Concepedia

Hannele Koillinen

HK

Statistics

Publications

14

Citations

904

H-Index

14

Active since

2001

Affiliations

University of Helsinki(Current)

Helsinki University Hospital

Karolinska Institutet

University of Turku

Turku University Hospital

Hannele Koillinen is an author at University of Helsinki specializing in molecular genetics, genetics, and life sciences.

Publications per year

2001–2023

14

Publications

14

Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development

Myriam Peyrard‐Janvid, Elizabeth J. Leslie, Youssef A. Kousa et al. · The American Journal of Human Genetics · 2013 · 230 citations · Full text

, , +17

Genetics and genotype–phenotype correlations in Finnish patients with dilated cardiomyopathy

Oyediran Akinrinade, Laura Ollila, Sanna Vattulainen et al. · European Heart Journal · 2015 · 166 citations · Full text

, , +13

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34

Hannele Koillinen, Fung Ki Wong, Jorma Rautio et al. · European Journal of Human Genetics · 2001 · 70 citations

, , +9

Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia

Miia Melkoniemi, Hannele Koillinen, Minna Männikkö et al. · European Journal of Human Genetics · 2003 · 69 citations · Full text

, , +16

Identification of novel candidate disease genes from de novo exonic copy number variants

Tomasz Gambin, Bo Yuan, Weimin Bi et al. · Genome Medicine · 2017 · 63 citations · Full text

, , +17

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