Concepedia

Author

Mikael Lindlöf

University of Helsinki

Also Known As

M Lindlöf, M. LINDLÖF, M. Lindlof, M. Lindlöf, MIKAEL LINDLÖF, Mikael Lindlof, Mikael Lindlöf, Mikael Lindlöf

30

Publications

1.6K

Citations

15

H-Index

37

Concepts

All Affiliations

University of HelsinkiVäestöliittoBaylor GeneticsInsermUniversity of Würzburg
ML

About

Mikael Lindlöf is an author at University of Helsinki specializing in medicine, molecular genetics, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

6

6

244

2

Public Health

2

2

49

3

Natural Sciences

1

1

50

4

Biostatistics

1

1

24

5

Child Development

1

1

25

Mikael Lindlöf

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15

Publications

1.5K

Citations

14

H-Index

YearCitations

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

Alan H. Beggs, Mary B. Moyer, S. Scherpf,

PubMed

1989

961

Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis

Albert de la Chapelle, Eeva‐Marja Sankila, Mikael Lindlöf,

Clinical Genetics

1985

77

Gene deletions in X-linked muscular dystrophy.

Mikael Lindlöf, A Kiuru, H Kääriäinen,

PubMed

1989

74

Erythropoietin Receptor Mutations Associated With Familial Erythrocytosis Cause Hypersensitivity to Erythropoietin in the Heterozygous State

Stephanie S. Watowich, Xiaoling Xie, Ursula Klingmüller,

Blood

1999

57

Carrier Testing of Children for Two X-Linked Diseases: A Retrospective Study of Comprehension of the Test Results and Social and Psychological Significance of the Testing

Outi Järvinen, Anna‐Elina Lehesjoki, Mikael Lindlöf,

PEDIATRICS

2000

53

242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread

Lau A.J. Blonden, P.M. Grootscholten, Johan T. den Dunnen,

Genomics

1991

50

Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families

Huw Dorkins, C. Iunien, Jean‐Louis Mandel,

Human Genetics

1985

49

Carrier Testing of Children for Two X-Linked Diseases: A Retrospective Evaluation of Experience and Satisfaction of Subjects and Their Mothers

OUTI JÄRVINEN, Anna‐Elina Lehesjoki, Mikael Lindlöf,

Genetic Testing

1999

25

Carrier testing of children for two X linked diseases in a family based setting: a retrospective long term psychosocial evaluation

Anna‐Mari Aalto, Anna‐Elina Lehesjoki, Mikael Lindlöf,

Journal of Medical Genetics

1999

24

Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.

Mikael Lindlöf, H Kääriäinen, Kay E. Davies,

Journal of Medical Genetics

1986

24

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