malformations: prospective cohort study in clinical setting 2024 ·Ultrasound in Obstetrics and Gynecology ·(unknown), Peter Conner, Maria Pettersson, Ellika Sahlin, Nikos Papadogiannakis, Anna Lindstrand, Erik Iwarsson	5
2	Diagnostic yield using whole‐genome sequencing and in‐silico panel of 281 genes associated with non‐immune hydrops fetalis in clinical setting 2022 ·Ultrasound in Obstetrics and Gynecology ·(unknown), Ellika Sahlin, Peter Conner, Anna Lindstrand, Erik Iwarsson	7
3	Massive parallel sequencing in a family with rectal cancer 2021 ·Hereditary Cancer in Clinical Practice ·(unknown), Jessada Thutkawkorapin, Ellika Sahlin, Annika Lindblom, Kristina Lagerstedt‐Robinson	2
4	Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirth 2019 ·PLoS ONE ·Ellika Sahlin, Anna Gréen, Peter Gustavsson, Agne Liedén, Magnus Nordenskjöld, Nikos Papadogiannakis, Karin Pettersson, Daniel Nilsson, Jon Jonasson, Erik Iwarsson	19
5	Pathogenic copy number variants are detected in a subset of patients with gastrointestinal malformations 2019 ·Molecular Genetics & Genomic Medicine ·(unknown), Peter Gustavsson, Ellika Sahlin, Magnus Larsson, Henrik Ehrén, Magdalena Fossum, Tomas Wester, Ann Nordgren, Agneta Nordenskjöld	3
6	Positive Attitudes towards Non-Invasive Prenatal Testing (NIPT) in a Swedish Cohort of 1,003 Pregnant Women 2016 ·PLoS ONE ·Ellika Sahlin, Magnus Nordenskjöld, Peter Gustavsson, Josephine Wincent, Susanne Georgsson, Erik Iwarsson	32
7	Knowledge and Attitudes Regarding Non‐Invasive Prenatal Testing (NIPT) and Preferences for Risk Information among High School Students in Sweden 2016 ·Journal of Genetic Counseling ·Susanne Georgsson, Ellika Sahlin, (unknown), Magnus Nordenskjöld, Peter Gustavsson, Erik Iwarsson	9
8	Fetal Calcifications Are Associated with Chromosomal Abnormalities 2015 ·PLoS ONE ·Ellika Sahlin, (unknown), (unknown), Erik Iwarsson, Nikos Papadogiannakis	10
9	Rare copy number variants are common in young children with autism spectrum disorder 2015 ·Acta Paediatrica ·Mats Eriksson, Agne Liedén, Joakim Westerlund, Anna Bremer, Josephine Wincent, Ellika Sahlin, Christopher Gillberg, Elisabeth Fernell, Britt‐Marie Anderlid	16
10	Amplification-free sequencing of cell-free DNA for prenatal non-invasive diagnosis of chromosomal aberrations 2014 ·Genomics ·Kasper Karlsson, Ellika Sahlin, Erik Iwarsson, Magnus Westgren, Magnus Nordenskjöld, Sten Linnarsson	23
11	Mutation Screening and Array Comparative Genomic Hybridization Using a 180K Oligonucleotide Array in VACTERL Association 2014 ·PLoS ONE ·(unknown), Peter Gustavsson, Nikos Papadogiannakis, Ellika Sahlin, (unknown), (unknown), Pär‐Johan Svensson, Göran Annerén, Erik Iwarsson, Ann Nordgren, Agneta Nordenskjöld	17
12	Molecular and Cytogenetic Analysis in Stillbirth: Results from 481 Consecutive Cases 2014 ·Fetal Diagnosis and Therapy ·Ellika Sahlin, Peter Gustavsson, Agne Liedén, Nikos Papadogiannakis, (unknown), Karin Pettersson, Magnus Nordenskjöld, Erik Iwarsson	20
13	Intragenic duplication—A novel causative mechanism for SATB2‐associated syndrome 2014 ·American Journal of Medical Genetics Part A ·Agne Liedén, Malin Kvarnung, (unknown), Ellika Sahlin, Elisabeth Syk Lundberg	30

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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