Most cited papers from Väestöliitto

Väestöliitto

What are the most cited papers from Väestöliitto?

The most cited paper from Väestöliitto is "Efficacy of human papillomavirus (HPV)-16/18 AS04-adjuvanted vaccine against cervical infection and precancer caused by oncogenic HPV types (PATRICIA): final analysis of a double-blind, randomised study in young women" (Jorma A. Paavonen et al., 2009), with 1,663 citations. Next come "Efficacy of a prophylactic adjuvanted bivalent L1 virus-like-particle vaccine against infection with human papillomavirus types 16 and 18 in young women: an interim analysis of a phase III double-blind, randomised controlled trial" (1,320) and "Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene" (1,213).

Published TypeFieldAccessCitations

Showing 50 of 60 papers. Every paper with more than 151 citations is listed.

Most cited papers, sortable by citations and release date
#	Paper
1	Efficacy of human papillomavirus (HPV)-16/18 AS04-adjuvanted vaccine against cervical infection and precancer caused by oncogenic HPV types (PATRICIA): final analysis of a double-blind, randomised study in young women Jorma A. Paavonen et al. · The Lancet	Jul 2009	1,663
2	Efficacy of a prophylactic adjuvanted bivalent L1 virus-like-particle vaccine against infection with human papillomavirus types 16 and 18 in young women: an interim analysis of a phase III double-blind, randomised controlled trial Jorma A. Paavonen et al. · The Lancet	Jun 2007	1,320
3	Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene Renee A. Reijo Pera, Tien-Yi Lee, Pia Salo et al. · Nature Genetics	Aug 1995	1,213
4	Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease Lauri A. Aaltonen, Reijo Salovaara, Paula Kristo et al. · New England Journal of Medicine Open access	21 May 1998	1,169
5	Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting Claus Højbjerg Gravholt, N.H. Andersen, Gerard Conway et al. · European Journal of Endocrinology Open access	13 Jul 2017	1,119
6	Why do singletons conceived after assisted reproduction technology have adverse perinatal outcome? Systematic review and meta-analysis Anja Bisgaard Pinborg, Ulla‐Britt Wennerholm, Liv Bente Romundstad et al. · Human Reproduction Update Review	14 Nov 2012	715
7	Overall efficacy of HPV-16/18 AS04-adjuvanted vaccine against grade 3 or greater cervical intraepithelial neoplasia: 4-year end-of-study analysis of the randomised, double-blind PATRICIA trial Matti Lehtinen et al. · The Lancet Oncology	9 Nov 2011	708
8	Mutations in AXIN2 Cause Familial Tooth Agenesis and Predispose to Colorectal Cancer Laura Lammi, Sirpa Arte, Mirja Somer et al. · The American Journal of Human Genetics Open access	16 Apr 2004	695
9	Low dose mifepristone and two regimens of levonorgestrel for emergency contraception: a WHO multicentre randomised trial Helena von Hertzen, Gilda GP Piaggio, Alexandre Peregoudov et al. · The Lancet	Dec 2002	575
10	Mutations in the Gene Encoding Cystatin B in Progressive Myoclonus Epilepsy (EPM1) Len A. Pennacchio, Anna‐Elina Lehesjoki, Nancy Stone et al. · Science	22 Mar 1996	542
11	Cross-protective efficacy of HPV-16/18 AS04-adjuvanted vaccine against cervical infection and precancer caused by non-vaccine oncogenic HPV types: 4-year end-of-study analysis of the randomised, double-blind PATRICIA trial Cosette Marie Wheeler et al. · The Lancet Oncology	9 Nov 2011	515
12	Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport Juha Kolehmainen, Graeme Charles M. Black, Anne Saarinen et al. · The American Journal of Human Genetics Open access	Jun 2003	385
13	A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1 Richard Crook, Auli Verkkoniemi, Jordi Pérez‐Tur et al. · Nature Medicine	Apr 1998	353
14	The Axon Guidance Receptor Gene ROBO1 Is a Candidate Gene for Developmental Dyslexia Katariina Hannula‐Jouppi, Nina Kaminen‐Ahola, Mikko Taipale et al. · PLoS Genetics Open access	26 Oct 2005	336
15	Genomic Variation and Gene Conversion in Spinal Muscular Atrophy: Implications for Disease Process and Clinical Phenotype Louise J. Campbell, Allyson C. Potter, Jaakko Ignatius et al. · The American Journal of Human Genetics Open access	Jul 1997	325
16	Haploinsufficiency of TCF4 Causes Syndromal Mental Retardation with Intermittent Hyperventilation (Pitt-Hopkins Syndrome) Christiane Zweier, Maarit M. Peippo, Juliane Hoyer et al. · The American Journal of Human Genetics Open access	11 Apr 2007	324
17	Perinatal outcome of children born after frozen and fresh embryo transfer: the Finnish cohort study 1995–2006 Sari Pelkonen, Riku-Jaakko Koivunen, Mika Gissler et al. · Human Reproduction	2 Feb 2010	315
18	Mutations in the tyrosine phosphatase CD45 gene in a child with severe combined immunodeficiency disease Chun Kung, Jeanette T. Pingel, Markku Heikinheimo et al. · Nature Medicine	Mar 2000	314
19	Children born after cryopreservation of embryos or oocytes: a systematic review of outcome data Ulla‐Britt Wennerholm, Viveca Söderström‐Anttila, Christina Bergh et al. · Human Reproduction Review	20 May 2009	306
20	Elective transfer of one embryo results in an acceptable pregnancy rate and eliminates the risk of multiple birth Sirpa Vilska, Aila E. Tiitinen, Christel Hydén‐Granskog et al. · Human Reproduction	Sep 1999	304
21	Extracellular matrix improves survival of both stored and fresh human primordial and primary ovarian follicles in long-term culture Outi Hovatta, René Silye, Ronit Abir et al. · Human Reproduction Open access	May 1997	298
22	Epidemiology of HPV 16 and Cervical Cancer in Finland and the Potential Impact of Vaccination: Mathematical Modelling Analyses Ruanne V. Barnabas, Päivi Laukkanen, Pentti U. Koskela et al. · PLoS Medicine Open access	30 Mar 2006	296
23	De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome Alexander Hoischen et al. · Nature Genetics	26 Jun 2011	281
24	Human Growth Differentiation Factor 9 (GDF-9) and Its Novel Homolog GDF-9B Are Expressed in Oocytes during Early Folliculogenesis1 Johanna Aaltonen, Mika Laitinen, Kaisa Vuojolainen et al. · The Journal of Clinical Endocrinology & Metabolism	Aug 1999	274
25	Effects of Oral and Transdermal Estrogen Replacement Therapy on Markers of Coagulation, Fibrinolysis, Inflammation and Serum Lipids and Lipoproteins in Postmenopausal Women Satu Vehkavaara, Angela Maria Vidigal Silveira, Tiina Hakala‐Ala‐Pietilä et al. · Thrombosis and Haemostasis	2001	271
26	Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes Susanna Annunen et al. · The American Journal of Human Genetics Open access	Oct 1999	265
27	Intrauterine insemination treatment in subfertility: an analysis of factors affecting outcome S. Nuojua-Huttunen · Human Reproduction	Mar 1999	262
28	MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome Mira Kyttälä, Jonna Tallila, Riitta Salonen et al. · Nature Genetics	15 Jan 2006	257
29	Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1 Angela E. Lin, Patricia H. Birch, Bruce R. Korf et al. · American Journal of Medical Genetics	2000	243
30	The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperone Anna‐Kaisa Anttonen, Ibrahim Mahjneh, Riikka H. Hämäläinen et al. · Nature Genetics	10 Nov 2005	242
31	A Transcript Map of the Newly Defined 165 kb Wolf-Hirschhorn Syndrome Critical Region Tracy J. Wright, Darrell O. Ricke, Karen Denison et al. · Human Molecular Genetics Open access	Feb 1997	236
32	Physical attractiveness and reproductive success in humans: evidence from the late 20th century United States Markus M. Jokela · Evolution and Human Behavior Open access	10 May 2009	236
33	Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation Guy Froyen et al. · The American Journal of Human Genetics Open access	28 Jan 2008	227
34	Cardiovascular manifestations in 75 patients with Williams syndrome Marianne P. Eronen, M Peippo, A Hiippala et al. · Journal of Medical Genetics Open access	Aug 2002	226
35	Natural History of Progression of HPV Infection to Cervical Lesion or Clearance: Analysis of the Control Arm of the Large, Randomised PATRICIA Study Unnop Jaisamrarn et al. · PLoS ONE Open access	19 Nov 2013	218
36	N-Glycolylneuraminic Acid Xenoantigen Contamination of Human Embryonic and Mesenchymal Stem Cells Is Substantially Reversible Annamari Heiskanen, Tero Satomaa, Sari L. Tiitinen et al. · Stem Cells Open access	28 Sep 2006	215
37	Surrogacy: outcomes for surrogate mothers, children and the resulting families—a systematic review Viveca Söderström‐Anttila, Ulla‐Britt Wennerholm, Anne Loft et al. · Human Reproduction Update ReviewOpen access	9 Oct 2015	213
38	Finnish Disease Heritage I: Reijo Norio · Human Genetics	8 Mar 2003	211
39	Klinefelter Syndrome in Adolescence: Onset of Puberty Is Associated with Accelerated Germ Cell Depletion Anne M. Wikström, Taneli Raivio, F. Hadžiselimović et al. · The Journal of Clinical Endocrinology & Metabolism	May 2004	207
40	The Meckel syndrome: Clinicopathological findings in 67 patients Riitta Salonen, John M. Opitz, James F. Reynolds · American Journal of Medical Genetics	Aug 1984	205
41	De novoSCN1Amutations are a major cause of severe myoclonic epilepsy of infancy Lieve R. F. Claes, Berten Ceulemans, Dominique Audenaert et al. · Human Mutation Open access	22 Apr 2003	204
42	Citalopram and fluoxetine in the treatment of postmenopausal symptoms: a prospective, randomized, 9-month, placebo-controlled, double-blind study Eila Suvanto‐Luukkonen, Riitta M. Koivunen, Helena Sundstr m et al. · Menopause The Journal of The North American Menopause Society	2005	203
43	A randomized, phase II study describing the efficacy, bleeding profile, and safety of two low-dose levonorgestrel-releasing intrauterine contraceptive systems and Mirena Kristina Gemzell‐Danielsson, Ilka Schellschmidt, Dan Apter · Fertility and Sterility Open access	4 Jan 2012	201
44	PROGRESSIVE MYOCLONUS EPILEPSY Marjaleena Koskiniemi, M. Donner, H. Majuri et al. · Acta Neurologica Scandinavica	29 Jan 2009	197
45	Pregnancy outcome of women exposed to azathioprine during pregnancy Lee Hilary Goldstein, Galit Dolinsky, Revital Greenberg et al. · Birth Defects Research Part A Clinical and Molecular Teratology	10 Sep 2007	194
46	Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1 Kimmo I. Virtaneva, Elena D’Amato, Jinmin Miao et al. · Nature Genetics	Apr 1997	191
47	Early cleavage predicts the viability of human embryos in elective single embryo transfer procedures Andres Salumets · Human Reproduction	27 Mar 2003	188
48	Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q Eeva‐Marja Sankila, Leenamaija Pakarinen, Helena A. Kääriäinen et al. · Human Molecular Genetics	1995	187
49	Turner's syndrome and pregnancies after oocyte donation Tuija Foudila, Viveca Söderström‐Anttila, Outi Hovatta · Human Reproduction	Feb 1999	186
50	High and low BMI increase the risk of miscarriage after IVF/ICSI and FET Zdravka Veleva, A. Tiitinen, Sirpa Vilska et al. · Human Reproduction	31 Jan 2008	185

Citations are OpenAlex's own counts, from its 2026-09-23 snapshot, so the ranking can differ from Google Scholar or Web of Science. A paper is listed for an institution when any of its authors gave it as an affiliation; retracted papers and papers whose citation count cannot be traced to citing works are left out, and a preprint and the article it became are shown once. Release dates are OpenAlex's: where a source gave only a month or a year, that is what is shown. How the lists are chosen.