Lea Puhakka

762 total citations
10 papers, 589 citations indexed

About

Lea Puhakka is a scholar working on Genetics, Physiology and Molecular Biology. According to data from OpenAlex, Lea Puhakka has authored 10 papers receiving a total of 589 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Physiology and 3 papers in Molecular Biology. Recurrent topics in Lea Puhakka's work include Lysosomal Storage Disorders Research (4 papers), Connective tissue disorders research (3 papers) and Carbohydrate Chemistry and Synthesis (2 papers). Lea Puhakka is often cited by papers focused on Lysosomal Storage Disorders Research (4 papers), Connective tissue disorders research (3 papers) and Carbohydrate Chemistry and Synthesis (2 papers). Lea Puhakka collaborates with scholars based in Finland, United States and Netherlands. Lea Puhakka's co-authors include Leena Peltonen, Katariina Kainulainen, Lynn Y. Sakai, Leena Karttunen, Aarno Palotie, Pirkko Santavuori, Irma Järvelä, A. H. Child, Rebecca M. Davidson and Lasse Ryhänen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Fertility and Sterility.

In The Last Decade

Lea Puhakka

10 papers receiving 575 citations

Peers

Countries citing papers authored by Lea Puhakka

Since Specialization

Citations

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

Fields of papers citing papers by Lea Puhakka

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lea Puhakka

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

#	Work	Indexed citations
1	Circulating antimüllerian hormone levels in boys decline during early puberty and correlate with inhibin B 2012 ·Fertility and Sterility ·Matti Hero, Johanna Tommiska, Kirsi Vaaralahti, Eeva‐Maria Laitinen, Ilkka Sipilä, Lea Puhakka, Leo Dunkel, Taneli Raivio	37
2	LIN28B, LIN28A, KISS1, and KISS1R in idiopathic central precocious puberty 2011 ·BMC Research Notes ·Johanna Tommiska, Kaspar Sørensen, Lise Aksglæde, (unknown), Lea Puhakka, Anders Juul, Taneli Raivio	36
3	A Novel Mutation of the Fibrillin Gene Causing Ectopia Lentis 1994 ·Genomics ·(unknown), A. H. Child, Katariina Kainulainen, Rebecca M. Davidson, Lea Puhakka, Leena Peltonen	70
4	Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome 1994 ·Nature Genetics ·Katariina Kainulainen, Leena Karttunen, Lea Puhakka, Lynn Y. Sakai, Leena Peltonen	195
5	Two mutations in Marfan syndrome resulting in truncated fibrillin polypeptides. 1992 ·Proceedings of the National Academy of Sciences ·Katariina Kainulainen, Lynn Y. Sakai, Anne H. Child, F M Pope, Lea Puhakka, Lasse Ryhänen, Aarno Palotie, Ilkka Kaitila, Leena Peltonen	100
6	Linkage map of the chromosomal region surrounding the infantile neuronal ceroid lipofuscinosis on 1p 1992 ·American Journal of Medical Genetics ·Irma Järvelä, Pirkko Santavuori, Lea Puhakka, Matti Haltia, (unknown)	13
7	DNA‐based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1) 1991 ·Prenatal Diagnosis ·Irma Järvelä, Juhani Rapola, Leena Peltonen, Lea Puhakka, Jouni Vesa, Pirkko Ämmälä, Riitta Salonen, Markku Ryynänen, P Haring, Aki Mustonen, Pirkko Santavuori	23
8	Confirmation of the chromosomal localization of human lamp genes and their exclusion as candidate genes for Salla disease 1991 ·Human Genetics ·Johanna Schleutker, Leena Haataja, Martin Renlund, Lea Puhakka, Juha Viitala, (unknown), Perttì Aula	3
9	Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1 1991 ·Genomics ·Irma Järvelä, Johanna Schleutker, Leena Haataja, Pirkko Santavuori, Lea Puhakka, Tuula Manninen, Aarno Palotie, Lodewijk A. Sandkuijl, Martin Renlund, R. White, Perttì Aula, Leena Peltonen	105
10	Infantile neuronal ceroid-lipofuscinosis is not an allelic form of batten disease: Exclusion of chromosome 16 region with linkage analyses 1990 ·Genomics ·(unknown), Lea Puhakka, Pirkko Santavuori, Tuula Manninen, (unknown), Leena Peltonen	7

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.

Explore authors with similar magnitude of impact